When Stacy Jones arrived at medical school at Harvard University, she was prepared to struggle. She’d always been aware in the back of her mind that certain aspects of academics were tough for her. She figured she’d just have to work even harder. But that “work harder” strategy didn’t work out so well.

“I basically almost failed a lot of my classes,” Jones said. “During that time I felt very ashamed and I felt very lonely.”

She avoided her professors, terrified they were thinking she was lazy. Then the summer after her first year, in 2015, Jones went to get evaluated. She realized she had a learning disability and attention deficit/hyperactivity disorder.

“It was very validating when my neuropsychologist sat down with me and said, ‘Stacy, you’re smart. Stacy, look at all of these things your brain does well. It must be so frustrating that when you read or listen to lectures your brain is not processing language in the same way,’” Jones said.

It was a relief to hear all that. But a concern, too.

“I think there is this perception in medical education, and in the culture in general, of not really admitting vulnerabilities,” Jones said. “’Disability’ isn’t a word that I often heard spoken.”

Disability hasn’t been talked about a lot within the profession. Doctors — the ones charged with treating everyone else — are often portrayed as pinnacles of health, super humans responding to emergencies around the clock. They’re the fixers, not the ones in need of care or accommodation.

Yet a growing movement of current and aspiring doctors says this narrative is a disservice. They’re trying to change the culture amid new research on disabilities in medicine.

Lisa Iezzoni, a professor of medicine at Harvard and director of the Longan Institute Health Policy Center at Massachusetts General Hospital, is very familiar with the culture of medicine.

“This profession historically has viewed themselves as able-bodied in the extreme,” Iezzoni said.

Iezzoni uses an electric wheelchair or scooter to get around. In the early 1980s, when she was in medical school herself at Harvard, Iezzoni was diagnosed with multiple sclerosis. She wasn’t in a wheelchair then, but she was experiencing some “shadowy” symptoms, like a loss of sensation in a limb. She wasn’t able to stay up late at night, due to fatigue.

She says her advisers knew this, and they treated her differently because of it. So did just about everyone else.

Iezzoni say one experience in particular stands out: She was scrubbing in on a surgery.

“The surgeon — at a slack time during the operation — turned to me and said, ‘Do you want my opinion about whether you should become a doctor?’ And what was I going to say? I’m a third-year medical student. I said, ‘Certainly, Dr. so and so. I would be happy to,’” she said. “And he then opined that I had no right to go into medicine because I lacked the most important quality in medicine. And that was 24/7 availability.”

Iezzoni says after that point, the residents overseeing her program ignored her.

“I was beneath their notice, because their attending [surgeon] told them I had no right to be in medicine,” she recalled.

Iezzoni didn’t become a doctor. She says she just didn’t have the support.

But she didn’t leave medicine.

“The work that I do is on disparities in health care for people with disabilities, and I think that part of the origins of disparities are stigmatizing attitudes,” she said.

Iezzoni says her medical school experience happened six years before the Americans with Disabilities Act passed in 1990. The landmark legislation created federal protections for people with disabilities.

In the decades since, amendments and court rulings have clarified those rights. But Iezzoni and others say those changes have been slow to take hold in medicine.

Research has found that, as future doctors advance through their training, they may become “more hardened,” says Iezzoni, and develop more negative views about people with disabilities. More recently, she has been interviewing doctors about their knowledge of disabilities for an upcoming report. She identified attitudes among some that gave her concern. Just about everyone said they’d never been trained about the ADA.

“They’d heard of it but had no formal training in what that meant about their responsibilities toward patients with a disability, what their responsibility is to care for people with a disability,” she said.

Earlier this year, Meeks had a thought: If doctors with disabilities saw more people like themselves, would they talk more openly about the challenges and opportunities? She started the hashtag #docswithdisabilities. The goal was to find 20 doctors willing to share their stories.

“There’s no end in sight,” Meeks said.

She has been flooded with interest from doctors with disabilities. (And now #nurseswithdisabilities have joined in, too).

