Black Covid long-haulers say doctors dismissed their symptoms, so now they’re relying on one another for support
Black-led groups have popped up across the country as more and more Black people have reported long Covid symptoms — and difficulty getting treatment.
Chimére L. Smith, 40, thought her bout with Covid in March 2020 would pass within two weeks, as most mild cases do. But the Baltimore English middle school teacher found herself continuously experiencing extreme fatigue, diarrhea, dry mouth, brain fog and a sore throat, which she initially attributed to a possible sinus infection. By April, she couldn’t work or drive, had lost 30 pounds, had spinal pain and lost complete vision in her left eye. She even thought about taking her own life. Smith was experiencing long Covid.
Smith said she visited hospitals a dozen times seeking help, but the physicians brushed her off, and one doctor labeled her “aggressive” when she insisted that severe headaches she experienced were due to Covid. She said she was repeatedly discharged with no resolution after each visit.
Researchers explore solutions for Covid long haulersApril 16, 202206:10“I would come in with notes of my symptoms and share these symptoms with these doctors and they would not hear me. They wouldn’t listen to me. They would treat me as if I was a child and I didn’t know my body,” Smith said. “I wanted to die because I could not eat. I could hardly drink. I couldn’t think. Everything that I knew about my life within those first two or three months had been destroyed.”
That’s when Smith found the BIPOC Women Long Covid ‘Long Hauler’ Support Group, a Facebook group with hundreds of women of color with long Covid who meet virtually. Since joining the group in May 2021, Smith said she has been better equipped to advocate for her own care and that of Black women living with prolonged symptoms of the virus. She’s one of many Black people across the country suffering from long Covid who have found solace in communities of people having the same experience. Similar support groups have popped up in many states since the pandemic began, with Black people uniting to tackle everything from lingering symptoms to disparities in the nation’s health care system.
Chimere Smith.Courtesy Chimere SmithLong Covid — or post-Covid — was first identified in the U.S. in the months after the pandemic began in March 2020. And now, two and a half years into the public health crisis, a lot remains unknown about the prolonged illness that affects up to 23 million Americans. Symptoms of long Covid vary from person to person, with people reporting experiencing everything from fatigue and cognitive impairment to tissue damage and organ injury, according to the U.S. Government Accountability Office. Like most of the pandemic’s fallout, Black people are bearing the brunt of long Covid, with the group making up a majority of long Covid hospitalizations and researchers even projecting that Black people’s life expectancy will drop significantly in the next five years as a result. As a way to counter the troubling data, Black people have formed these support groups in hopes of making sense of the illness and to find the help they need.
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