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#Science: How Scientists on Twitter & TikTok are Changing the Game

12/5/2020

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By: Eleanor Lin (CC '24)

On November 20, the Columbia Science Review hosted a panel discussion featuring three prominent science communicators: Dr. Esther Choo, Tyus Williams, and Dr. Rose Marie Leslie. Panelists fielded questions on how they are harnessing the social media platforms Twitter and TikTok to shape the dissemination and discussion of science. The panel was co-moderated by CSR OCM's Savvy Vaughan-Wasser (CC '22) and Everett McArthur (CC '23).


Panelists

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Tyus D. Williams is a wildlife ecologist. He received his bachelor's degree in Fisheries and Wildlife Sciences from the University of Georgia. He currently works as a field ecologist at the University of Nevada, Reno, with research interests including carnivore ecology. Through his Twitter account, @sciencewithtyus, and #SciQFriday, Williams communicates scientific content relevant to his own research expertise and interviews scientists from a diverse range of fields, engaging with an audience of 19,700 followers.
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Esther Choo, MD, MPH is a Professor of Emergency Medicine and Public Health at Oregon Health & Science University and a practicing emergency medicine physician. She is a cofounder of Equity Quotient, a board member at TIME'S UP, a columnist on healthcare inequity for the Lancet, a medical analyst for CNN, and a cofounder of Get Us PPE. She engages with 177,000 followers through her Twitter account, @choo_ek.
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Rose Marie Leslie, MD is completing her residency in Family Medicine at the University of Minnesota. In the past she has worked as a youth health educator. Her focuses include reproductive health, health education, and social justice. On TikTok, she is known to her 840,000 followers as the health influencer @drleslie, helping to spread accurate scientific information and combat misinformation.

Co-Moderators

Savvy Vaughan-Wasser is a junior in Columbia College ('22) majoring in Neuroscience and Behavior. Her love of animals and psychiatry is guiding her to become a doctor, with a possible intersection between animal and human medicine. Savvy has experience in a research lab studying cancer, as part of a research team geared towards fostering resilience and inclusivity for non-binary students in all-girls schools, and volunteering at animal hospitals. She enjoys archery, dancing, and anything chocolate.
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Everett D. McArthur is a sophomore in Columbia College ('23) planning to major in astrophysics. Currently, he’s involved in galactic dynamics research. In his free time he does public lectures in his hometown. He hopes that his efforts will increase scientific understanding in his community, as well as increase diversity in science. He enjoys long hikes, art, and playing the piano.

The panelists first fielded questions from the co-moderators:
Q: How did you get started in science communication?
Williams said, "I always loved talking about science, from the earliest days of my youth." He named biologist and wildlife conservationist Jeff Corwin as a key influence. The emergence of Twitter and Instagram, contemporary with his generation's coming-of-age, was another important factor in Williams's development as a science communicator.

Leslie's first role as a science communicator was as a peer health educator in high school. She noted the continuity between her past experiences as a health educator and her current training to become a doctor, which involves being able to convey information to patients in an accessible manner. 
  
Choo was a latecomer to social media. She recalled being an "extreme introvert" who used to shun public speaking. Choo first became active on Twitter at the urging of a friend (none other than former Surgeon General Dr. Vivek Murthy). Reflecting on past skepticism from peers who thought social media might be "a waste of time," Choo reflected that sharing academic publications via platforms such as Twitter is now becoming normalized, and that Twitter is an effective way to reach a broad audience in need of accurate information.



Q: How do you use your specific social media platform to convey your message to viewers?
Leslie said that one advantage of TikTok was the ability to easily integrate sound, music, text, video, and screenshots into posts: "You can create interesting, multimedia health education tips in 30 seconds." However, she stressed the importance of balancing the need to create engaging, interesting content against the need to base that content on scientific evidence from primary sources. Leslie said that she makes sure to highlight these sources in her posts.

Williams stressed the importance of being authentic and "meeting people on the same level" for effective scientific communication. He explained that he tries to build trust by being "as transparent as I can possibly be" and interacting one-on-one with his Twitter followers when they have questions or comments. In addition to Jeff Corwin, Williams pointed to David Attenborough and Jim Carrey as inspiration for how to inject his own personal character into his communication, including through humor.

Choo echoed the importance of authenticity and said that pre-COVID, she used Twitter as an outlet to discuss academic work in a more relaxed atmosphere. However, during the pandemic, Choo has experienced more stress while trying to coordinate with other health influencers to spread accurate information about complicated topics, such as vaccine trials: "Those are dry conversations, and yet we need broad uptake." 

While regretful of some missteps, such as flip-flopping guidance on face masks early on, Choo also noted that a lack of understanding of the scientific process—which requires recognizing and correcting mistakes—worsens the relationship between scientists and the public. Williams agreed with Choo that while changing opinions based on the emergence of new evidence is foundational to the scientific process, it is often negatively perceived by the public. Leslie had also posted about mask-wearing on TikTok using CDC guidelines, which had at first urged people to reserve masks for health care workers. When she reposted using the updated guidelines for universal mask wearing, she experienced a wave of negative comments. "I understand how frustrating it must be when recommendations change . . . or when scientists get it wrong," she said. Leslie used the experience as a teachable moment, subsequently making more content about how the scientific process works and how people can identify valid sources of information. 


Q: How can college students become better science communicators?
 Choo recommended that students find organizations and people they admire, then treat these as role models for their own communication. While students should aim to make posts accessible (Choo cautioned against posting screenshots of dense blocks of text), they should "always [be] going back to the science" by including links to primary sources. That way, Choo explained, the audience can read more and recapture some of the nuance which is lost in short-form tweets. Finally, Choo encouraged students to reflect on how becoming a prominent communicator might affect their professional and personal lives, disclosing that she and her family have received threats and been doxxed in reaction to her posts on controversial topics.

Williams concurred with Choo's words of caution, saying, "You are carrying everything that is representable about yourself in a way to be potentially scrutinized or applauded by people you don't know." He emphasized that communicators can prevent backlash by sticking to topics inside their area of expertise, but also said that students should be prepared for the fact that "even when you do get it right, people still come after you." Williams noted that his identity as "a Black man in science" and a 25-year-old has implications for how he presents himself and how people react to him. For example, some people have used his age as a basis to question his expertise. Williams concluded, "You have to be confident in yourself . . . But also protect yourself."


Leslie agreed with Choo and Williams that scientific communicators should be prepared to protect themselves from toxicity, including by differentiating between genuine scientific discussion and engaging with trolls ("Don't feed them"). Leslie re-emphasized that "being yourself is really important, especially if you're speaking to non-scientific audiences." Before posting, Leslie asks herself, "Am I creating this post with intention?" and "Would I be okay with one of my patients seeing this?"



Next, the co-moderators opened the floor to audience questions:
Q: How do you deal with social media fatigue? Has there ever been a point where you needed to take a step back?
Williams said that the key to preventing fatigue is to "listen to your body" and remember that the preservation of one's own health is a right. He shared that in the past year, he has been deeply affected by social upheaval in the United States, especially surrounding the deaths of George Floyd and Ahmaud Arbery.

Choo said that she structures her days so that she can spend time with her family and without the distraction of social media. Choo's philosophy is that social media should reflect one's larger life, rather than become one's entire life, and that fostering a healthy life outside of social media will naturally enhance one's ability to create good content.


Leslie admitted, "I am still trying to figure out how to manage everything I have going on" and that an important question to ask is, "Am I doing this for someone else? Or am I doing it for me?" The key indicator of fatigue for her is whether she is enjoying engagement with her audience, or whether it is starting to feel "like a job."



Q: How many times do you review a post before you send it out into the internet, knowing that every word will reach so many people?
Choo characterized her posts as "extremely spontaneous," because she sticks to posting about topics within her area of expertise, and therefore within her comfort zone. She estimated that she spends only "10 or 15 minutes" on social media each day.

Leslie agreed with Choo's distinction between posts within and outside of one's expertise, saying, "Make sure that you know your stuff before you post it."


Choo then initiated a discussion of panelists' favorite posts. Leslie chose a TikTok in which she dissected how to identify trustworthy and untrustworthy sources of medical information. Williams chose a post in which he analyzed the disproportionate amount of attention which non-scientist social media influencers can garner by improperly leveraging wildlife. In Choo's favorite post, she debunked false claims that George Floyd could breathe, using her expertise as an emergency medicine physician.



Q: How would you encourage student scientists to join the social media science community as either an audience member or influencer?
For Williams, the key questions are "Who am I? What can I offer? What do I enjoy the most?" He added that scientific communicators should show their audiences that they are not just scientists, but also regular human beings, using his own passion for rock climbing as an example.

"What do I have to say that isn't already out there?" Leslie urged aspiring communicators not to view this question as a barrier, but rather to recognize that their voice may reach certain people when other voices don't.


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Choo stressed the importance of developing as a scientist before becoming an influencer: "When in doubt, go back to the passion [for science]." She concluded by echoing Williams' advice to engage with the audience personally: "It takes being a little bit vulnerable."
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Zuckerman Brain Insight Lecture: Making the Right Moves in a PAndemic

11/10/2020

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By: Hannah Lin (CC '23)


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Dara Kass, MD, is an emergency medicine physician and Associate Professor of Emergency Medicine at Columbia University Medical Center. An advocate for women in medicine, she is a founding member of Time’s Up Healthcare, as well as the founder and CEO of FeminEM.



​Andrés Bendesky, MD, PhD, is Assistant Professor of Ecology, Evolution, and Environmental Biology at Columbia University and a Principal Investigator at the Zuckerman Institute. 
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Dr. Dara Kass began her presentation by sharing the importance of public trust during a pandemic. Over the past few months, she had been confronted with the significance of clinical decision making and leadership during uncertain times, and she reasoned that public trust required 3 things: honesty, humility, and humanity.

Honesty
At the start of the pandemic, there were many unknowns about COVID-19. This led to a flurry of guesses, instead of the usual time-tested, evidence-based communications scientists typically rely on. For example, there was not much evidence 6 months ago about the effectiveness of masks, and conspiracies started to arise. As more evidence started to emerge supporting mask-wearing, these conspiracies were disproved, but they still lingered, since there wasn’t much space for evolving information. Honesty provides this space, Dr. Kass said, and people need transparency.

Humility
Doctors need to be open to feedback and admit mistakes. Trust is cumulative, and if any interactions with the public go wrong, their perceptions of truth can also be affected, Dr. Kass said. 

Humanity
Dr. Kass emphasized the need to be sensitive with people, and to be sensitive yourself. Dr. Kass, who was infected with COVID-19 earlier in the year, made the conscious decision to be public with her symptoms and her anxiety online, normalizing the feelings that many others were experiencing. Noting the health disparities made apparent by the pandemic, she ended her talk by emphasizing the need to incorporate human feelings into public messaging, focusing on the ultimate goal of collective unity.

Dr. Andrés Bendesky began by explaining the lack of appropriate and adequate testing of who exactly was sick and who was contagious at the beginning of the pandemic. Much contagion occurs before the onset of symptoms when the viral load is at its peak, and the symptoms themselves were variable from person to person. For medical and epidemiological purposes, a more sensitive test is needed; the PCR test is an example. Meanwhile, for determining whether a person is infected or not, a less sensitive test is sufficient; for example, a rapid antigen test. To best combat the virus, daily testing has the highest ability to remove infectiousness, but issues arise with the lag of time after a test and the lab equipment needed to produce a result. 

With volunteers, he formed an interdisciplinary team to develop a simple, affordable COVID-19 test. Their idea came about through LAMP (Loop-mediated isothermal AMPlification) testing, where only one tube and a constant temperature were needed. Using specific chemical reagents, test-takers could simply input their saliva, and the resulting color of the tube would indicate whether they were infected or not. With an easy-to-use apparatus, the ease of this test has huge advantages for everyday usage, and Dr. Bendesky reported the validation of his lab’s work by testing people with varied viral loads. 
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After the speaker’s presentations, Natalie Steinemann, PhD, moderated the discussion with some questions from the audience. One frequently requested topic was immunity and vaccines. The speakers noted that, based on preliminary data, the COVID-19 vaccines in progress seem to have a high effectiveness. 

A question arose about the possibility of a disturbance of the COVID-19 vaccine with the flu vaccine, but Dr. Bendesky noted that combining vaccines is actually normal: many young children get multiple vaccines at a time. As of now, there are no signs that there would be a disturbance between the two. Dr. Bendesky also noted that although there have been some mutations of the virus, they have not had large impacts on the ability to form a vaccine, unlike with HIV.

As for air travel, indoor dining, and family gatherings, Dr. Kass said that air travel looks to be relatively fine due to the diligence of passengers, mask mandates, and air filters. Indoor dining, however, is dangerous when the tables are too close and guests are dining with people that they don’t usually interact with, which could facilitate the spread of the virus. Home events, if necessary, should be capped at a minimal number of people to maintain safety.

To help out in your own communities during this time, Dr. Bendesky talked about finding your strengths and using them to your advantage, as well as being creative with your efforts. Of course, the best thing you can do is follow all public health guidelines, making sure that you are not transmitting the virus.