That includes Nichole Taylor, an anesthesiologist at Wake Forest Medical School who has multiple sclerosis, and Erica Dwyer, an internal medicine resident at Cambridge Health in Boston.

“I was actually born deaf in one ear,” Dwyer said. “I was almost done with medical school, and then realized that I was also losing my hearing on the other side. And I started needing technology to sort of help amplify my hearing and to help manage in clinical settings and the like.”

Jason Brookman is an anesthesiologist in Baltimore who has attention deficit disorder. Brookman published a case study about himself about how he’s learned to managed his disability. It hasn’t always been easy, he says, and he only recently publicly identified himself as the person featured in the case report.

Another vocal participant is Feranmi Okanlami. He had a spinal cord injury and became partially paralyzed after a diving accident during his third year of medical residency in 2013. He returned to practicing and is at Michigan Medicine now.

He doesn’t want to be viewed as “an anomaly.”

“Once people see how many people are out there practicing with disabilities, I think that will normalize this more,” Okanlami said. “Disability does not mean inability.”

Okanlami might not be the guy on the ground doing the chest compressions during a code, when someone has stopped breathing, but he says a doctor is more than that.

“You have to be the person deciding what medication to give. You have to make sure that the people doing chest compressions are doing it adequately. You have to think about why the person stopped breathing, or their heart stopped,” he said. “The tasks required to run a code aren’t just physical tasks.”

Stacy Jones, who has completed three years of medical school at Harvard, says getting diagnosed with a learning disability after her first year and then later figuring out what she needed has made all the difference. One “gamechanger” has been using text-to-speech technology on her computer.

“It’s not just, you know, OK, I can read faster now,” she said. “It’s actually allowing me to take that burden off to actually learn.”

Jones says she struggled sorting out what to do after she was first diagnosed and figuring how and where to get support. Last year, she started connecting with other medical students and doctors with disabilities from around the country.

“We formed this national group — the national medical accessibility group called NMAC — out of this idea of de-stigmatizing disability in medicine, bringing peers from across the country, and Canada, too, for peer support,” Jones said.

So far that has included some 50 people — mostly medical students, but some nursing, pharmacy and occupational therapy, and others as well — from about 40 different schools. They’re advocating for better systems for people with disabilities in medicine, for more awareness across the field, and for support, especially for “some people whose voices have felt silence because of the structures and the systems as they are right now.”

These kinds of connections have made all the difference for those starting out, like Jessica Laird. She’s wrapping up year one of med school back at Harvard.

“To have that be the beginning of medical school and see students who were succeeding in older years who had disabilities was a really amazing way to start medical school, to know I wasn’t alone in this process,” said Laird, who was diagnosed with a rare connective-tissue disorder called Ehlers-Danlos syndrome in high school, and who recently got involved with disability awareness activities on campus. “The experience of being ill is so central to why I wanted to become a doctor.”

Meanwhile, since Jones began raising awareness about disabilities following her diagnosis, the medical school has been reviewing its policies. It’s now actively looking to hire a full-time disabilities-service provider, something that is identified as a best practice in the new AAMC report.

— (WHYY/The Pulse)

(2) comments

The MS Wire

Who is the "Meeks" to whom you refer, and quote, about two-thirds of the way into this article? There is no first reference.

Guest

Lisa Meeks, PhD, University of Michigan https://medicine.umich.edu/dept/family-medicine/lisa-m-meeks-phd

Welcome to the discussion.

Keep it Clean. Please avoid obscene, vulgar, lewd, racist or sexually-oriented language.
PLEASE TURN OFF YOUR CAPS LOCK.
Don't Threaten. Threats of harming another person will not be tolerated.
Be Truthful. Don't knowingly lie about anyone or anything.
Be Nice. No racism, sexism or any sort of -ism that is degrading to another person.
Be Proactive. Use the 'Report' link on each comment to let us know of abusive posts.
Share with Us. We'd love to hear eyewitness accounts, the history behind an article.