Editor’s note: The opinions expressed by the author do not necessarily reflect the opinions of the AAMC or its members.
In January 2021, Kwame [not his real name] was diagnosed with COVID-19, just like many other people. Within a few days, his condition worsened significantly: His fever continued to rise, he experienced increasing shortness of breath, and his muscles ached persistently. With no relief in sight, he eventually sought medical attention at an emergency department (ED) in Oakland, California.
At the ED, medical personnel ran a variety of tests, including one that measured his blood oxygen saturation levels, a key metric for diagnosing the severity of a COVID-19 infection. The test used a pulse oximeter, a small device that clips onto your finger and measures how much oxygen your red blood cells are carrying. When his test results came back, doctors told Kwame that he was a fit, healthy young man and that he would recover just fine. They encouraged him to go home and rest.
But he refused.
A few weeks before, Kwame had seen a video on social media suggesting that pulse oximeters don’t always work well on darker skin tones. In between gasps for air, he tried to recount to the doctors what he had learned: Because of its increased melanin, darker skin absorbs more infrared light from pulse oximeters, causing Black patients to be three times as likely to have overestimated oxygen saturation levels.
Kwame’s doctors listened to his concerns and ended up admitting him to the hospital. It was good that they did. Before the end of the day, his condition worsened, and he was transferred to the intensive care unit. Fortunately, he was intubated and received the supplemental oxygen he needed to recover. Had it not been for a single social media post, however, his story most likely could have gone another way.
The video that Kwame serendipitously saw was one that I had made in December 2020. It was my first “Racial Bias in Medicine” TikTok video, which I created after reading a New England Journal of Medicine article about disparities in pulse oximeter readings. Since that video, I’ve been dubbed the “Medical Mythbuster” for creating more than 500 short-form educational videos that collectively have received over 140 million views, and I’ve built a community of 850,000+ medical students, educators, and patients across social media.
And the journey is just beginning.
Becoming the “Medical Mythbuster”
When I started attending Washington State University Elson S. Floyd College of Medicine in Spokane in 2019, the concept of race was already on my mind. I was part of my school’s third class, yet one other person and I were the only Black students out of 200. In a field where less than 6% of all physicians are Black, I wasn’t surprised. What’s more, I had already begun to think about what it meant to be one of the few Black men in medicine, and the legacy I hoped to leave behind.
The COVID-19 pandemic hit when I was halfway through my first year of medical school. In my classes, I kept hearing that Black, Indigenous, and other people of color were more susceptible to COVID-19. But professors often failed to include how a history of discrimination and the social determinants of health contributed to those disparities.
I was angry. Sad. Disheartened. Confused. But I knew I wanted to do something to effect change. So, I took to using TikTok and Instagram to educate audiences about systemic racism and the racial disparities that I had seen in medicine.
Then, my school’s curriculum went entirely virtual. During the first few months of isolation, I had a lot of time to myself. I remember reflecting on the murder of Ahmaud Arbery, a 25-year-old Black man who was fatally shot while jogging. He had been the same age I was. I remember watching the video of Chris Cooper, who was falsely accused of harassing a White woman in Central Park. And of course, I mourned the police murder of George Floyd.
I was angry. Sad. Disheartened. Confused. But I knew I wanted to do something to effect change. So, I took to using TikTok and Instagram to educate audiences about systemic racism and the racial disparities that I had seen in medicine.
My goal was to discuss health disparities in an easily digestible way, bust medical myths, and tell the untold stories of race in medicine.
Battling health inequities via social media
The video that Kwame saw became an instant success, receiving half a million views and thousands of comments in 24 hours. Not long after, I was invited to speak at the Food and Drug Administration about biases in health care that I had witnessed as a medical student.
In another video, I discussed the implications of using race-based algorithms to diagnose disease. For example, in the United States, an equation called the eGFR (estimated glomerular filtration rate) measures how well an individual’s kidneys are working. A low eGFR signals to physicians that your kidneys aren’t working properly, and it is used to determine whether a patient might benefit from dialysis or a kidney transplant.