Dr. Steinemann finished by asking the speakers whether they were hopeful for the future. Dr. Kass and Dr.  Bendesky both answered positively,  inspired by the unity that New Yorkers showed during the pandemic. They hoped that new leadership, better communication, and transparency about the pandemic would be successful in uniting our communities and combating the virus.
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The World’s Leading Expert on the Seasonality of Infectious Diseases Takes on COVID-19

8/4/2020

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By: Hannah Lin (CC '23)

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Cover illustration by: Arooba Ahmed (CC '23)

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Micaela Martinez, PhD, is an infectious disease ecologist and an Assistant Professor of Environmental Health Sciences at the Columbia University Mailman School of Public Health.


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​You’re an infectious disease ecologist in the field of environmental health sciences. That isn’t your typical biologist or chemist. Could you explain what your title means, and also what your personal and professional path to this field looked like?


As you mentioned, I’m an infectious disease ecologist, and there are only several hundred of us in the world. Those of us that identify as infectious disease ecologists are people who typically have PhDs in ecology or evolutionary biology, oftentimes also applied mathematics, and who essentially study infectious diseases from the lens of ecology and evolutionary biology. 

You can think of infectious diseases as predators, except they have much smaller bodies than their prey. So many of the same types of population level principles that have been used for fifty, eighty years now to investigate predator-prey relationships have now been applied to infectious diseases. Much of the same mathematics that’s used in, say, fisheries biology or predator-prey population dynamics, we apply that to infections. 
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Most of my work and the work of other disease ecologists is focused on the population level -  how pathogens transmit through populations. For instance, I’ve done a lot of work on eradication and elimination of things like polio and measles. You can essentially think of eradication initiatives as the flip side of conservation initiatives. Ecologists that work in conservation biology figure out what we need to do on a population level to make sure species don’t go extinct, while we do the opposite of those same things with infectious diseases on the population level to drive pathogen species to extinction. 
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That’s kind of the framing of the science. We also use evolutionary biology to study either the biology of the host, which is what my lab does in our approach to the immune system, or also the evolution of pathogens themselves. Many disease ecologists also look at the evolution of things like flu and HIV through the lens of natural selection, which is something all species experience, particularly looking at it from the disease angle. So that’s disease ecology as a field. 

In general, I’ve always been an ecologist. Well actually, I first started out in a genetics lab doing more evolutionary work with fruit flies. Then I moved to doing field work and endangered species work with Arctic seals, so I was working on the endangered species listing for ringed seals, which are the primary prey of polar bears (when you see pictures of a polar bear pouncing on seals, it’s those seals I used to work on). 

Because I was studying both mathematics and biology, I wanted to be in an area that was very mathematically leaning. In ecology, the two areas in which there is a lot of modeling applied are infectious disease work and fisheries work. I went the infectious disease route so I could use my math skills. From there, I just got really interested in working on childhood infectious diseases, did my whole PhD on polio and measles, then subsequently did work on other childhood and early life infections like chickenpox, and also worked on Zika for a bit once Zika emerged. 

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Now, my lab has also started to study biological clocks. You’re probably familiar with circadian rhythms, our 24 hour body clock, but now we’re addressing whether or not humans have a seasonal body clock that goes along with the seasons like other mammals do. As you're probably aware, a lot of mammals have their offspring in the springtime, so they have very distinct breeding seasons. Many species will change their coat color throughout the year and/or migrate, hibernate. All of those seasonal processes have a basis in a seasonal clock, which pays attention to the changes in daylight. 

The last several years, my lab has also been funded to see if we have seasonal changes in our immune system that influence when we get sick and if the basis of this is a seasonal biological clock. That’s the other area of my research. I think that type of work makes a lot clearer the types of things I study as a disease ecologist. From my perspective and just in general, humans are just another mammal, so we can ask the question: how does the fact that we’re just another mammal play into our health and wellbeing?


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Jumping into your COVID-19 related research now, from what I saw, you and your team have been studying the immunology and transmission of this pandemic. Could you talk about your work thus far?

In terms of COVID, my work has fallen into three distinct projects. 

One of them, which I would say is most closely aligned with the other work in my lab right now, is looking at the immune system during COVID. It’s quite clear that it’s the immune system that is doing the majority of the damage in individuals who are hospitalized, severely ill, and may succumb to the infection. For some individuals, what happens is the immune system is over-reactive and has an incredibly inflammatory immune response. Our immune system has the ability to react very strongly to an infection, but we also have processes in our immune system that keep it in check, that harness it in and don’t let it get too bonkers. But on occasion, what happens is those regulatory processes that would usually manage your immune system can fall apart for many reasons, which for COVID-19 seems to be the case. The inflammatory response just spirals out of control to such an extent that individuals can get what we call immunopathology, where you have pathology, or harm, that is being done to your body by your immune system, including things like tissue damage in the lungs, which can make people have ARDS (acute respiratory distress syndrome) and be put on a ventilator. 

So my group and collaborators, a pretty good size group of us, have been working on this. As more and more data becomes available from the immunology literature, what we’ve been trying to do is puzzle-piece all of these studies that might be looking at one or two aspects of the immune system at once or the clinical progression of the disease. We’ve been trying to puzzle-piece all of this together to say, okay, what is happening through time in the immune system, and how is that being followed with symptoms of severe disease? 
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Our hope is that now by scouring the literature, by integrating data from different sources, and by digitizing data that become available (and now we’ll be using clinical data from Mt. Sinai and Columbia), we can come up with predictors for markers of our immune system that are predictive of what path the person will follow. If someone ends up in the hospital and you take a blood sample from them, we would like to be able to predict with some probability, what the chance is that this person is going to be, say, hospitalized for a week or two, recover, and be discharged versus need to be put on a mechanical ventilator and either go down the path of continued tissue damage and potentially death. 

As of right now, all of those paths are just dictated by your immune system. There’s not much that is able to be done on the care side of things to dictate people’s pathways that they take. Ventilators are just trying to minimize the amount of tissue damage that’s being done by helping the body supply oxygen, but they are not actually helping heal. The whole process of healing is a process of the immune system as well. 

The second project I have going on is transmission modeling for New York City. There are lots and lots of modeling groups worldwide that have been constructing transmission models for COVID. Where my group differs from some of those other groups is in two areas. 

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One, we want to do more long term modeling and projections based on how our immune system will respond to the virus. Right now, it’s still unknown whether or not we’re going to have what we call sterilizing immunity. Once you get infected, is that going to protect you from subsequent infections? And is it going to protect you perfectly, or is it going to protect you with some efficacy, or is it going to not protect you from infection but maybe protect you from
severe disease if you get infected? There are all these unknowns, so we need to be able to run scenario 
analyses for all these unknowns for the immune system and what’s going to happen. We need to model into the future and say, okay, if our immunity works this way, then this wouldn’t happen. If our immune system works this way, then this scenario would happen. It’s kind of like when you think about climate change scenarios: if we cut down carbon emissions this amount, then we project this will happen. Same kind of deal, but for the immune system. ​ ​

Also, I’ve been working with the air pollution scientists in my department to come up with a way to measure social distancing and the slowing down of cities on lockdowns. You can easily come up with a policy; for example, the governor’s policy for lockdown in New York State where people were told to stay home. But to actually quantify and measure that is really hard unless you have something like proprietary cell phone data from every person and you can see where they’re going. 
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What we’ve been doing is creating algorithms to scrape Google Maps data. If you pull up your phone and you pull up Google maps, it’ll show you the roads and the traffic, and it’ll color code the roads red for heavy traffic, dark maroon for the heaviest traffic, green for free flowing traffic. Well, the way that Google actually gets those data is by tracing the movement of people’s cell phones, so Google Maps is, in a way, representing all that cell phone data that we don’t 
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have access to. We’ve been generating algorithms that will go and take snapshots of Google Maps for every neighborhood in the city, and then puzzle-piecing those together to see how much movement there is around the city on fifteen minute intervals, going from pre-pandemic to now. We know via this type of publicly available data mining how much movement there is around the city, which can, in some ways, be a proxy for transmission potential. ​

My last COVID project is work that is under review right now and should be published shortly that looks at the socioeconomic and racial disparities in social distancing. When we look at the disparities based on race and ethnicity for COVID-19, there are essentially two sides of it. 

There’s first, thinking about what the probability is that an individual acquires the infection, and that's going to be largely dependent on how much infection is in their community, their ability to socially distance depending on what type of work they do, and also housing: if they live in a multigenerational household or if they live in a household where, if an individual is infected, they can stay away from other household members and quarantine effectively, that type of thing. So there’s that transmission side of it. 

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Then the other side of it is if you are infected, contingent upon infection, what’s the chance that you’ll have very severe disease? We also know that there are disparities on that end as well, and in New York City, if you are a Black or Brown New Yorker, you’re a little more than two times more likely to die of COVID-19. 

So we’ve been trying to tease these two components apart, and some of the work we’ve done is looking at the social distancing inequity where we found that if you break down New York City by neighborhood and you look at the demographics of that neighborhood in terms of 
race/ethnicity, percent of essential workers, median income, and you can also get things like education, all of these things are very tightly correlated within New York City and, I would say, more broadly in the United States. If you’re poor, you’re more likely to be Black or Brown. If you’re poor, you’re also more likely to be a lower-wage worker that has to leave the home in order to work. You don’t have the luxury of staying home. All of these things come together to shape, at a community level, how much transmission there is in the community and at an individual level the risk that people face. ​
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​We were able to show some of this using subway data in New York City because we were able to get the number of subway swipes at every single turnstile in the city and we know where each turnstile is geographically. What we found is that in the richest neighborhoods in New York, the decline in subway use during the pandemic and during the shutdown was the most extreme. And as you look at neighborhoods that are lower income, they also had declines in subway use, of course, because everything was shutting down, but not as stark of a decline. We termed this social distancing inequity because we presumed that people going onto the subway during the middle of the pandemic is not by their own choice, it’s out of necessity. 

So we tried to bring data together on race/ethnicity, socioeconomics, and the movement in subway use during the height of the pandemic to try to tease apart what was happening. Overall, we found that neighborhoods with 
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higher subway use during the pandemic also had higher incidence of cases, and we believe this is because of community transmission because of the social distancing inequity that's faced.




What are the broader goals of your research? Do you want to provide models for policymakers when reopening cities or something else?

This is one thing that is really interesting. For instance, using the models that we’ll have for New York: inevitably, yes, policymakers are going to pay attention to that, but I’m not really in the business of modeling for policy. I’m much more in the business of modeling to understand fundamental biological processes with the aim that understanding the underlying biology will then inform translational medicine and policy. 

In reality, the type of work that I do, since it is more biology focused, is not meant for rapid action. If I were wanting to inform policy very directly, then I would be doing different types of modeling: for instance, modeling what the optimal criteria for shutdown and reopening would be or if you wanted to do cocooning for at-risk individuals, how you would stratify populations so some people would stay home, some would go to work, that kind of thing. Those are very directly applicable policy things, whereas my work is much more long-horizon, informing biology. 


​

As you said earlier, prior to COVID-19, you were researching other infectious diseases like polio and measles. How was the transition from researching those to this current pandemic, and did your experience with those give you unique insights into COVID-19?

Yeah, definitely. The thing is that I’ve been working on the biology of acute infections for so long and coming at them from a biological angle, so it’s not all that different. COVID is just another directly transmitted infection. There is a playbook for infectious diseases. Like I was saying with predators and prey, infectious disease systems behave a certain way. There are biological bounds to how they behave. 

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My work on other pathogens very directly allowed me to work on COVID and in some more nuanced ways, because particularly with my work on polio, polio is also an infection where the majority of the infections are asymptomatic, so they’re not showing symptoms. The types of modeling frameworks that you would have to employ to be able to work with that type of a disease system is something that I specialize in. These are what we call partially observed systems, where you can’t observe all the infection, you only observe a little drop in the bucket. That means you have to be very careful with the types of model structures and data interpretations. That definitely made a big difference in terms of how I differed from, let’s say, epidemiologists that would work on these systems.

I think I can say now that I’m the world’s expert on the seasonality of infectious diseases - that and seasonal clocks, biological rhythms in humans, are the two things that no one ever studied. Before COVID, there were so few people in the world that had any interest in seasonality of infections, and even fewer people who had ever done real empirical research in that area. 

When COVID hit and you had things like Donald Trump saying, “it’s going away as soon as it gets to summertime,” it was like every reporter was emailing me. I think I was uniquely placed even compared to my close colleagues because I realized I had spent so many years thinking about it that I just very innately know the nature of seasonal disease dynamics, and the math behind it is very ingrained in my brain. I noticed it with my colleagues when I thought they had the same skill set as me, but because they hadn’t specifically worked on that one area, they weren’t as well placed to think about that for this new infection. I would say my seasonality work made it so that as soon as people were asking if it was going to go away in the summer (I even had some other disease people who I would hear have that hope), I was like, no, you guys, no! I think I had just thought about that problem for a lot longer than other people had. 




