News about Long Covid including its relationship to ME/CFS 2020 to 2021

https://twitter.com/user/status/1368242130624385029

 

Summary of how Covid affects the body in the short and long term.

Source : https://www.chinadaily.com.cn/a/202007/31/WS5f237414a31083481725d51f.html

Edit : I've just noticed that men are covered by this picture, but women aren't. In other words, the testes and male fertility get a mention but ovaries and female fertility don't.

 

Well, it probably isn't the patients' opinion if the CFS clinics are anything to go by. As many of them.don't think it's possible for patients to be harmed by their treatments they don't record harms or outcomes.

 

And a right muddle it is too.

 

Yeah, same, just saw what you probably mean and yikes (and if not the same then double yikes). Ignore and/or block. Some people are just naturally unpleasant.

 

https://twitter.com/user/status/1368686995099316226

 

just came across this video on Youtube;

woman with ME who I'm guessing (from her description of what she is normally able to do) might be 'classified' as 'mild', but has had a relapse.
see around 9.00 where she says she gets chest pains, breathlessness.
Maybe a good example for Dr Pope and other LC who dismiss possibility of ME.

Code:

https://www.youtube.com/watch?v=3O7_2u9Ng6k

 

nbcnews.com
Opinion | Women are more likely to be Covid long-haulers. Here's why that matters.

https://www.nbcnews.com/think/opini...re-often-women-maybe-it-ll-change-ncna1259686

 

From the News from Scandinavia thread, about ME and long covid on the Swedish morning tv show Malou Efter Tio:

 

Overall a good article, but apparently the author didn't read Paul Garner's most recent BMJ blog post..

 

The Atlantic: Unlocking the Mysteries of Long COVID by Meghan O'Rourke

Quotes where ME is mentioned:

- The patients’ symptoms were too varied to be lumped under an established label; in some ways the condition resembled dysautonomia, and POTS in particular—but it was not textbook. (Some clinicians began calling it post-COVID POTS.) In other ways, it closely resembled myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), in which people alsodemonstrate exercise intolerance and profound fatigue, but it was likewise not textbook. Same for autoimmune disorders. A commonality stood out: These are all poorly understood conditions that, evidence suggests, can be triggered by the body’s response to infections, with clusters of system-roaming symptoms that get grouped under one name.

...

- IF THERE IS any reason for hope in the growing epidemic of long COVID, it is that some academic medical centers are taking these patients seriously and tailoring treatment to them. Medicine’s history with hard-to-identify chronic illnesses, particularly those that mainly affect women, has not been a good one. For decades now, marginalized patients who have felt mysteriously unwell—with ME/CFS, with post-treatment Lyme disease syndrome, with Ehlers-Danlos syndrome, and more—have banded together into activist groups to try to legitimize their suffering. The same is happening online in the long-hauler groups, which are full of patients who have been met with disbelief by local physicians. But the Mount Sinai doctors (along with collaborative teams in various other academic centers) have responded promptly to the problem. Recently, the NIH and the World Health Organization recognized long COVID as a syndrome that warrants more research.

...

- Doing better by these patients has been challenging because 20th-century medicine was not really built to treat hard-to-measure systemic illnesses—especially those, like dysautonomia, ME/CFS, and autoimmune diseases, that can be worsened by stress. Instead, it was based on the rather incredible notion that all bodies respond roughly the same way to infection or injury, and the immune system is a well-organized defense mechanism that never attacks the body. This perspective is turning out to be oversimplified.

...

- “I wouldn’t be surprised if people are walking about with long Epstein-Barr virus, or long influenza. We all know someone who is low energy, who’s told to work harder. We have all heard about chronic-Lyme sufferers, and those with ME/CFS. But they get written off,” Spencer told me. The difference now is that it is happening “on such a huge scale—unlike anything we’ve seen before. It is harder for the medical community to write off.”

 

Sorry don't now how to copy from Twitter so just a screen grab.
But what on earth is she saying?

Not important but she is a prehistorian and her Twitter name is preshitorian.
Is that a typo or is she being ironic?

 

Codswallop?

 

She appears to believe that ME sufferers believe in a postviral disease, while in her eyes long covid is viral and not postviral.

Also, the reason there has been lumping in ME is not for the lack of trying to split, but due to an inability to do so in a meaningful way.

 

Thanks for the translation into english @strategist

 

Q fever fatigue syndrome appears to be an instance of a postviral syndrome that wasn't lumped in with ME/CFS and this doesn't appear to have helped them make any scientific progress.

 

Bloomberg article:
Long Covid Is a Debilitating Mystery. Here’s What We Know

https://www.bloomberg.com/opinion/a...-s-what-we-know-about-covid-s-lasting-effects

The parts about ME/CFS:

 

UK: Parliamentary hearing on long Covid and the need for it to be recognised as an occupational disease.

This took place today and is available on YouTube

Code:

https://youtu.be/XK5Jz4Yqr8A

https://www.youtube.com/watch?v=XK5Jz4Yqr8A

Lucibee was presumably watching it and has tweeted some selected quotes, including this

and the APPG for Long Covid account tweeted this

 

Do you have cases with severely affected LC people comparable with very severe ME? (completely bedbound, extreme sensitivity to light, sound, touch etc.)?

 

I remember someone with LC in my own group who was completely bedbound first but then improved a lot. I saw some people who said walking is way too much for them. I don't know how common this is, it may not be. But when I came down with post-viral fatigue after glandular fever, I spent a lot of time on a gf forum and I remember reading everything but never commenting, because I didn't have the cognitive energy. People more severely affected may be less communicative and seemingly less present, who knows. Time will tell. But in general, this seems to be rare in the group.

I haven't really seen people with sensory sensitivites but I think Scheibenbogen's recent study of people with LC mentioned that they found some people with that.

Edit: From that study:

https://www.medrxiv.org/content/10.1101/2021.02.06.21249256v1