Long Covid in the media and social media 2023

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Long Covid's Cruelest Symptom: Homelessness
https://www.rollingstone.com/cultur...homeless-chronic-illness-gig-economy-1312460/
Cold weather is brutal for Wendi Taylor. After living with long Covid for two years, she knows that when the temperature drops, the pain and discomfort increases. This is especially true because of the severe arthritis in her hands, which only developed following her initial Covid-19 infection.

Taylor, who lives in Houston and is among the estimated millions of Americans living with long Covid, says that doing dishes during cold weather is probably the hardest part about living in the makeshift cabin she built from tarps and an 8×8 metal pop-up awning frame she found in the garbage.
 
that was a heartbreaking article. ME is mentioned briefly:

But if the challenges people living with other chronic conditions — like myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), fibromyalgia, and chronic lyme disease — have faced attempting to get workplace accommodations are any indication, those living with long Covid are in for a bumpy ride. “The disability system in this country has been slowly eroding for a long time now,” says Emily Taylor, vice president of advocacy and community engagement for #SolveME — a research and advocacy organization focused on ME/CFS and other long-term chronic illnesses — and a senior staffer at the Long Covid Alliance. “I, as an ME/CFS advocate, want to apologize to all the long-Covid folks and say, ‘If we had made more progress, you would be in a better place right now.’ ”
 

When unhoused individuals do have the chance to see a doctor, instead of appropriate medical attention and care, Taylor says, they’re given an unsolicited, uninformed lecture. “We’re told to try harder, patronizingly ‘educated,’ referred to mental health services, and given unhelpful advice to make lifestyle changes — which are often the result rather than the cause of our position,” she explains. “And then, when all that fails? [We’re] written off as choosing to be in this situation.”

While it’s no secret that the American health care system is broken, many people are still unable to let go of the toxic “bootstrapping” mentality: that anyone who works hard enough and sufficiently contributes to society is able to access the medical care they need.

And, in addition to the disbelief that people living with long Covid continue to face from those who don’t acknowledge they’re actually sick, people who are also unhoused have to deal with endless judgment from others questioning how it’s possible to end up in that position when there are places like shelters, food banks, and free clinics providing assistance.

And though there’s still a lot to learn about what causes long Covid and how to treat it, Ranney says that those currently living with it need — and deserve — support right now. “We can’t wait for all the information to be accumulated [from studies] before we do something to help people who are experiencing its financial impact,” she says. “And it’s going to require some leadership on the part of the government, insurers, and forward-thinking employers to get there.”
 
"
Long COVID Now Looks like a Neurological Disease, Helping Doctors to Focus Treatments"



https://www.scientificamerican.com/...tments/?utm_source=pocket-newtab-global-en-GB
my heart sank at the opening sentence
"Tara Ghormley has always been an overachiever."
but it improves, (Nath contributes).
towards the end:
In addition to drugs, other types of therapies, including physical therapy, can help improve some symptoms. But people who experience PEM face a particular challenge when using movement therapies. Pittman says the exertion can make these patients feel worse. “We don't want patients to go to not moving at all, but sometimes the type of movement they're doing may be flaring their symptoms.” He notes that often PEM strikes young, previously healthy people who will say, “‘I need to push myself,’ and then they go way too far and get worse. Our job is to try to find that middle ground and then make that consistent over time, so they're not getting further deconditioned but they don't have the PEM, which has been shown to set them back.”
 
Is long COVID ‘psychogenic’? Challenging claims that the disease is ‘all in the head’
Ryan Prior | Open Mind Mag | February 28, 2023

In the early months of 2020 as Covid swept the world, I was a science writer with a mandate to tell the human stories of the pandemic.

I started reaching out to patients living through the aftermath of Covid, people who got sick and stayed sick. As leaders were telling the public that those infected with the virus would recover within a couple of weeks, I met dozens of survivors whose bodies gave a much different accounting of the facts. Each individual’s story seemed to echo the others, fitting a pattern and timeline apart from the mainstream narrative. Nationwide, millions were suddenly experiencing the same seemingly new disease, long Covid.

But for those following the science of chronic illness—and those who’d lived it themselves—the appearance of long Covid was as predictable as the rise of the morning sun. For several decades, scientists had been finding disruptions in the bodies of those with post-infectious conditions. The specific pathways are too numerous to comprehensively list here, but studies show they include weakened immune response due to low levels of virus-fighting natural killer cells and heightened inflammation driven by elevated levels of signaling chemicals called cytokines. The list of abnormalities also includes the reactivation of viruses previously dormant in the body and the dysregulation of cortisol, a hormone needed in order to properly respond to stress.

A host of infectious triggers, from SARS and Epstein–Barr virus to Lyme disease and strep, can set off the same constellation of disabling symptoms, including brain fog, unrelenting fatigue, and pain. Such infections can also make an imprint through sleep disorders, nerve damage, and air hunger, where you feel as if you can’t get enough air and struggle to breathe. In the worst cases, such patients experience disability on par with late-stage AIDS or congestive heart failure. Despite continued reports, patients with this presentation are routinely dismissed. If only their symptoms could be traced to a physiological cause, a whole class of illnesses currently labeled “medically unexplained” or “contested” would be routinely understood by mainstream medicine. And despite the utter tragedy of long Covid, our newest pandemic illness offers the opportunity for just that.