Is there a reason why biological rhythms and seasonality haven’t really been extensively studied?

There are a couple things. First of all, in terms of biological rhythms, the reason that hasn’t been studied very extensively is because it takes a really long time to study things that happen on a yearly basis. I even did an international talk a couple weeks ago on seasonal rhythms, and there were five of us speakers. The person who gave the introduction to the session said: okay, now we’re going to talk about circannual clocks (which is the seasonal body clock), and she said: this is the area of biology that has been termed “where biologists come to die.” It’s because it takes so many years. If you’re looking at a process that takes a year to happen, just to observe it twice, you have to take two years. And because of the way that biology is, all fast 
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pace, getting papers out, getting grants, and such, there’s no incentive for anyone to spend their career on that unless they’re just really intellectually driven by it, which is why I worked on it. ​

For infectious diseases, the seasonality is very, very obvious in any infectious disease data that you look at. I would think that one of the reasons that people hadn’t studied it could just be that people don’t look at ubiquitous things, maybe? When something is so common, people don’t realize that it’s very interesting: it’s just like, the earth rotates around the sun and is tilted on its axis, so of course we have seasons! I think it’s one of those things that, since it’s so common, it gets overlooked.




Lastly, what is your perspective on the future, and for a note of optimism, what gives you hope for the future?

I’ll give you the good and the bad. My perspective overall is that with global climate change and the widespread destruction of natural ecosystems, including land use change and deforestation, humans, especially over the last 200-300 years, have done what is pretty close to irreversible damage to our planet. If I were just to say very bluntly, I think this pandemic has been a slap in the face from the earth to human beings. 

Humans have notoriously been going into natural spaces for so long where we don’t really have any business to be in. It includes forcing novel contacts with species that we usually don’t interact with. In the past, this has posed problems for us, like having zoonotic diseases that have moved into humans - things like all of our flu viruses, Ebola, HIV. But I think that in the past, there have been very few things that have just gone straight from jumping into humans right to a pandemic. Also, some of the past emergences were either more localized or they happened during a time when we didn’t have such widespread global connectedness, in terms of social media, news. 

Now, all of a sudden, it’s an age-old problem (age-old meaning industrial age-old): humans going places we shouldn’t be, we have a spillover from hosts into humans, and now we have this pandemic. But everyone is aware of it now, and there have been huge economic consequences and loss of life in a very short amount of time. 

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I think this has a potential, if I’m to be very optimistic, to globally awaken society to the fact that we have not been stewards of our environment as I believe that we should be, given the fact that we have such heavy resource use and that we have expanded into essentially all parts of the globe. We’ve been told and have known for quite some time that if we continue down the path of widespread extraction of natural resources without any caring or management and pumping greenhouse gases into the atmosphere, there would be dire consequences for us. But for the most part, those consequences haven’t been very readily in our face, unless you’re someone who perhaps lives in an island nation and you can see sea level rising and the loss of your land or if you live in a desert nation where you see more drought, you see desertification and climate refugees. There are places that are feeling that, but in a lot of the world’s worst polluters and global powers, people are not seeing it as readily, so they’ve been able to ignore it. 

I think that this is going to be a turning point where either, optimistically, people realize we need to be stewards of our environment and pay attention to these things, that our actions have consequences, and therefore become those stewards that we should be, tackle climate change, tackle land use change, think about widespread extinction and pollution of our environment. And if COVID doesn’t do that, I really don't think anything else will. There’s really not much more of an acute shock that you can have from the environment onto humans than this. So I do think it does have the potential to be a turning point, but we’ll see.
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Studying Psychological Distress in NYC Healthcare Workers During COVID-19 With Marwah Abdalla

7/24/2020

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By: Hannah Lin (CC '23)

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Marwah Abdalla, MD, MPH, is an Assistant Professor of Medicine at Columbia University Medical Center, Director of Cardiac Intensive Care Unit Education, and a faculty member at the Center for Behavioral Cardiovascular Health at Columbia University.



Can you introduce yourself, your titles and affiliations, and talk a bit about generally what work you do?

My name is Dr. Marwah Abdalla. I’m an Assistant Professor of Medicine in the Division of Cardiology, I’m a clinical cardiologist and a clinical researcher. My areas of expertise include critical care cardiology, and I’m the director of education here in the cardiac intensive care unit. With regards to my research expertise, I work in hypertension and sleep.


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Shifting now to your work regarding COVID-19, you were the leader of a study which characterized psychological distress and coping among New York City healthcare workers during the peak of the pandemic, the largest such study done in the US. Could you talk about when and why you decided to research this?

This all came out from my experiences taking care of patients during the pandemic. I had the privilege of serendipitously being in the cardiac intensive care unit as the attending during the first week of the pandemic when it hit New York and when the very first case came through the doors of New York Presbyterian. So it was an interesting and serendipitous opportunity where everything came together very, very quickly with regards to what the questions were that needed to be answered. You can imagine that during the first week of the COVID surge, there were so many unanswered questions. There was also a lot of uncertainty amongst family members, patients, and the staff as to what this new pandemic meant. 

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It was just my observation, while taking care of some of these patients, that this disease is very different in that for the very first time, there was this merging of both patient care and a public health crisis at the same time with huge ramifications for people outside of the healthcare world. I  noticed that there was a lot of uncertainty and many new types of questions that were raised in rounds and this felt very different, it felt people were really struggling with this pandemic in a way that goes above and beyond anything I had seen before, and I thought that it would be important to understand what the psychological consequences would be of going through this pandemic for the healthcare field in general. 

​That’s really where the idea came from: the observations on the ground during the very first week of the pandemic and saying, “This is going to be here for a really long time. How can we help not just our patients but also really ground ourselves and be helpful to our colleagues who are taking care of those patients?”




Just running through some statistics from the paper, fifty-seven percent of participants screened positive for acute stress, 48% screened positive for depressive symptoms, 74% had concerns of transmitting COVID-19 to family, and 80% reported engaging in at least one type of coping behavior, with physical activity being the most common. Were there any responses you got that surprised you, or were they relatively close to what you expected?

I think this paper and the data definitely highlighted what our hypothesis was going to be, that there were going to be a lot of people who had acute stress syndrome and fears about transmission. At that point in time, in early April, when we launched the study, there were still questions about N95s and whether people should be masked or not masked that were part of a national conversation. There was a lot of fear about transmission, and a few colleagues who were frontline healthcare workers actually got sick, and some, unfortunately, passed away subsequently from that. The national discourse was about that, so I think that was not surprising. 

I think it was great to see that there were so many people who were actively trying to think about their own wellness and using coping strategies, so that was encouraging. Even in this very tough scenario, people were taking time to take care of themselves. I think what we were surprised about was that 61% of our participants had optimism and an increased sense of meaning and purpose, which I think was 
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really remarkable and it goes to show how much healthcare workers, even in the midst of a crisis, are finding new meaning and thinking about how they can collectively work together to beat this pandemic. So many people were collaborating and trying to think quickly and change in such a way that was really refreshing. ​




In the paper, it says participants were given the choice to enter a longitudinal follow-up for up to 3 months. Could you talk about your progress on that?

Our participants are still part of the study and we'll be completing it soon. The last participants are finalizing their study responses. We have not yet analyzed that portion of the data, where our goal is to understand what the long term effects of the pandemic are on our healthcare workers who were so gracious to fill out the first portion of the survey. Do our participants continue having acute stress months out, is it limited to just the peak of the pandemic and things get better, or is it that people are still struggling while other things pop up as the months go by? 

I think that’s an important thing to understand as we figure out how we best support healthcare workers during any sort of public health crisis, but particularly for COVID-19, since it’s still an ongoing international crisis. We need to prepare ourselves to help others who may be going through the pandemic and say, “This is what you may expect in your own healthcare workers.” I think those are important conversations to be had. Obviously, our study results are limited to our New York campus, but I think there are elements that are probably shared since it’s an international pandemic. In China, a study showed that healthcare workers during COVID-19 actually do have signs of psychological distress, and we don’t know how far this distress stays with individuals. 




The paper also says that your findings highlight the need for rapid interventions to reduce psychological distress in healthcare workers. Have you seen any of those rapid interventions put into action?

Actually, while we were launching the study, what was great was that both Columbia University and NewYork Presbyterian implemented wellness resources for healthcare workers. All our participants had access to wellness resources during the study because we thought it would be unethical to just collect information. It’s been great that on campus, there’s been an understanding of the fact that healthcare workers during a pandemic need this extra support. 

What we’re really trying to highlight is that for other institutions and organizations for which there may not be access to the same resources that our healthcare workers had, they might want to consider having this in place. We want healthy healthcare workers; the wellbeing of healthcare workers have to be at the forefront of organizations that are going through the pandemic. 

As you may or may not know, there have been several national organizations now that have developed free psychological resources for healthcare workers who need that support, so I’d say that even if an organization within the US may not have the resources themselves, there are other resources that are available for colleagues and that’s been great to see develop as a result of the pandemic.




For students interested and inspired to go into medicine or research, especially in your specialities, do you have any advice or life lessons that you’d like to impart?
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I think for students who are interested in medicine and public health, and especially research, keep asking questions, learning as much as you can, and really try to spend time in clinical spaces if possible. There’s a difference between learning medicine versus practicing medicine, and for me, what was always inspiring and rejuvenating was being able to be with patients and having that opportunity to interact with healthcare workers, nurses, advanced practice providers, attendings, the whole gamut of healthcare. That was really motivating while going through my own journey and learning as much as possible.




I always like to end with some optimism: what gives you hope for the future? 

It was really humbling to see over the past couple of months how quickly the world came together to try to beat and find solutions for COVID-19. There continues to be hope, especially in the scientific community and the public health community, that we can come together and figure out how we can move forward to combat COVID-19. That gives me a lot of hope.

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Public Health Messaging in Minority Communities and COVID-19’s Neurological Effects With Hiral Shah

7/22/2020

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By: Hannah Lin (CC '23)

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Hiral Shah, MD, is an Assistant Professor of Neurology at Columbia University.



Could you talk a bit about the work that you do?

I work in the Department of Neurology and in the Division of Movement Disorders, so I mostly focus on seeing patients who have degenerative diseases such as Parkinson’s Disease, Huntington’s Disease, and others. My research focus is centered around public health approaches to improving access and treatment for neurological disorders. In that capacity, I also work as a consultant for the World Health Organization.



How did you get started in public health research and neurology?

I think for me, like many of my colleagues, my interest in neurology began as a medical student when I was doing a rotation with a particularly dynamic neurology attending who inspired me to pursue this line of work. I’m fascinated by the brain and its workings, so that has always been the scientific base for my interest. I’ve also always had a passion for public health and trying to examine the problems that we all face in our communities and how best to tackle those issues, but using a public health perspective rather than bench science or other approaches. With that, it was a 
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little serendipitous that I had the opportunity during my training to work at the World Health Organization and really observe firsthand how public health initiatives can transform care delivery in a variety of ways.



From what I saw, your COVID-related research focuses on health disparities for Black and African American New Yorkers. Could you talk a bit about that?

Here in New York, the initial epicenter of the COVID-19 pandemic, we observed firsthand the egregious health disparities which were further highlighted in the context of the pandemic. Though we suspect that social determinants of health and a multitude of factors such as issues related to education, housing, insurance, health literacy, and structural racism all have played into the more severe outcomes and the brunt of the burden of the illness being borne by our minority communities, I still think that there is a lot left to be learned in terms of what the modifiable risk factors or modifiable barriers are that, as clinicians or as public health experts, we could try to leverage to improve our response to the pandemic, both now and in the future. 

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So with that in mind, my hypothesis was that these minority communities, because of their social determinants of health, but also perhaps because of issues related to lack of trust or stigma, were not having the same rates of uptake of public health messaging as other communities and that this may be a point of entry for researchers and policy makers to attempt to modify our approach for these communities and offer a more tailored solution. 

We have launched several surveys looking at the ability of various communities to adhere to social distancing guidelines, as well as other aspects of public health messaging, to better understand our communities and gain knowledge of the COVID pandemic, its risks, 
and related myths surrounding the disease that could shed some light on ways that we could improve the health of these communities. ​



How is your progress on these surveys? Are you still collecting responses?

We’re in the middle of collecting data, and we also wanted to be mindful of ensuring that we’re capturing this information in a way that’s acceptable to these communities. We took special steps to partner with community- and faith-based organizations, such as St. Luke A.M.E. Church, to get their input on the survey at the developmental stage, and they’re also assisting us in terms of dissemination of the survey. We’re planning to both have the survey be available over the Internet as well as over telephone, because certainly, access to technology is another barrier in this day and age when in-person research as well as in-person clinical care are quite limited given everyone’s fears surrounding coming to the medical center.
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Where do you see your research going in the near and far future? I know you talked about the broader goals of having your work reflected in public policy as well as community and institution-level strategies.

