Long Covid in the media and social media 2022

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I don't think we can judge what is best for her from a short media article.
Losing movement from one side may result from a stroke. We don't know whether she has PEM.
True, but near the end of the article she is quoted as saying:

"Just keep positive because if you don't keep positive you can't get anywhere," she said. "Just keep going even if it gets tough. Just keep going because in the end, you will be able to do it."

Exactly what shouldn't be advised in the case of ME.
 
Time Magazine -

Why You Should Rest—a Lot—If You Have COVID-19

https://time.com/6215346/covid-19-rest-helps/

Time Magazine said:
Until recently, running was a major part of Emma Zimmerman’s life. The 26-year-old freelance journalist and graduate student was a competitive distance runner in college and, even after she graduated, logged about 50 miles per week. So she tentatively tried to return to her running routine roughly a week after a probable case of COVID-19 in March, doing her best to overcome the malaise that followed her initial allergy-like symptoms. Each time, though, “I’d be stuck in bed for days with a severe level of crippling fatigue,” Zimmerman says.

Months later, Zimmerman still experiences health issues including exhaustion, migraines, brain fog, nausea, numbness, and sensitivity to screens—a constellation of symptoms that led doctors to diagnose her with Long COVID. Though she can’t know for sure, she fears those workouts early in her recovery process may have worsened her condition.

“I had no idea that I should try to rest as hard as I needed to rest,” she says.

...

Researchers are still learning a lot about Long COVID, so it’s impossible to say for sure whether rest can truly prevent its development—or, conversely, whether premature activity causes complications. But anecdotally, Friedly says many of the Long COVID patients she sees are working women with families who rushed to get back to normal as soon as possible. It’s hard to give one-size-fits-all guidance about how much rest is enough, but Friedly recommends anyone recovering from COVID-19 stay away from high-intensity exercise for at least a couple weeks and avoid pushing through fatigue.

For people who have already developed Long COVID, rest can also be useful for managing symptoms including fatigue and post-exertional malaise (PEM), or crashes following physical, mental, or emotional exertion. The U.S. Centers for Disease Control and Prevention recommendspacing,” an activity-management strategy that involves rationing out activity and interspersing it with rest to avoid overexertion and worsening symptoms.

In an international study published last year, researchers asked more than 3,700 long-haulers about their symptoms. Almost half said they found pacing at least somewhat helpful for symptom management. Meanwhile, when other researchers surveyed about 500 long-haulers for a study published in April, the overwhelming majority said physical activity worsened their symptoms, had no effect, or brought on mixed results. That may be because long-haulers have impairments in their mitochondria, which generate energy cells can use, recent research suggests.

Before Long COVID existed, researchers and patients encouraged rest and pacing for the management of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). The condition’s hallmark symptoms include PEM and serious, long-lasting fatigue—diagnostic criteria that many people with Long COVID now meet. A study of more than 200 people with Long COVID published in January found that 71% had chronic fatigue and almost 60% experienced PEM.

For years, clinicians tried to treat ME/CFS patients by gradually increasing their physical activity levels. But that practice has since been shown to be not only ineffective, but often harmful, because people with ME/CFS “have a unique and pathogenic response to overexertion” due to cellular dysfunction, explains Jaime Seltzer, director of scientific and medical outreach at the advocacy group MEAction. Most people with ME/CFS prefer pacing over exercise-based therapy, one 2019 study found.

That last sentence in the quote -- saying that people with ME/CFS "prefer" pacing to GET -- is very strange. It feels like "both sides" reporting, positioning both treatments as having the same level of evidence/effectiveness and it's simply up to the patient to choose the one they prefer.

And they even include a link to this 2019 study (my bolding):
Findings from analysis of primary and secondary surveys suggest that cognitive behavioural therapy is of benefit to a small percentage of patients (8%-35%), graded exercise therapy brings about large negative responses in patients (54%-74%), while pacing is the most favoured treatment with the lowest negative response rate and the highest reported benefit (44%-82%).

It's quite a stretch to turn that sentence into "most people prefer pacing" which sounds like it's simply a matter of taste.
 
Until it happens to you.
More of this needed


It really highlights how good people can ultimately be forced into treating patients badly and endangering them with systemic choices they have no power or control over. The medical environment is what is broken and quite a few of these choices forced were bad doctoring but also by funding and administration. The level of reform necessary to finally get patients the proper care is not coming any time soon.
 
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Blood test could identify long-COVID risk and allow early intervention
If the experimental test is validated by further research it may result in people at high risk of long-COVID being given anti-viral treatments in the hope of preventing debilitating symptoms.

A blood test done while people have COVID could predict whether they're likely to develop long-term health problems, a new study suggests.

If the experimental test is validated by further research it may result in people at high risk of long-COVID being given anti-viral treatments in the hope of preventing debilitating symptoms.

Researchers at University College London compared levels of more than 90 blood proteins in 54 healthcare workers with COVID and a control group of healthy staff.

They found several proteins were dramatically disrupted for up to six weeks, even in those with mild symptoms, according to results published in the journal Lancet eBioMedicine.

Twenty of them were predictive of persistent symptoms a year later. Most were linked to anti-clotting and anti-inflammatory processes.

The researchers then used an artificial intelligence (AI) algorithm to scan proteins in the blood samples - and successfully identified the 11 infected health workers who developed long-COVID.

Dr Wendy Heywood, one of the senior researchers from UCL's Great Ormond Street Institute of Child Health said: "If we can identify people who are likely to develop long-COVID, this opens the door to trialling treatments such as antivirals at this earlier, initial infection stage, to see if it can reduce the risk of later long-COVID."

https://news.sky.com/story/blood-te...id-risk-and-allow-early-intervention-12706671

Study thread here:
https://www.s4me.info/threads/plasm...sars-cov-2-infection-captur-et-al-2022.29710/
 
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At least the President of the Australian Medical Association has his eyes open (as well as a decent meme game).


First we had thoughts and prayers. Now we have memes. Still no walk, though, but the talk is up-to-date.

"Person best-placed to do something asks other people to do something, anything" has always been one of my favorite tropes. That's leadership you can count on... as long as you don't expect them to do anything. Memes, though. Oh, the memes.
 
The Scientist Multiple Possible Causes of Long COVID Come into Focus

quotes:

Taken together, studies suggest that long COVID and its many symptoms may not have just one cause, and may not be just be one disease. “There may not be a single mechanism for all long COVID—there could be multiple mechanisms ongoing, and for some individuals one may be more dominant than the other,” says Nath.

...

Another immune-related hypothesis for long COVID, which Nath says doesn’t necessarily preclude inflammation-related symptoms, is that the body starts targeting itself. Long COVID shares symptoms with some suspected autoimmune diseases—mainly ME/CFS, which is marked by post-exertional malaise and muscle pain—and multiple studies have found that long COVID patients develop self-antibodies that persist for a year, and perhaps longer.
 
I highly doubt there's a single mechanism for all of long Covid. It's just too heterogeneous. I see it as an umbrella term for any health problem caused by Covid. There's no way someone who's constantly breathless has the same problem in their body as someone who gets ME, for example. Well-defined but inclusive subtypes of LC would be welcome.
 
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