But instead of accepting evidence emerging from university labs and teaching hospital clinics devoted to the study of long Covid, a new movement has evolved to lump together these endlessly sick patients with others who don’t get well—including individuals with fibromyalgia, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), and persistent symptoms of Lyme disease. Rather than accepting the reality of our latest agonizing illness, a string of news articles, backed by a contingent of scientists, has begun to call long Covid “psychogenic”—all in the head. We are at a pivotal moment. With the Centers for Disease Control and Prevention (CDC) estimating that nearly one in five people develops long-term symptoms after a Covid infection, it is time to rise up and stop the gaslighting—the rejection of the latest research and the experience of patients. We must stop this dismissal before long Covid joins ME/CFS and persistent Lyme as just one more contested disease.

https://geneticliteracyproject.org/...ms-that-sufferers-disease-is-all-in-the-head/

eta: mods, maybe this should be in its own thread to increase exposure.
 
Wish people gave accounts of how they reacted to the gaslighting. If someone treated me like that I'd explain the scientific consensus on ME, and walk out.

Once a doctor tried to blame my symptoms on inactivity, and I straight up roasted her in a MyChart message:
This is textbook medical gaslighting. I need you to treat me with respect instead of assuming I'm lazy and stupid while spouting medical misinformation. I've been hearing variations of this for half a decade now. It's systemic, it's ableist, and I'm sick of it.

You're claiming my main symptom is fatigue, but it's actually PEM. Deconditioning can't explain PEM or ME/CFS. (e.g., NY DOH info or Bateman et al 2021 in Mayo Clinic Proceedings) I'm also stunned by your assumption I don't exercise enough. I take walks a few times a week, which is as much physical activity as I can tolerate. Doing as much as you can tolerate is what the CDC recommends for ME/CFS. And it's not like I haven't tried and failed multiple times to exercise my way out of this disease. Telling me to blindly exercise more is not the standard of care, it's quackery.

I'm also flabbergasted that you refuse to call my disease ME/CFS, the name used by the CDC, the NIH, and 95% of papers I read. Regardless, the name you use is unimportant.

Namely, my request is that my illness is coded in my chart as G93.32, as opposed to R53.82, which excludes CFS. If not, please inform me in writing that you refuse to code my diagnosis properly. Thank you.

It's my policy that whenever a doctor tries to gaslight me, I rebuke them and ditch them.
 
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Medpage today
Evaluating and Treating Children With Long COVID

Quotes (my bold):

Given the overlap between post-COVID condition symptoms and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), the collaborative has suggested screening for ME/CFS.

Often the "pattern of fatigue" in children may be similar in both conditions. Morrow noted some children may not meet the 6-month threshold or "full criteria" for ME/CFS.

...

Treatment for systemic or constitutional symptoms of post-COVID conditions should include the following:

  • Addressing medical causes of fatigue -- for example, treating anemia with iron supplements
  • Implementing "lifestyle modifications" such as ensuring adequate nutrition, hydration, and sleep
  • Gradually increasing physical activity or "pacing" as tolerated, while staying alert to possible post-exertional malaise
Patients often require a multidisciplinary approach that leverages a range of traditional therapies -- such as pediatric rehabilitation, physical therapy, occupational therapy, and mental health therapy. Some complementary therapies -- such as yoga, Tai Chi, acupuncture, massage, and meditation may also help with fatigue.
 
Medpage today
Evaluating and Treating Children With Long COVID

Quotes (my bold):

Given the overlap between post-COVID condition symptoms and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), the collaborative has suggested screening for ME/CFS.

Often the "pattern of fatigue" in children may be similar in both conditions. Morrow noted some children may not meet the 6-month threshold or "full criteria" for ME/CFS.

...

Treatment for systemic or constitutional symptoms of post-COVID conditions should include the following:

  • Addressing medical causes of fatigue -- for example, treating anemia with iron supplements
  • Implementing "lifestyle modifications" such as ensuring adequate nutrition, hydration, and sleep
  • Gradually increasing physical activity or "pacing" as tolerated, while staying alert to possible post-exertional malaise
Patients often require a multidisciplinary approach that leverages a range of traditional therapies -- such as pediatric rehabilitation, physical therapy, occupational therapy, and mental health therapy. Some complementary therapies -- such as yoga, Tai Chi, acupuncture, massage, and meditation may also help with fatigue.

Time is a flat circle. GET is now pacing, and don’t forget to throw in some acupuncture. The evidentiary double standard is so blatant, and the people charged with enforcing rigorous compliance eat this nonsense up
 
Medpage today
Evaluating and Treating Children With Long COVID

Quotes (my bold):

Given the overlap between post-COVID condition symptoms and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), the collaborative has suggested screening for ME/CFS.

Often the "pattern of fatigue" in children may be similar in both conditions. Morrow noted some children may not meet the 6-month threshold or "full criteria" for ME/CFS.

...

Treatment for systemic or constitutional symptoms of post-COVID conditions should include the following:

  • Addressing medical causes of fatigue -- for example, treating anemia with iron supplements
  • Implementing "lifestyle modifications" such as ensuring adequate nutrition, hydration, and sleep
  • Gradually increasing physical activity or "pacing" as tolerated, while staying alert to possible post-exertional malaise
Patients often require a multidisciplinary approach that leverages a range of traditional therapies -- such as pediatric rehabilitation, physical therapy, occupational therapy, and mental health therapy. Some complementary therapies -- such as yoga, Tai Chi, acupuncture, massage, and meditation may also help with fatigue.
"While staying alert to" - how exactly . If you provoke PEM you could be on a slippery slope. Kids could be in rolling PEM without realising the significance - it's very hard to get kids to rest.

Any objective measures like heart rate monitoring to help assess, define and help manage/ avoid PEM .
Or is this too much to expect ?
 
Unable to access, would be curious to read.

New Scientist: "Long-neglected chronic conditions finally come into the spotlight"

'Growing evidence that long-term conditions like myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and fibromyalgia are caused, wholly or in part, by viral infections is good news for millions of people'


https://www.newscientist.com/articl...c-conditions-finally-come-into-the-spotlight/
 
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