I think in the near term, within our department, we may be able to modify our messaging and the way that we educate the public in terms of safety and coming back to the medical center. In the era of the COVID-19 pandemic, we’ve also observed that many are reluctant to come seek routine care because of fears related to COVID, so I think if we can better understand what those fears are, which is part of the survey, then we can better address those concerns to ensure that there aren’t unnecessary delays to care that further cause negative health consequences for our communities. 

In the long term, I think that we simply don’t know enough about the effective strategies to reach minority communities. Sometimes, simply translation of messaging is used to communicate with Hispanic communities, but I think that we need to think more creatively and out of the box in terms of how we get these public health messages out to the community, whether it means relying on local faith leaders that are based in the community or using mass media or alternative approaches. I think we need to think outside of the box in the future because clearly, public health messaging has been a little inconsistent throughout the pandemic, which has led to more confusion for the public on how to respond and what guidelines to follow. I think we need to think of novel ways to reach minority communities and provide messaging that’s a little more tailored and culturally appropriate.



Switching gears to your clinical work: obviously, you not only do research, you’re a neurologist as well. Could you talk about your experience as a neurologist during the pandemic?

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As neurologists, and I think many practitioners, we’ve transitioned to providing the majority of our healthcare using telemedicine. I think neurology lends itself well to this care delivery modality, because we often make a majority of our assessment based on the physical examination, which through video, we are able to do. 

However, I think that for many of our patients, it’s also been fraught with challenges, including access to the technology itself. Some folks simply don’t have access to a smartphone or a device that enables video conferencing to facilitate a telemedicine visit. In addition, some of our patients have mobility or cognitive deficits, so they have 
challenges with using the technology and positioning themselves to allow for an appropriate examination.  And, many of our patients are older adults; I think we all know family members or friends ourselves who struggle with these new technologies and how to implement them. So though I believe it’s been an exciting time in which we’ve been able to take advantage of and leverage telemedicine and information technologies, I think it’s also exposed a lot of the barriers to its implementation universally.



In terms of COVID-19 infection, we’ve heard a lot about the respiratory and cardiac effects. Could you talk about the neurological effects?

Absolutely. The neurological manifestations of COVID-19 have been of great interest. I think at the onset of the pandemic when it became obvious that anosmia, or lack of sense of smell, was a feature of the disease, that got a lot of people’s attention. It’s thought that the virus likely gains access or entry into the neurological system by the mucosal membrane in the nose and that maybe travels to the brain in that way, but this has not been confirmed. 

There have been a lot of studies looking at whether we can find virus in the brain tissue or the brain fluid, but those results are limited. We do see a lot of patients that have neurological manifestations of the disease including confusion, seizures, and strokes, due to the vasculature, the blood vessels, in the body becoming affected. There are other less common manifestations where we’ve seen brain tissue destruction, but more rarely. I think it’s still a question for study and a reason why COVID-19 has been such a challenging virus to deal with, because it does seem to affect so many different organ systems in a profound way. We continue to learn, based on pathological samples and brain tissue, what the impacts of the virus are on the brain.
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For students out there who want to pursue a career in neurology or public health research, do you have any advice or life lessons you’d like to impart?

I would just say follow your passions and your interests. Always look for ways that you can get involved. I think learning on the job or on the ground, so to speak, is one of the best ways to figure out whether it’s really something that interests you and something that you want to pursue as a lifelong career. I would encourage students to try to find opportunities and get involved.



Both regarding science and research as well as society at large, what is your perspective on the future, and what do you want the future to look like?

That’s a big question. I think that this period of time has really opened a lot of eyes for folks in terms of the egregiousness of health disparities and how that impacts some communities more than others. I just hope that it leads to more awareness and activity to try to tackle those problems, because I think that these problems have existed long before the pandemic and will continue long after. Perhaps with additional attention and interest, we can really have some more momentum to solve some of these issues, because I think if they are prioritized and recognized for the terrible consequences that result, we can all really work together to make a change and improve the health of our minority communities in particular. I think that that knowledge will translate to improving the health of our communities at large. 

Thanks, Hannah, for taking the time to speak to me!  
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The Impact of COVID-19 on Transgender and Nonbinary Americans with the Project AFFIRM Team

7/20/2020

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By: Hannah Lin (CC '23)

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Cover illustration by: Zoe Chan (CC '22)

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Walter Bockting, PhD, is Co-Director of the Program for the Study of LGBT Health, Professor of Medical Psychology (in Psychiatry and Nursing) at Columbia University Irving Medical Center, and Principal Investigator of Project AFFIRM.
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Kasey Jackman, PhD, RN, PMHNP-BC, is a Postdoctoral Research Fellow at the School of Nursing and the Program for the Study of LGBT Health at Columbia University, a psychiatric nurse practitioner, and a researcher at Project AFFIRM.
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Jeremy Kidd, MD, MPH, is a Research Physician at the Research Foundation for Mental Hygiene, Columbia University Irving Medical Center, and a researcher at Project AFFIRM.
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Renato Barucco, MS, is the Program Coordinator of the Program for the Study of LGBT Health, a psychologist and public health advocate.


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Can you introduce yourselves and what work you do?

RENATO BARUCCO: My name is Renato Barucco. I’m the coordinator of the LGBT health program, so I coordinate all the different projects of the program across psychiatry and nursing under the direction of Dr. Walter Bockting and Dr. Anke Ehrhardt.
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For this COVID project, I worked with Jeremy in terms of selecting participants that were eligible to participate in this survey, and that was most of our cohort in New York, Atlanta, and San Francisco. For this part of our study, we only surveyed English-speaking participants. Then, my role was also to make sure that participants received compensation after they participated in the survey. 

I’m currently doing a qualitative analysis of the open-ended question portion of the survey. There were about seven questions where we asked participants to tell us more about some of their struggles during the pandemic. We realized that a lot of 
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people gave us a lot of information in their answers, so we thought it would be important to do a qualitative analysis of these answers. That’s what I’m doing right now.
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WALTER BOCKTING: I’m Walter Bockting. I’m the principal investigator of the overall study, Project AFFIRM, a longitudinal study of transgender identity development across the lifespan. We have been following participants for over three years. It was Jeremy’s idea during this COVID time to contact them again.

It wasn’t initially planned, this was a bit of an expansion. Normally, we have people come in for interviews, and they’ve done that three times: baseline, one year, and two year followup. This time, it was fitting, given the social distancing, to do an online survey instead to see how our transgender people in the three cities that Renato mentioned are coping with COVID-19.

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JEREMY KIDD: I’m Jeremy Kidd, he/him. I’m an addiction psychiatrist, and when I started this project, I was a postdoctoral research fellow at Columbia University and New York State Psychiatric Institute in the division of substance use disorders, but I’m now transitioning into an assistant professor role at Columbia.

I’ve worked with Walter since coming to Columbia in 2013 on some sub-projects within the AFFIRM cohort, and a lot of the work that I am transitioning into doing is looking at social support and the role that social support and gender affirmation play in mitigating some of the negative health outcomes and health disparities that we know occur for trans and gender nonbinary folks. 

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I also do a lot of clinical work, and I was hearing from a lot of my patients the difficulties they were having with physical distancing that turned into social distancing and social isolation, so I thought it would be interesting to go to our cohort and hear from them about what this experience has been like for them. It’s been very interesting to see the way that people have really utilized that opportunity to share with us what their experience has been like. Even in the process of speaking with people on the phone to get them to fill out the survey, we’re hearing from people about how difficult this period of time has been for them. For people who were already having a really difficult time in their lives, this pandemic compounded that.


KASEY JACKMAN
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My name’s Kasey Jackman, I use he or they. I’m currently a postdoctoral research fellow at Columbia School of Nursing. I’m also a psychiatric nurse practitioner, and I practiced with the Nurse Practitioner Group at Columbia as well as in New Jersey. 


My role with Project AFFIRM has been from the beginning of the project, when I was a PhD student. I started in 2013, and I’ve been working with Walter since then. There have been a number of substudies and I’ve led two of the substudies. 

The first one was about nonsuicidal self-injury among transgender people, and then the second one, more recently, was among Latinx transgender people looking at discrimination, stress, and sleep. We collected various types of data, which was the first time we’ve done that with this cohort. We collected actigraphy data, which means monitoring sleep and wake patterns and activity levels. We collected two samples of saliva, one for cytokines, one for DNA, and we also did some blood pressure monitoring for feasibility to see if that would be something we might want to expand in future studies. In terms of the COVID-19 study, I’ve worked on formulating the survey, distributing the survey, and planning data analysis.


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You all come from various different backgrounds. Could you talk about your personal and professional paths to the work you’re doing now?

JEREMY KIDD: I came to Columbia in 2013. I’m actually back in rural Virginia now, where I grew up, waiting on my COVID test results so I can see my family! I went to medical school in Virginia, then came to Columbia in 2013 for psychiatry residency and was fortunate enough on my interview day to meet with Walter and I think at that point, AFFIRM was probably being planned, I don’t even know if it had started yet. 

But to come from a place where oftentimes I was trying to convince people to do LGBTQ health research, to scrape together resources to be able to do that, to come to a place and see this kind of research being really embraced was really eye opening and inspiring. I am also interested in substance use disorders and addiction treatment, and that’s also really well represented at Columbia. It’s been really great to get to bring my interests in both LGBTQ health and addiction treatment together and to work with the team here. 

For my personal path, the reason I got involved in a lot of the work is prior to medical school, I did a lot of community capacity building, working in the 
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community, a lot of advocacy and activism work, and I think those are the stories that I hold in my head and the relationships that I think inspired me to keep doing this work, because I recall all of the challenges and the discrimination and the things people that I really care about have experienced, even some people that I’m not in touch with anymore. Those are the stories and experiences behind the data that we’re looking at and the reason that I got involved in doing this work.


RENATO BARUCCO: My background is in psychology. I studied in Italy and moved to New York about 15 years ago. At the beginning, for about eight years, I worked in public health and in transgender healthcare services in underserved communities. I was working in South Bronx primarily, but also in Queens and Brooklyn, particularly with transgender women of color. We were providing mainly CDC (but not only CDC) approved interventions for sexual harm reduction, as they used to call it back then, but also making sure that all trans people in the community were connected to healthcare services that were competent and also affordable at the time, since many of them didn’t have insurance. Then, six years ago, I started working at Columbia, and since then, I’ve been focusing not only on transgender health but also on LGBT health as a whole, particularly LGBT aging.

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KASEY JACKMAN: I came to this work through the clinical route. I went to nursing school at Columbia, where I completed a bachelor’s in nursing and a master’s in psychiatric-mental health nursing. I practiced as a nurse practitioner for a while. ​
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 Then, I came back to do a PhD after seeing a lot of gaps in our understanding and in the evidence base for our clinical care, particularly among the patients I was working with, children and adolescents. 

In nursing, and in other healthcare fields too, there’s not much education on how to care for LGBTQ people, for example specific health needs, and even health disparities are not well known or understood among clinicians. In addition to my research, one of my other goals is to improve and augment the nursing education around caring for LGBTQ people. That’s a really important goal.


​WALTER BOCKTING: I’ve been working with transgender people since 1986 in research as well as clinically, as a psychologist. I came to Columbia after I served on the Institute of Medicine committee that took stock of what was happening across the country in terms of the health of LGBTQ people and the research informing the healthcare. When we did that assessment, we just recognized that a lot of the work had been on HIV and that there was a great need to go beyond HIV to also look at other health concerns that LGBTQ people have. 

I came to Columbia to help develop and implement a comprehensive research agenda.  Given that transgender people were my first love, so to speak, in terms of the work I’ve done all these years, we set out to develop a new study for transgender people, and we wanted it to be longitudinal so that we could actually get a sense of what the lives of transgender people were like over the life course. A lot of the work that had been done up to that point focused more on the time of transition, and we know that people’s lives go on after that, so that was the impetus for Project AFFIRM, the larger project in which we did this recent survey to find out how the people we are following are doing during COVID-19.




​How did you recruit people for Project AFFIRM?

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WALTER BOCKTING: We did it through something called venue-based recruitment. We have collaborators in San Francisco and in Atlanta, so in the three cities, we went out to various different venues, both online and offline, where trans and nonbinary people congregate, and we put the word out for our study, and people then signed up. They did that either in
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person or via our website, and from that, I think we had about 1500 people that registered for our study. From that, we chose a very diverse group, diverse in gender, diverse in age, diverse in race/ethnicity, for a total of almost 350 people in those three cities. Our goal was not to get as many people as possible; our goal was really to get a very diverse group that was recruited from the community and that we could follow over time. 

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JEREMY KIDD: One of the strengths of Project AFFIRM, as Walter was saying, is that it’s a cohort that’s been brought together and then maintained now for four years through a lot of engagement and research. The Project AFFIRM team, during more typical times, has also been out in the community and visible at community events. It makes it really easy to reach out to people in some ways because these are folks that all of us have, to a greater or lesser extent, gotten to know over the years. 