For Black patients, however, a multiplier has systematically been added to the eGFR, raising that number and therefore making it less likely that physicians recommend certain treatments for them. One study estimated that without the adjustment for race, 3.3 million more Black Americans would have been diagnosed with a later stage of chronic kidney disease. And the reason the equation existed was a racist assumption that Black people have more muscle mass than people of other races. A new equation wasn’t created until 2021.
In my medical school dermatology unit, I rarely saw my own skin tone represented, so I created videos showing how dermatological conditions look on darker skin. Before I knew it, my inbox was flooded with people saying this was the first time they had seen their own dermatological condition represented on darker people. This disparity isn’t surprising, given that a 2020 analysis of medical school textbooks reported that the percentage of images of dark skin ranged from just 4% to 18%.
After viewing my video about a rare type of melanoma that is more common in people of African and Asian ancestry, acral lentiginous melanoma, a follower let me know that it caused them to get their own strange mole biopsied. The mole turned out to be precancerous, and they had it treated immediately.
Each of these and my other videos has received millions of views and thousands of comments.
It has been both humbling and empowering to know that my mission to unveil racial disparities is working well. It’s led me to serve as the youngest member of the White House Healthcare Leaders in Social Media Roundtable, work alongside the Surgeon General’s office on physician burnout and the youth mental health crisis, and speak on such prominent platforms as Good Morning America. I even received a personal message from Oprah!
But what has meant the most to me are the hundreds of stories I have heard from individuals who prove that when patients have access to clear, evidence-based research about how disparities can impact their health, it can bridge the gap between patient and provider and lead to better, more equitable care.
Succeeding on social
Social media has revolutionized how patients relate to their health, providing platforms for individuals to become informed, engaged, and empowered — and ultimately leading to better health outcomes.
Research shows that 1 in 10 patients get their health information online. That means physicians need to have a presence online as well.
And there’s no end to the type of content that providers can make. If you’re an OB/GYN, sharing the impact of access to prenatal care on birth-related inequities would be incredibly useful for both medical students and patients. If you’re an emergency medicine or primary care doctor, you could discuss the increased health risks that individuals who are unhoused face. Medical students can highlight health disparities that we notice as we progress through our medical school curricula.
Research shows that 1 in 10 patients get their health information online. That means physicians must have a presence online as well.
However, doctors often feel ill prepared to figure out what and how to post on social media.
One of the suggestions I offer physicians is to think about the most common questions they receive from patients every day. Did a patient ask you about the safety of vaccines? Or what a diagnosis of diabetes means for their daily life? Did you help a patient understand the long-term impacts of high blood pressure? The answer to each of these questions is a potential video that can educate a broader audience with accurate, evidence-based information.
When creating content on social media, it’s important to remember to avoid jargon. In medicine, we can suffer from the “curse of knowledge,” the tendency to assume that others have the same background information we have. Instead of saying “myocardial infarction,” call it a heart attack. Instead of “myalgia,” say muscle pain. Otherwise, you risk confusing members of your audience or making them feel excluded.
To succeed, it also takes an understanding of the social media landscape and the ever-elusive algorithms that determine what content makes it into users’ feeds. On TikTok, short-form video is the most popular, so if you prefer to talk in short sound bites and like showing visuals, then TikTok is a great platform for you. If you enjoy writing, Twitter rewards that, and is the perfect medium to begin briefly describing medical cases. Instagram pushes a mix of short videos and static images, providing an opportunity to demonstrate the day-to-day of your life in medicine in engaging ways. Any content you create can be repurposed, reused, and reposted repeatedly to reach new, broader audiences.
And while the future of many of these social media sites is uncertain (take, for example, the recent discussions of banning TikTok in the United States), what is sure not to change is that patients will continue getting their health care information online.
Health care providers need to step up and lead the conversations about medicine on social media. If we don’t, others will jump into the gap and may do so in ways that don’t serve patients. When we do, medical professionals can dispel inaccuracies, provide evidence-based information, and help patients better advocate for themselves.
As physicians we all have the power to be medical mythbusters and to mend the disparities in care that impact the most marginalized communities. Imagine how much we can accomplish collectively if more of us do this work. It just takes the courage to click “post.”