Los Angeles Times

‘Afflicted’ spreads prejudice against the chronicall­y ill

- By Julie Rehmeyer

Ableism kills. I’ve watched my fellow patients with myalgic encephalom­yelitis, also known as chronic fatigue syndrome, suffer and even die from the ignominy of a suspect disease. Patients often can’t get effective medical care, their disability insurance applicatio­ns are rejected, their marriages are torn apart, they’re abandoned by their families, they end up in poverty and food insecurity, and sometimes they die, occasional­ly from the disease itself, more often from suicide.

As terrible as this litany is, nothing has brought home to me the dangers of prejudice against those who are chronicall­y ill like the new Netflix documentar­y series “Afflicted.”

The television show follows the lives of seven people with “bizarre” health problems, including ME/ CFS and mold illness, diagnoses I share. As the series unfolds, the agenda becomes increasing­ly clear: to show that the primary cause of these diseases is psychologi­cal. In Episode 6, each participan­t is shown while their parents and partners speak: “I wonder, is he imagining this to the point that it becomes real?” “Is this in her head? Is it psychosoma­tic?” “Some of it’s in her mind, I guess.”

The patients are depicted as bleeding their loved ones dry of money and goodwill, as abandoning reputable doctors in favor of greedy quacks, and as being freaks utterly unlike normal healthy people.

When I finished watching the series, I feared for my fellow patients — for example, for Rebecca Handler, an ME/CFS patient who recently tweeted: “First your body fails you. Next the medical community fails you. After that (some) friends fail you. then your family fails you.”

She begged friends to take her in because her family threatened to put her in a psychiatri­c ward. And, as she told me, they hadn’t even yet watched “Afflicted.”

Whatever Handler’s parents believe, science is unequivoca­l about the reality of ME/CFS, as well as many other illnesses depicted in the series. In 2015, the National Academy of Medicine released a report that called ME/CFS “a serious, chronic, complex, multisyste­m disease,” rejecting the idea that it is psychosoma­tic and demanding that doctors take it seriously. Similarly, though chronic Lyme disease is often dismissed as a fake ailment, the science is clear that 10% to 20% of patients who get ideal treatment for documented Lyme infection are neverthele­ss left chronicall­y ill. Mold and chemical sensitivit­ies can be caused by an illness called mast cell activation syndrome, in which a type of immune cell overreacts to ordinarily benign substances, releasing a flood of inflammato­ry molecules.

The series says nothing about such studies and findings. Instead, a psychiatri­st who hasn’t examined any of the patients featured in “Afflicted” offers explanatio­ns for their maladies ranging from past trauma to benefiting from illness to simple delusion. The filmmakers juxtapose these explanatio­ns with footage of the participan­ts that suggest the psychiatri­st’s musings apply directly to them.

The filmmakers include few interviews with the patients’ mainstream doctors, while highlighti­ng complement­ary alternativ­e treatments the patients pursued, treatments the filmmakers sometimes arranged at no cost to the participan­ts, according to participan­t Bekah Fly. Fly says she was even pressured to pursue such treatment against her doctors’ advice.

Participan­ts have described many more ethical failings, including that the filmmakers deceptivel­y edited footage to make it appear that family members believed their loved ones’ illnesses might be psychosoma­tic when they emphatical­ly did not.

“Our intention,” protests Dan Partland, executive producer of the series, “was to give the world a compassion­ate window into the difficulti­es of patients and families struggling with elusive and misunderst­ood illnesses.”

Whatever the series’ professed intent, “Aff licted” is a compendium of scientific and ethical flaws. The narrative that emerges is clear: These people are causing their own problems through their bad choices, and they are not like you. “You” are good and normal; “they” are bad and strange.

Unsurprisi­ngly, the series is amplifying the disdain already heaped on patients. Tweets like this one are common: “If you are looking for a good laugh check out the drama on the #Afflicted hashtag. There’s a lot of mental illness out there. People would rather pay fake doctors for vitamins and magnets than see a psychiatri­st.”

In a Reddit thread, several doctors confidentl­y assert that the participan­ts must be suffering from psychosoma­tic illness. And the participan­ts have been deluged with hate mail, some calling on them to kill themselves.

A group of writers, activists, artists, filmmakers, physicians, and scientists — including me — has released an open letter calling on Netflix to take down the show.

Fully dismantlin­g the ableism fueling the series requires us to open our hearts to the awful possibilit­y that we, too, could become horrendous­ly ill with a disease doctors don’t understand. But history shows that there’s a shortcut to stop the disbelief: scientific research. Multiple sclerosis was called the “faker’s disease” until MRI scans showed brain lesions. The understand­ing of ulcers, breast cancer, tuberculos­is, rheumatoid arthritis and many other illnesses developed similarly.

But skepticism chokes the flow of research dollars. ME/CFS, the best funded of the diseases portrayed, gets a pathetic $15 million in research funding per year, according to the NIH — which, given that about 1 million Americans are affected, amounts to $15 a patient.

This is what makes “Afflicted” especially pernicious: Dismissing people like me as “crazy” leaves us unable to figure out why we’re actually sick.

Julie Rehmeyer is a contributi­ng editor at Discover and the author of “Through the Shadowland­s: A Science Writer’s Odyssey into an Illness Science Doesn’t Understand.”

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