For the recent online survey, we reached out by email first to anyone who had been involved with the Project AFFIRM cohort over these past four years, which was relatively successful, although we realized that for a number of reasons, we needed to think outside the box in terms of reaching folks. Some people didn’t have access to email or had limited tech literacy and needed a different kind of approach. I also heard from at least one individual who had lost internet access as a result of losing financial support and access to employment during the pandemic, so we (I say we as though I did a lot of this work)—Renato and Theresa, another collaborator of ours, did the bulk of this work in terms of reaching out by phone to really try to make contact in any way that we could with these folks and, for the most part, administer the survey online. In some cases, the surveys were actually done over the phone with participants as well.
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What kinds of questions were asked in the survey and later in the in-depth interviews?


JEREMY KIDD: We focused the survey primarily on the impact of COVID-19 and measures that were taken or recommended by government officials to prevent the spread of COVID-19, so things like physical distancing, social distancing, and the uptake of those things among trans folks in ways that would be expected of anybody in the population, but also in some particular ways. We used a measure called the Pandemic Stress Index, which was developed at the University of Miami, to ask about some of the general ways that people’s lives had changed, in terms of cancelled travel plans, time spent at home, caring for sick loved ones, loss of employment, changes in housing status. 

We also asked about things that were more particular for this population, such as the loss of access to supports like LGBTQ-specific social supports or trans-specific social supports, community center groups, community organizations that people might have been a part of before but couldn’t access. 

The other area that we wanted to be sure to ask about were disruptions in gender-affirming care, so whether people had had gender-affirming surgeries that were either cancelled or postponed—I clinically hear from a lot of people who had a lot of difficulty, at various times, attaining gender-affirming hormone treatment, so disruptions in that—as well as disruptions in mental healthcare. We asked about those kinds of things as well. 

We asked about some other things that we thought might be affected, such as mental health, tobacco/alcohol/substance use outcomes, and sleep to cover other health outcomes that might have been impacted by some of the things that are happening in folks’ lives during the pandemic.

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WALTER BOCKTING: One of the nice things about doing this in an ongoing group that we’re following is that yes, we’re asking specific questions that are unique to this period of time, but we’re also able to ask them again how they’re doing in terms of their mental health, in terms of substance use, in terms of their wellbeing, so that we can actually see where they changed from previous years. 
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In terms of the in-depth interviews, that is actually something that we want to do. We have done interviews on other topics over the years, but given the response that we got to the open-ended questions in the survey, we really would like, going forward, to do the interviews because we realized that people really want to tell us their stories, which I think are very rich. Maybe this is a moment for you, Renato, to tell us a little bit of what you’ve gleaned from the analysis of those open-ended questions so far.

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RENATO BARUCCO: I just started working on this analysis last week, so this is just my impression. We’re still collecting the data and we’re also analyzing in detail what the participants said, but the first impression is that there are a lot of issues, and they are separated into two main categories. 

One is issues that probably a lot of people are dealing with or dealt with during the months of the pandemic in New York, with isolation and the feeling of being trapped in their apartment and not being able to go outside or to see loved ones or family, and also some changes in their lives: losing jobs, not being able to start a job, or not being able to pursue the plans that they had planned in the months prior to the pandemic. But these are issues that we can expect to find also in the general population. 

There is another set of issues that are specific for transgender and nonbinary people, and they came up in these answers. As Jeremy mentioned, a lot of people struggle with their inability to get in touch with other members of the community. A lot of people mentioned, “I wasn’t able to go to the group I used to go to,” “I wasn’t able to go to the gym with a friend of mine who happens to be trans, and we used to connect that way,” “I wasn’t able to go to a bar I go to,” or “I wasn’t able to meet with friends on game night,” because those moments were not just moments in which they socialized, but those were also moments in which they supported each other in some of the struggles that people who are transitioning or who transitioned experience. 
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Within these answers, I see a lot of solitude built upon a very hostile world. You have a hostile environment around you, and you have this community that really helps you negotiate and face some of the struggles, and then all of a sudden you don’t even have that anymore. So that was something that seems to be unique. I see a lot of people saying, “I really miss seeing my friends, and I really miss seeing people I used to go to the park with,” and a lot of people connect with the same people online, but it’s just not the same thing. 

Another aspect that can come in is disruption in living arrangement, because people couldn’t afford the rent anymore, so one of the roommates left, and now they have an empty room in their apartment and they don’t know who to let into the apartment, because you have to ensure your roommate is understanding, is supportive [of your trans or nonbinary identity]. A lot of people who break up right before or during the pandemic from their significant other also lose an important source of support. The two main things that we’re really noticing so far is the loss of the support system of the community, but also loss of their living arrangement, living situations in general. 

They also talked about not being able to access healthcare services as much as before. This was very important to some people, especially those who were about to go back on hormones or those who were starting some gender-affirming 
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procedures, medical procedures, because all of that was interrupted. But I have to say that most of these people said, “I was supposed to have surgery in 3 weeks, but all those sorts of medical procedures are now cancelled, so that’s frustrating, but I also understand that they need to do this, so ultimately I’m going to suck it up and it’s going to be okay for now.” 

That was the attitude, their understanding of the situation, while others really felt somewhat more endangered since they weren’t able to access the medical services because they didn’t have internet access or they didn’t know how to have a telehealth visit at the time. I guess that as the pandemic progressed, they probably found other strategies to see the doctors and probably were able to use telehealth. But that’s something that came up quite often as well: access to healthcare services, both in terms of physical healthcare, transgender healthcare specifically, and mental healthcare. 


WALTER BOCKTING: I think another way of saying what you said, Renato, is that our community, the community that we work with, relies a lot on each other for support, and the pandemic has affected that for many. The ways in which they connect are now suddenly not as easy to access. I think we see that a lot. They have their families of choice, their support in the community, and it has been hard to access that during this time. 

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KASEY JACKMAN: I agree that the loss of social support is really key. In our Latinx substudy, for example, people were not reporting very high levels of discrimination, but just the stress of living as a transgender or nonbinary person in a world that’s not set up for that, as one of our previous participants has expressed it, is very stressful, even if they’re not facing a lot of direct discrimination. I think the loss of that community support is very hard for a lot of people. 

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My other thought is about how we were talking about wanting to do more in-depth interviews with our participants. Again, we’ve done this in the past, and we’re planning to do it again with the COVID-19 study. I think that’s one of the strengths of Project AFFIRM, and something that’s kept people engaged with the study over the years. I’ve done some of the interviews at various stages, and some of the feedback we get is that participants appreciate the opportunity to tell their story, and that’s a phrase that’s commonly used. I think it’s important and powerful to give a voice to people who are often not heard or not listened to. 

​As a side note, I recently wore a Project AFFIRM T-shirt to the Queer Liberation March, and on the back, it says “tell your story.” That was our slogan when we started this study: tell your story. It’s a theme that has carried through this longitudinal study and all the substudies. I think it is really important for the community and has benefited our engagement with our participants, that opportunity for them to tell their story.

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JEREMY KIDD: And as I share with you some of the numbers, I think it’ll become clear why it will be so interesting and helpful to do these in-depth interviews because there are so many things behind some of these numbers. We did a survey near the end of March, shortly after the New York City stay at home order went into effect.  Atlanta had not, so you can imagine that it’s a bit of a moving target. We ran the survey until the end of June. 
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One of the challenges in describing what happens during a pandemic is that it continues to evolve. For instance, about 40% of the people that completed the survey had experienced at least one symptom of COVID-19, but at the time, what we were asking for were fever, cough, and shortness of breath, because initially that was all that the CDC was delineating as symptoms of COVID-19. Now, we know that there are other symptoms that have been added to that, including things like fatigue and new loss of sensations of smell or taste, but those were not part of the original definition of COVID-19 when we were starting this. 

But even though 39% of those individuals had experienced a symptom, only about 5.7% had received a PCR test, and only 1% had tested positive. Again, 
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if we think about the evolving nature of that, people who completed the survey in March or April wouldn’t have been able to get a test. People who completed the survey in June would have been able to get a test maybe, but even that has changed again as the pandemic has evolved. ​

About 70% of the cohort described the impact of the pandemic on their daily lives as extreme or very much in terms of the impact. There wasn’t a single person who said, not surprisingly, that their life wasn’t impacted at all by this. Almost all had been engaged in some sort of social distancing or isolation. 

This is a number that was very interesting to me: 30% of the cohort was unemployed at this time. However, only 16.7% of those individuals had lost their jobs during the pandemic. This sort of shows what a high unemployment rate there is among trans folks, and there’s lots of research out there describing why that probably is, and a lot of that is related to discrimination. If you look at the 30%, this is probably a comparable number to people that are losing their job in the general population, but about half of the people in Project AFFIRM had already had difficulty accessing employment even before the pandemic. 

56.7% reported some sort of personal financial loss during the pandemic, and about 30%, or almost a third of individuals reported difficulty accessing basic needs like food and medications during the pandemic. Over half reported loss of access to LGBTQ-specific supports, and about 40% reported loss of access to transgender/nonbinary specific support systems. 

11% had a surgery that was cancelled or postponed. About a third of individuals who are on hormones had experienced some sort of disruption in being able to access hormones. About half of our cohort was engaged in some sort of mental healthcare prior to the pandemic, and about a third of those individuals experienced some sort of disruption in their mental healthcare during the pandemic.

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This is just a first pass, but we’re going to begin looking at mental health during the pandemic. We’re going to be looking at substance use during the pandemic, and the advantage of the Project AFFIRM cohort is that we have similar information from people going back 3-4 years now, so we can look back and see how people’s mental health has changed over time, compared to when they sat down and participated in the interviews prior to the pandemic. 

But this, I think, shows in a numeric way some of the things Renato and Kasey were talking about and some of the things I think we’re hoping to learn in a much more granular way about what supports people were accessing before, what the ways are that they’re trying to augment that during the pandemic, 
what the ways are that those strategies are falling short, and how we as clinicians and public health researchers might be able to develop tools or interventions that could help provide more support, even in this current environment where we’re not all able to gather together in a room like we used to and hopefully will again soon.



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On the Project AFFIRM website, I noticed a particular theme being repeated: promoting resilience, developing resilience, among transgender and nonbinary individuals. I love that goal, because you’re not just finding something with your research, you’re building something and helping people grow. Could you talk about what that means to you?
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KASEY JACKMAN: I think often, transgender and nonbinary people are pathologized and when you hear the words transgender or nonbinary, you may think of news reports of people being murdered, frankly, or people who have mental health problems, or who are unstably housed or unemployed. 

There are many social determinants that are affecting the health of the community, but the flip side of that which isn’t as often spoken about is the resiliency and enormous strength in the community, living in a world that’s not understanding, for the most part, of who they are and their 
life experience. So the emphasis on resilience brings forth this other side: we need to understand the problems so we can help people to live fuller, healthier lives, but there’s a lot of existing strength in the community that we can further build on and develop.


WALTER BOCKTING: I’ll say that part of the reason for a longitudinal study is that we have already seen in our data that people learn and adapt over time. Yes, there continue to be challenges, and if anything, there has been a little bit of backlash. A lot of progress was made, certainly visibility, years ago, and the last couple of years have been a bit more challenging as some people have tried to undo some of the progress that was made. So we are seeing how people adapt to that and overall, I expect that the lives of trans and nonbinary people will continue to improve. Perhaps Renato can tell us about a specific example, I’m thinking about our employment study, on what we are doing to promote resilience.

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RENATO BARUCCO: The employment study is part of Project AFFIRM and we conducted a series of qualitative interviews with some of our participants to understand what some of the challenges were both while seeking employment as transgender or nonbinary people or transitioning while on the job: whether they required any sort of assistance from human resources or if it was something they dealt with by themselves. 

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In that research, in the past two years, we’ve analyzed the data, and what we’re trying to do right now is create a curriculum in collaboration with some corporations and with other not-for-profit organizations working with transgender communities to improve their access to employment, to improve their abilities to get employed, to transition while on the job. What we will do is come up with a training that will be available online for corporations that really want to diversify the workforce and include all of this talent that is out there, but for one reason or the other, they’re not recruited because of the barriers that are there for transgender people when accessing employment or being employed as they would like. 
For instance, a lot of them reported choosing to work for not-for-profit organizations or LGBT organizations so that they didn’t have to come out or have that conversation all together. But they desired, or they thought about, employment elsewhere. 

I also wanted to add, based on what Kasey said earlier, that even in these qualitative answers to the survey, very often you see gratitude toward these ongoing and longitudinal studies. A lot of the open-ended questions start with, “thank you so much for doing this job, a lot of things have changed since last year, but thank you for staying in touch.” I’m paraphrasing, of course. I just really wanted to highlight that because it comes back over and over again.


WALTER BOCKTING: I think part of our goal along the way is to have our information inform programs and policies to further promote resilience, improve conditions, and reduce barriers that people face. For employment, we’re going to work with companies and other employers to interest them and engage them into diversifying their workforce for greater inclusion of trans and nonbinary people.

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JEREMY KIDD: I neglected to mention that one of the other areas that’s included in our survey that we haven’t looked at yet is coping strategies that people utilize. I think that those will be really important to look at for all the reasons that everyone has been saying because that’s where we’re going to learn about the resilience that these individuals already have in their lives. 

Since these three sites were not impacted in the same way at the same time by the pandemic, it’ll be interesting to see what people are doing to cope with the stress and the isolation in different places, because that might provide insight into what we could think about offering and might be helpful to people in parts of the country that are now being more impacted by the pandemic so that they can learn from the resiliency that other people have been sharing with us.



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How has research on transgender and nonbinary health changed since you started, and where do you want to see it go in the near and far future?

RENATO BARUCCO: As I mentioned earlier, in the first part of my career, I wasn’t necessarily working on research, but we were working with the CDC, and they were doing the research with the data that we were providing them. What I noticed they needed was definitely more opportunities to participate in research and to participate in research that is specific about transgender health. Even ten years ago, all these interventions were about HIV/AIDS. They started realizing that it’s important that we better understand how to provide transgender healthcare, but that wasn’t the goal, necessarily. It became part of the goal, but they were interested in lowering the rate of HIV/AIDS infections and improving HIV care. 

While I see a lot more opportunities right now. Sometimes, and I don’t want to say too often, because that’s not the case, I feel like a lot of our participants get asked to participate in surveys and interviews by a lot of different entities. So I think it’s important to keep in touch with our cohort, to build that rapport, so that they know you and they feel more comfortable sharing their story, something that is not necessarily easy to do. It’s also important to compensate them for their time. It’s not just a matter of money, but recognizing that they are really giving you their story and their time to come in and talk to you and give you all this valuable information.
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KASEY JACKMAN: I agree with Renato. There’s been a mushrooming of transgender health research. I remember when Project AFFIRM started and we went into the field; there were two other large transgender health studies that went into the field the same year. There are increasing opportunities for our community to participate in these research studies, which I think a lot of them appreciate while some of them may feel over-researched or over-examined. 

One of the things that I think is better recognized now, is that the community really values having trans people involved in the research team. That’s something that comes up often among community members. Participants ask: “are there trans people in this research team?” or they give feedback such as “I appreciated recognizing someone on the research team who I could identify with.” Obviously, the trans population is a small minority, so it may be difficult, but I think that it’s something that researchers increasingly recognize is an important thing to do.

And finally, in response to the point about HIV research: even though a lot of trans health research started out as HIV research, some HIV research is still not inclusive of trans people. For example, some HIV research will include transgender women, but not transgender men. So we still see that as an under-studied group within HIV research.


WALTER BOCKTING: I will just say that what we talked about earlier, I think, is newer, that we are focusing more on a strength-based perspective. I think it is important to document all the challenges that people face, and we certainly will continue to do that, but it’s also now about resilience and the strengths, and how we can build upon those. I think that’s one of the shifts that I have seen over the years. 

I’m also thinking about your work, Kasey, that you alluded to earlier: using some emerging methods to look at biomarkers, so not only surveys and people’s self-reporting. As a psychologist, I feel that people’s own perspectives and how they are perceiving things, to me, are always the most important. But we have a fair amount of that which has been done. We’re moving into getting other measures, maybe, Kasey, you could say more about that.

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KASEY JACKMAN: That was something that was new for our cohort and quite novel for transgender health research in general, to gather different types of data from our research participants. As you were saying, Walter, traditionally, most of the data has been self-reported: we sit down, we interview people or administer a survey online to collect self-reported data, so these newer methods allow us to collect more objective data. 

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Sleep is very important since it affects so many chronic health conditions. Disturbance in sleep has the potential to play a role in the various health disparities we see in this population. Going beyond self-report data is something that hasn’t been done very often before in trans health research, certainly not with our cohort up to this point. So that’s taking the research in a different direction.

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JEREMY KIDD: I think related to that is this idea that research, whether we’re talking about depression, whether we’re talking about substance use, or whether we’re talking about trauma, has moved beyond self-report data. We’ve moved into the era of using MRIs, using biomarkers, using more sophisticated measurements. I think that for trans people, and really, this is a challenging thing for LGBTQ research across the board, our communities really deserve to have research done in the same cutting edge way as these other studies that have primarily cisgender, heterosexual folks, and frankly, mostly men, involved in a lot of clinical trials. 

I think it is really exciting to see some of the work Kasey’s doing using actigraphy, and I think thinking about how we can bring 21st century research methods to improve LGBTQ healthcare is really important. That includes intervention work, too, because I think that we have described health disparities in this population, but I think one of the opportunities that arises from Project AFFIRM is that we can actually do something about these disparities and really improve health for LGBTQ people in a more active way.
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Lastly, what gives you hope for the future? This can be related to your research, science in general, or society at large. Take it wherever you want!

RENATO BARUCCO: I think that what gives me hope mirrors what I’m learning from our participants, and that’s technology, which we know really comes with a lot of benefits, but it also comes with some concerns, especially regarding privacy and all of these different companies collecting information. Something that I noticed also from my experience during this pandemic and in the survey answers is that Zoom, Facebook, Instagram, and Reddit, as well as gaming platforms, like Discord, really became a lifeline to keep in touch with others. It’s still not the same, but everyone was mentioning, “I found this online group: it’s not my group or my friends, but at least I have that.”


JEREMY KIDD: I was really worried at the start of the pandemic, thinking about queer kids and queer youth, worrying about a lot of college kids who now had to live with their families again and what that was going to be like. But over the course of the pandemic, I bet every other week, I get a Facebook message or a text or an email, sometimes from somebody I don’t know that well, but often people who I’ve known in different phases of my life, who are saying, ‘“my kid just came out to me as queer or as trans or as gay, I want to know how to be supportive of them.” I don’t want to oversubscribe that to COVID, but parents are spending a lot more time with their kids, and kids are spending a lot more time with their parents and learning about them. I think that gives me such hope, to see parents in rural America, where there are not huge queer communities, reaching out and really proactively saying, “how can I be a better parent to my queer kid?” To see that happening in such a consistent, surprising way definitely gives me hope.


KASEY JACKMAN: I think the thing that gives me hope is the increasing attention and awareness to gender diversity and incorporating issues of gender diversity into curricula, whether it’s for healthcare providers in training or in schools and universities. Also, at the research level, we’ve had, among our team in the Program for the Study of LGBT health, success in obtaining NIH and private foundation funding for trans studies, which is really wonderful. Those things give me hope. 

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WALTER BOCKTING: I think for me, it’s the increased visibility of nonbinary identities within the community, and I think there’s also risk involved in that, we’ve learned that. For example, our people talk about how being engaged in advocacy is very important to them, but at the same time, that can take a toll on them. I think overall, it’s the increased visibility and the courage of people to stand up and share their experiences, share their story with us, including stories that are more diverse than the traditional narrative of transgender people. I think that really gives me hope, and I think it’s wonderful for the next generations, so that there will be a range of gender identities and expressions that they can relate to and find a sense of belonging with. 
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Interview Highlights: Providing Cardiac Care for Pregnant Women During COVID-19 With Jennifer Haythe

7/15/2020

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By: Hannah Lin (CC '23)
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Cover illustration: Vanessa Vasquez (SEAS '23)

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Jennifer Haythe, MD, is an Associate Professor of Medicine at the Center for Advanced Cardiac Care at New York Presbyterian Hospital-Columbia University Medical Center and the Division of Cardiology. 
​Follow Dr. Haythe on Twitter @DrJennHaythe!



The following is a heavily condensed version of the full interview. If you're interested, read more here.


Could you talk about the COVID-19 research that you’re involved in?
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I was involved with a group of cardiologists at the hospital led by Dr. Sahil Parikh which published an article in JACC about the cardiac manifestations of COVID early on. 

We are also awaiting acceptance on a paper about women and COVID, looking at what some of the socioeconomic impacts are for women getting COVID and the types of jobs they do, whether they really get COVID less or are just not getting diagnosed as much because they are less likely to come to the hospital. 
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​Finally, I do cardiac obstetrics, which is the care of pregnant women with heart disease, and the obstetrics group published a paper with guidelines on how to do telemedicine visits with pregnant women with different medical problems. I participated in the section on cardiac problems during pregnancy, how to manage during COVID, and what the recommendations would be for how to integrate televisits with in-person visits.


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How are you seeing pregnant women being uniquely affected by this pandemic?

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I think women have had a hard time in the labor and delivery world, especially initially, because the hospitals put restrictions on visitors, and I think there was about one week there when women who were pregnant were not allowed to have any visitors with them during delivery, which was incredibly difficult and emotionally taxing on these women. That actually ended up getting reversed, and they were allowed to have one visitor with them during the delivery. I think it’s been very stressful for pregnant women, since they’re having this beautiful thing happen to them, and they’re wearing a mask, their partner’s wearing a mask, everyone in the room is wearing masks and gowns, and it’s not exactly the warm and fuzzy delivery that people may have imagined for themselves. 


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You dedicated yourself to patients on the frontlines along with other healthcare providers during the peak of the pandemic in New York City. Could you talk about how you felt then and how you feel now, a few months after?

I think at the beginning, it was really very stressful. I have two children who are 12 and 15. We’re lucky enough that we have a family country house upstate, so my husband took them there, but then that meant that we were apart for chunks of time, which was hard. 

The beginning was really hard. I think it took a big emotional toll on many of us and I think there was a huge amount of fear because we hadn’t dealt with it before. What we were seeing was really at the level of chaos and war. It felt like a situation that no one had ever seen. 

I was actually incredibly overwhelmed in a positive way by my colleagues and how hard everybody worked, how devoted everyone was, how much they looked out for one 
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another, took care of each other, making sure that they were okay, they were safe. I felt the hospital handled it incredibly well from an organizational perspective, being very transparent, providing a lot of information. ​

I think for me personally, it was pretty hard in the beginning, having to travel to see my family, the unknown, the anxiety. I did feel like I had a lot of insomnia. It’s funny you asked because just, I would say, the last week or two, I’ve been starting to feel much more back to myself. I’m not wearing scrubs anymore, I’m wearing normal clothes, and I don’t have to wear Crocs! That’s been a lot better. 

But it was a good three months that were very challenging. We saw some of our colleagues become very sick and thought some of them would die, we know some people who died, and I think that was emotional for everybody.


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Lastly, what gives you hope for the future of cardiology, medicine, and society as shaped by everything that has happened this year (the pandemic, the fight for anti-racism)?

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From a medicine perspective, I feel very hopeful because I think in the next 10-20 years we’re going to see a huge change in how cancer’s treated, how heart disease is treated, how for so many illnesses, even neurologic diseases, genetic therapies and targeted therapies are going to make a huge difference for the treatment of people and hopefully become less and less invasive. 

From a societal perspective, I feel like despite how stressful and chaotic everything in the world is right now and sometimes people feel 
hopeless, I’ve seen so much goodness in people during this outbreak in the hospital, whether it’s nurses, doctors, travel nurses from the South who came up to work with the sickest of the sick COVID patients with a smile on their face and FaceTimed the families. ​​

I just always remind myself that there are so many people that are inherently good and that we’re bombarded with all this social media showing how terrible people can be. If you try to push through all that and focus on what you see around you, you’ll see that so many people deep down are incredibly kind, brave, and inspiring. 

The third, in terms of social justice, I think that in medicine, this has become an incredibly important thing to focus on, not only in providing equitable healthcare to all different kinds of minorities, which is a big focus for me in terms of cardiac obstetrics, knowing that the maternal mortality rate in this country is incredibly high, particularly among Black women, but across all areas of medicine. I think, at Columbia, they are making every effort, as they should, to make all minorities feel like they have no barriers, that they are not being discriminated against, that we are all equal and the same, and are taking note of past decisions that were not acceptable and trying to make changes as a result of that.
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Full Interview: Providing Cardiac Care for Pregnant Women During COVID-19 With Jennifer Haythe

7/15/2020

0 Comments

 
By: Hannah Lin (CC '23)

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Jennifer Haythe, MD, is an Associate Professor of Medicine at the Center for Advanced Cardiac Care at New York Presbyterian Hospital-Columbia University Medical Center and the Division of Cardiology.


Can you talk about your background in medicine and research and how you got into cardiology?


My path to cardiology was interesting. I really enjoyed cardiology as a resident, and at the time, there were only four cardiology fellows per year. You had to apply during your second year of residency as opposed to your third year, so you had to apply a year in advance of finishing residency. I wanted to start a family and felt like cardiology seemed very male-oriented and required frequent overnight calls. It didn’t seem like a lifestyle that was very appealing to me, so I actually initially matched in pulmonary critical care. 

I was in my gap year working in a clinic, and I ran into Donna Mancini, who was head of the heart failure transplant group at the time, in a garage elevator. She had been one of my attendings on the ward service when I was an intern and she asked me what I was doing. I explained to her what I had wanted to do and what I was doing, and she asked, “Well, why don’t you just drop pulmonary and come do a heart failure fellowship with me and work for me?” 

I thought about it and said I would do it. I did that for a year, and then I worked as a hospitalist for her for two years, and then she came to me and said, “I really think you should do a cardiology fellowship.” They were expanding the fellowship, so I was able to start as a general fellow the next year and then I went back to work in heart failure transplant after that.


That definitely is a very interesting path. Fast forwarding to now, could you talk about the COVID-19 research that you’re involved in?

I was involved with a group of cardiologists at the hospital led by Dr. Sahil Parikh which published an article in JACC about the cardiac manifestations of COVID early on, trying to draw attention to the fact that it wasn’t only ARDS that we were seeing but also plenty of cardiac manifestations like myocarditis, heart failure syndrome, stress cardiomyopathy, and arrhythmias. 

We are also awaiting acceptance on a paper about women and COVID, looking at why women seem to get COVID less, what some of the reasons are for that, what some of the socioeconomic impacts are for women getting COVID and the types of jobs they do, whether they really get COVID less or are just not getting diagnosed as much because they are less likely to come to the hospital. We were trying to tease some of that out.

Finally, I do cardiac obstetrics, which is the care of pregnant women with heart disease, and the obstetrics group published a paper with guidelines on how to do telemedicine visits with pregnant women with different medical problems. I participated in the section on cardiac problems during pregnancy, how to manage during COVID, and what the recommendations would be for how to integrate televisits with in-person visits.


I was just about to ask you about your work in obstetrics. How are you seeing pregnant women being uniquely affected by this pandemic?

I think that the division has done a really good job of trying to stay very connected with their pregnant patients and trying to do outpatient visits on pregnant women. There was a very interesting paper published in the NEJM about the COVID positivity rate in all women admitted for delivery, and they reported a pretty high incidence of asymptomatic COVID positivity in the community of women who were coming in, some of whom became symptomatic during their pregnancy, some of whom may have thought they were asymptomatic but were having symptoms of labor which may really have been symptoms of COVID. The positivity rate was 13.7%, which was high, and not expected, at the time, and provided insight to us about how much undiagnosed COVID was in the community. 

I think women have had a hard time in the labor and delivery world, especially initially, because the hospitals put restrictions on visitors, and I think there was about one week there when women who were pregnant were not allowed to have any visitors with them during delivery, which was incredibly difficult and emotionally taxing on these women. That actually ended up getting reversed, and they were allowed to have one visitor with them during the delivery. I think it’s been very stressful for pregnant women, since they’re having this beautiful thing happen to them, and they’re wearing a mask, their partner’s wearing a mask, everyone in the room is wearing masks and gowns, and it’s not exactly the warm and fuzzy delivery that people may have imagined for themselves. 

In terms of illness, we haven’t had any deaths in pregnant women from COVID. We’ve had women get sick after delivery and need medical care for COVID, and I actually couldn’t tell you right now what the transmission to the fetus is in our institution, I believe it’s either zero or very low.


Going back to the televisits, you wrote an op-ed in The Wall Street Journal titled, “House Calls are Back—Virtually.” Unfortunately, I don’t have a subscription, but I could read the first paragraph, where you talked about how virtual visits give you surprising insights into your patients’ health. What do you think the future of telemedicine looks like specifically for your specialty, cardiology? 

I think telemedicine is an incredibly useful tool, and I know that there’s been a lot of pushback, especially from community physicians who see a large volume of outpatients. I think that billing is obviously an issue for people trying to run a business in medicine. But there were a lot of rapid changes made that allowed for telemedicine to take off that I don’t think could have happened without COVID in terms of regulatory requirements and crossing state lines, having the ability to see people in different states where you’re not licensed but still allowed to do televisits with them. 

I think telemedicine is amazing. I know that there is always going to be resistance to new things, but I think it really fills a void especially for people of lower socioeconomic status, assuming that they have access to some kind of a smart device, people who are very disabled and for whom it’s very hard to get to the hospital, people who aren’t feeling great that day and can still be seen, people during COVID who were nervous to come to the hospital or who needed to minimize their exposure.

I also hope, in the future, that people will be able to consult with specialists that aren’t near their home and get ideas and recommendations that don’t require a huge cost to the patient to travel and see that specialist. I like to give the example that someone has a rare brain tumor, lives in a rural part of the country, and doesn’t have the resources to just take a trip to Chicago, New York, or some major medical center. They can have a visit with a neurosurgeon that specializes in that kind of tumor and a specialty board, and those specialists can review the images with the family and make a recommendation that can help them decide what they want to do. I think that telemedicine is going to make it much easier for people to get those kinds of consultations. I think that it’s going to be here to stay. 

I think that people are going to fill in the gaps in between regular visits in order to keep better tabs on people’s health, especially heart failure. For me, it’s great, because we can have a video visit where you can tell me what your weight is, you can show me if your legs look more swollen, I can see if you look short of breath, I can adjust medications, or I can say you need to come into the hospital. 

Obviously, procedure-based professions are going to be a little more challenging. You have to be here to get a procedure, but you could have all the workup done when the proceduralist does a televisit with you and then you can schedule the procedure right after. So it’s not totally useless for proceduralists, but there are specialties where it would be a bit more difficult. Dermatology might be hard; sometimes, you really can’t see as well on these video visits as in other types of things. Obstetrics, you need to examine the patient and see how far along the baby is, what’s going on, and they need to get ultrasounds. So there are areas where it’s more challenging, but for my group, it’s great.


Shifting away a bit, it’s been about three months since the peak of the pandemic in NYC. You dedicated yourself to patients on the frontlines along with other healthcare providers, away from your family, and a lot of providers have spoken out about the huge physical and mental burden they felt and still feel. If you’re comfortable talking about it, I thought I could give you some space to talk about how you felt then and how you feel now, a few months after.

I think at the beginning, it was really very stressful. I have two children who are 12 and 15. We’re lucky enough that we have a family country house upstate, so my husband took them there, but then that meant that we were apart for chunks of time, which was hard. I think, especially for my younger child, there was a lot of anxiety around my health and wellbeing, whether it was safe to come home and see them, and whether I could reenter the home safely. 

The beginning was really hard. I think it took a big emotional toll on many of us and I think there was a huge amount of fear because we hadn’t dealt with it before. What we were seeing was really at the level of chaos and war. It felt like a situation that no one had ever seen. Practically the whole hospital was COVID, every ICU bed was COVID except for one unit, popup ICUs were all over the hospitals, some had to have two patients to a room, some operating rooms had four patients to a room. 

I was actually incredibly overwhelmed in a positive way by my colleagues and how hard everybody worked, how devoted everyone was, how much they looked out for one another, took care of each other, making sure that they were okay, they were safe. Pretty much every surgeon in the whole hospital wasn’t doing surgery, and they formed a group to go out and put in lines in all the patients so that people didn’t have to fumble around with putting in lines in someone with overwhelming COVID. That was amazing. I felt the hospital handled it incredibly well from an organizational perspective, being very transparent, providing a lot of information. Dr. Craig Smith wrote these daily missives about the experience which were very uplifting. 

I think for me personally, it was pretty hard in the beginning, having to travel to see my family, the unknown, the anxiety. I did feel like I had a lot of insomnia. It’s funny you asked because just, I would say, the last week or two, I’ve been starting to feel much more back to myself. I feel safe in the hospital. Obviously, the numbers of patients have dramatically reduced, we have a lot of data to show that PPE works really well and there was very low transmission to healthcare providers once we started using PPE, and I’ve been starting to see patients in the clinic again, so even today felt like a normal day. I’m not wearing scrubs anymore, I’m wearing normal clothes, and I don’t have to wear Crocs! That’s been a lot better. I can sleep again. 

But it was a good three months that were very challenging. We saw some of our colleagues become very sick and thought some of them would die, we know some people who died, and I think that was emotional for everybody.


Thank you so much for sharing that. For students interested in going into medicine and specifically cardiology, do you have any advice or life lessons that you would like to impart?

I would say that medicine is a great profession, no matter what everybody else says. One thing I didn’t mention earlier was the toll that it took, seeing all these patients in the hospital who didn’t have their family members with them when they were dying or were very sick. The emotional support having to come from nurses and doctors there to try to help them communicate with family was very distressing but also showed how important our job is and really reminds everybody that medicine is a calling and that when things get crazy, your job is still really important. You don’t sit home and conduct business as usual over the internet, you really are in the trenches taking care of sick people. 

I think that cardiology is a great field. I wish more women would go into cardiology. You don’t have to do any procedures to be in cardiology, like me. If you want to do procedures, there’s plenty of them. The thing about medicine now is that there are so many different ways to practice it. You can be a cardiologist who only does echo, you can be an interventionist, you can be a general cardiologist, you can be an EP specialist. The same goes for all specialties. You can get as specialized or as general as you want, you can carve out the lifestyle you want in terms of how much you work. 

I’ve always thought medicine is a great career for women. The one area that is not as great is that we need to see more women being promoted and in positions of power. That goes for the entire country. 

I think people should know that it’s normal to doubt whether medicine was the right choice when you’re in medical school and residency. I think a lot of people ask what they’re doing there, why they did this, they feel tired, they feel useless, they feel stupid, they feel like they made the wrong choice and wasted all this time and money. But I think that if you can just keep going and find some people to talk to, you’ll realize that when you get to the other side, you’ll feel really lucky to have this job. I feel really lucky to have made this choice.


Lastly, to end with some optimism: what gives you hope for the future of cardiology, medicine, and society as shaped by everything that has happened this year (the pandemic, the fight for anti-racism)?

From a medicine perspective, I feel very hopeful because I think we’re really on the cutting edge of a whole new way of practicing medicine in terms of drug design and targeted therapies. For diseases that were very hard to treat, I think in the next 10-20 years we’re going to see a huge change in how cancer’s treated, how heart disease is treated, how for so many illnesses, even neurologic diseases, genetic therapies and targeted therapies are going to make a huge difference for the treatment of people and hopefully become less and less invasive, which we can see in cardiology with the advent of TAVR. There are very few reasons to have a surgical aortic valve replacement at this time, and eventually, that’s going to be true for so many other surgeries. That’s one.

From a societal perspective, I feel like despite how stressful and chaotic everything in the world is right now and sometimes people feel hopeless, I’ve seen so much goodness in people during this outbreak in the hospital, whether it’s nurses, doctors, travel nurses from the South who came up to work with the sickest of the sick COVID patients with a smile on their face and FaceTimed the families. I just always remind myself that there are so many people that are inherently good and that we’re bombarded with all this social media showing how terrible people can be. If you try to push through all that and focus on what you see around you, you’ll see that so many people deep down are incredibly kind, brave, and inspiring. That’s the second.

The third, in terms of social justice, I think that in medicine, this has become an incredibly important thing to focus on, not only in providing equitable healthcare to all different kinds of minorities, which is a big focus for me in terms of cardiac obstetrics, knowing that the maternal mortality rate in this country is incredibly high, particularly among Black women, but across all areas of medicine. I think, at Columbia, they are making every effort, as they should, to make all minorities feel like they have no barriers, that they are not being discriminated against, that we are all equal and the same, and are taking note of past decisions that were not acceptable and trying to make changes as a result of that.
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Full Interview: Tracking Transportation in New York City During the Pandemic with Juan Francisco Saldarriaga

7/8/2020

0 Comments

 
By: Hannah Lin (CC '23)

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Juan Francisco Saldarriaga, MS, MArch, is the Senior Data and Design Researcher at the Brown Institute for Media Innovation at the Columbia University School of Journalism. 


Can you talk a bit about your background and where you work?


I have degrees in architecture and urban planning from Columbia, and I also have a B.A. in philosophy. I am currently the Senior Data and Design Researcher at the Brown Institute. We are a bicoastal organization, both at the journalism school at Columbia and the engineering school at Stanford. We were funded by a gift by Helen Gurley Brown, who was the longtime editor of Cosmopolitan magazine. We try to combine technology and tools with reporting and storytelling. Every year, we give around 1 million dollars in grants to different teams that are doing interesting things combining tools, technology, storytelling, and journalism.  



You research at the intersection of so many different fields. Those are, and I’m quoting directly from your website, data, geographic information systems (GIS), visualization, journalism, architecture, urbanism, and the humanities. How did you get into this work? 

I first got into GIS, geographic information systems, and mapping in my urban planning masters. When I graduated from that, I started working in the Spatial Information Design Lab, which was a lab at the architecture school at the time. There, we were doing research on data visualization, working specifically with datasets around cities and transportation: urban data. Then, the Spatial Information Design Lab became what’s now the Center for Spatial Research after we received a big grant. I was one of the main researchers there. 

Part of what made the Spatial Information Design Lab special was that we often collaborated with people from other disciplines. That included the Brown Institute for Media Innovation, where I work now, because a lot of the ways in which we were trying to present information and data overlapped with the work that journalists do in telling stories. 

We also collaborated a lot with people in the humanities because a lot of the datasets we work with around cities, population, and migration are also humanities datasets. There are also travel diaries. There are also letters between people who are corresponding from one city to another. There are also datasets about forced migration. For us, it was crucial to not only get different perspectives in terms of how we were telling the stories but also in terms of the actual topics, so we needed to collaborate with experts in the field.



Can you describe the research you’ve been doing related to the pandemic?

We’ve been doing two things. One is a more general Brown Institute initiative. In early March we decided to do a rapid call for proposals around COVID and journalism or research. We put out the request for proposals and set a deadline of ten days for submission and evaluation. We had a very fast turnaround; we wanted to give our response back in three or four days. 

These were for microgrants, so we were giving out around 5000 dollars. We had quite a small budget, around 25,000 dollars, but we had an enormous response. We had more than 300 proposals combining journalism, storytelling, and data visualization around COVID—proposals from local newsrooms, from developers, from NGOs, from community organizations. 

There was a very interesting proposal that wanted to study domestic violence during COVID, because the hypothesis was that we would see much more domestic violence. There was another one that wanted to include machine learning in how they process questions from the audience for a radio station so that the responses could be more efficient and automated, freeing up time for journalists. There was another very interesting one from a radio station in Alaska, where they wanted to just get equipment so that they could transmit their COVID-related information better to a broader audience—it was the only radio station that covered a big swath of land, and without that, the community didn’t have any information. Our teams got together for a week and read all the proposals. We were happy to give out the grants, which have already started producing good results. 

On a more personal level, I am currently doing a research project around transportation and COVID in New York City in partnership with David King, who is a researcher at Arizona State University. We are looking at how the choice of transportation mode for New Yorkers has shifted throughout the crisis. Initially, we wanted to test whether there had been a similar decrease in usage of all transportation modes, especially subway and Citi Bike. Our hypothesis was that people actually switched to Citi Bike for a little while before everything shut down, so we wanted to compare the decrease in both transportation modes. 

We’re still working on it, so we haven’t published it or written it, but what we found was that both transportation modes decreased simultaneously in a very parallel manner, in a similar magnitude of decrease. They didn’t decrease from one day to the next; it took them over 8-10 days to really shut down, but for both of them, if you see the curve, they really mirrored each other.

What’s been interesting has been the reopening. We have actually seen that the number of riders taking the subway has really not picked up that much, whereas the number of people riding Citi Bikes and moving around on bicycles—the city has bicycle counters on the bridges—has picked up. Right now, we’re in the middle of testing whether they have picked up to normal levels, or whether they’re still below normal levels. That’s one step we still have to figure out. 

We also still need to figure out what kinds of trips these are, because these could be trips of people going to work that have replaced subway trips, or these could be different kinds of trips: a person locked at home who decides to go for a ride after lunch, a person who decides to bike to the supermarket. We want to understand what kinds of trips are the ones that have picked up, if it’s a substantially different kind of trip or if it’s a commuting trip and people are actually replacing subway trips with bike rides. 

Finally, the other thing we want to understand is the spatial distribution of these changes. There have been a few good analyses looking at the decrease in subway usage and how the decrease, even though it was enormous (more than 50%), has not been uniform across the city. Some neighborhoods have seen decreases around 90%, while others have seen decreases around 40%. That’s pretty much tied to demographics, especially income and people who are deemed essential who are, most of the time, in lower-income neighborhoods that are still relying on public transportation. We want to understand what the spatial distribution of that decrease is and what the spatial distribution of this new rise in Citi Bike usage is. Citi Bikes, of course, don’t cover the whole city, so how does that play out compared to the subway?



How exactly do you go about getting the data, especially if you’re trying to distinguish the commute type, between going to work or the supermarket?

All of these datasets are publicly available. For subway data, you can get it by station and you can get the number of entries and exits per station, but you can’t really tell the type of trip. You can tell that a person entered in one station and that another person (or the same person, who knows) exited in another station. 

Citi Bike does make their detailed data available, so that means you can see each individual trip. You cannot track users across the system, but you can see that this trip started in this station and ended in that station. In the case of Citi Bikes, you can tell the duration of the trip, the time of day, and the origin and destination neighborhoods, and you can infer whether those are commuting trips or not by the time of day in which they happen and their origin and destination—whether it’s a residential neighborhood as an origin or an office neighborhood as a destination.

For bicycle counters, you can’t tell what type of trip it is, but by the location of the counters, you can infer some things. Let’s say you see a lot of Citi Bike activity in Brooklyn but you don’t see that much activity on the bridges, where the counters are. You could infer that there are a lot of people biking, but not necessarily biking to work. All three datasets are public and available and are updated on a fairly regular basis, but they’re not exactly the same in terms of the amount of detail they give.



Will this transportation research project be going on for the foreseeable future?

I want to get it out soon. This is the thing with academic projects—they always take way, way longer than you want. Ideally, it will go out to an academic journal and, at the same time, to a news outlet, just because I am in the journalism school. We still have to write it up and see if our conclusions are interesting and novel and worth publishing. Hopefully, they will be, but you never know.



What projects are you looking into for the coming future?

There are a few research projects that I have in the back of my head. There is one urban planning project looking at segregation in cities, especially in Colombia, the country where I’m from. Cities there are divided by income levels. There’s a map that actually says, “this neighborhood is middle income, this neighborhood is low income,” and depending on that designation on the map, you pay different rates for your utilities and different taxes for your property. It’s a sort of government-sanctioned economic segregation. I’ve been collecting Twitter data on how people talk about the segregation for around two or three years, and I want to do an analysis where I test how much this policy has influenced the way people talk about segregation.

There are other things we do at the Brown Institute. As I said, we give out a million dollars in grants. In this year’s cohort, a lot of grants have to do with COVID or with the protests around the killing of George Floyd. One of my main jobs is to accompany these grants and help them throughout the year. We have a grant that is looking back at the 1994 crime bill and the Central Park Five case and looking at how the media was talking about crime in that moment to understand the role it played in racializing crime. That’s one of our biggest grants, with a team from Columbia and Stanford, so a bicoastal grant, which we really like. 

There are a couple more. There is a very interesting one going on right now, in which we are helping a researcher submit FOIA requests to local or state agencies around COVID, so requesting those agencies to give us everything they have that mentions COVID. My boss says that we’re writing the first draft of history by seeing how city and state administrators are dealing with COVID. The researchers in the grant have uncovered very interesting ways in which different cities have approached the pandemic.

For example, there was an article in The New York Times about a month and half ago about how New Orleans was preparing for COVID, especially around Mardi Gras, and the way they were able to tell that was from the emails that we got. There was another series of articles around meatpacking plants in Kansas and how the state officials knew that the plants were big hotspots, but they kept that from the public. That’s a very interesting project around COVID that’s happening right now on which I am working as an advisor, helping the grant group.



What is your perspective on how the pandemic is shaping the future of journalism and data?

From what I understand, journalism is in a very important moment. Before the pandemic, it was in a difficult financial position. However, with the pandemic, with all the other things going on, the value of journalism is becoming more clear and people are starting to realize that supporting good journalism is important not only for themselves but also for a healthy democracy. I’m hoping that that really serves to maintain the good journalism that is happening and to encourage more of it. 

I think journalists are becoming very good at working with data and at questioning data. Data is an incredibly powerful resource, but it’s also something that needs to be questioned and well understood. You shouldn’t put all of your trust in a dataset. Journalists are becoming very good at doing that, so I am hopeful. I see a lot of experimentation happening in news outlets, a lot of experimentation in visualization, which is great. I would say they are leading the way in experimenting around visualization, and that’s something that everyone is benefitting from. I’m very happy to be in this area at this moment, because I think it’s very exciting. 



For students who want to head toward a similar career path that you’re on, do you have any advice or life lessons that you want to impart?

I often wish I had studied computer science and had more of a background in the more technical aspects of my work. That would make it much easier. At the same time, I value my training in urban planning, architecture, and philosophy for giving me the conceptual foundations and a critical eye, both in terms of design and also conceptually in how to understand problems. I see a lot of analysis done just because someone knows how to use a tool, but they haven’t really thought about what it means or what kind of analysis is the appropriate one. 

I would encourage trying to get both, if possible. The technical aspect is something that can be learned on your own, which I did, so that’s possible and that’s great, but a more rigorous technical training would be better. A rigorous training on a subject matter, like urban planning, architecture, or the humanities, is also very valuable. So, hopefully, get both!
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Interview Highlights: Tracking Transportation in New York City During the Pandemic with Juan Francisco Saldarriaga

7/8/2020

0 Comments

 
By: Hannah Lin (CC '23)

Picture
Cover illustration by: Arooba Ahmed (CC '23)

Picture
 Juan Francisco Saldarriaga, MS, MArch, is the Senior Data and Design Researcher at the Brown Institute for Media Innovation at the Columbia University School of Journalism.


The following is a heavily condensed version of the full interview. If you're interested, read more here.


You research at the intersection of so many different fields. Those are, and I’m quoting directly from your website, data, geographic information systems (GIS), visualization, journalism, architecture, urbanism, and the humanities. How did you get into this work? 


I first got into GIS (geographic information systems) and mapping in my urban planning masters. When I graduated from that, I started working in the Spatial Information Design Lab, which was a lab at the architecture school at the time. There, we were doing research on data visualization, working specifically with datasets around cities and transportation: urban data. ​

Part of what made the Spatial Information Design Lab special was that we often collaborated with people from 
Picture
other disciplines. That included the Brown Institute for Media Innovation, where I work now, because a lot of the ways in which we were trying to present information and data overlapped with the work that journalists do in telling stories. We also collaborated a lot with people in the humanities because a lot of the datasets we work with around cities, population, and migration are also humanities datasets. ​



Can you describe the research you’ve been doing related to the pandemic?

Picture
We’ve been doing two things. One is a more general Brown Institute initiative. In early March we decided to do a rapid call for proposals around COVID and journalism or research. We had more than 300 proposals combining journalism, storytelling, and data visualization around COVID. 

There was a very interesting proposal that wanted to study domestic violence during COVID. There was another very interesting one from a radio station in Alaska, where they wanted to just get equipment so that they could transmit their COVID-related information better to a broader audience—it was the only radio station that covered a big swath of land, and without that, the community didn’t have any information. 
​

On a more personal level, I am currently doing a research project around transportation and COVID in New York City in partnership with David King, who is a researcher at Arizona State University. We are looking at how the choice of transportation mode for New Yorkers has shifted throughout the crisis. Initially, we wanted to test whether there had been a similar decrease in usage of all transportation modes, especially subway and Citi Bike. Our hypothesis was that people actually switched to Citi Bike for a little while before everything shut down, so we wanted to compare the decrease in both transportation modes. 
Picture
We’re still working on it, so we haven’t published it or written it, but what we found was that both transportation modes decreased simultaneously in a very parallel manner, in a similar magnitude of decrease. 

What’s been interesting has been the reopening. We have actually seen that the number of riders taking the subway has really not picked up that much, whereas the number of people riding Citi Bikes and moving around on bicycles—the city has bicycle counters on the bridges—has picked up. Right now, we’re in the middle of testing whether they have picked up to normal levels, or whether they’re still below normal levels. 
​​

Picture
We also still need to figure out what kinds of trips these are, because these could be trips of people going to work that have replaced subway trips, or these could be different kinds of trips: a person locked at home who decides to go for a ride after lunch, a person who decides to bike to the supermarket. 

Finally, the other thing we want to understand is the spatial distribution of these changes. There have been a few good analyses looking at the decrease in subway usage and how 
the decrease, even though it was enormous (more than 50%), has not been uniform across the city. Some neighborhoods have seen decreases around 90%, while others have seen decreases around 40%. That’s pretty much tied to demographics, especially income and people who are deemed essential who are, most of the time, in lower-income neighborhoods that are still relying on public transportation. ​



What projects are you looking into for the coming future?
​

There are a few research projects that I have in the back of my head. There is one urban planning project looking at segregation in cities, especially in Colombia, the country where I’m from. Cities there are divided by income levels. There’s a map that actually says, “this neighborhood is middle income, this neighborhood is low income,” and depending on that designation on the map, you pay different rates for your utilities and different taxes for your property. It’s a sort of government-sanctioned economic segregation. I’ve been collecting Twitter data on how people talk about 
Picture
the segregation for around two or three years, and I want to do an analysis where I test how much this policy has influenced the way people talk about segregation.

There are other things we do at the Brown Institute. In this year’s cohort, a lot of grants have to do with COVID or with the protests around the killing of George Floyd. One of my main jobs is to accompany these grants and help them throughout the year. We have a grant that is looking back at the 1994 crime bill and the Central Park Five case and looking at how the media was talking about crime in that moment to understand the role it played in racializing crime. That’s one of our biggest grants, with a team from Columbia and Stanford, so a bicoastal grant, which we really like. 



What is your perspective on how the pandemic is shaping the future of journalism and data?

From what I understand, journalism is in a very important moment. Before the pandemic, it was in a difficult financial position. However, with the pandemic, with all the other things going on, the value of journalism is becoming more clear and people are starting to realize that supporting good journalism is important not only for themselves but also for a healthy democracy. I’m hoping that that really serves to maintain the good journalism that is happening and to encourage more of it. 

I think journalists are becoming very good at working with data and at questioning data. Data is an incredibly powerful resource, but it’s also something that needs to be questioned and well understood. You shouldn’t put all of your trust in a dataset. Journalists are becoming very good at doing that, so I am hopeful. I’m very happy to be in this area at this moment, because I think it’s very exciting. 
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