this post was submitted on 17 Oct 2024
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[–] HobbitFoot@thelemmy.club 24 points 4 weeks ago (17 children)

CFS is a syndrome rather than a disease because, until recently, it only presented as symptoms instead of as an identifiable problem with a person. I know that a some people who get diagnosed for CFS get later diagnoses as neurological disorders like multiple sclerosis.

It sounds like the more powerful MRI scanners are seeing inflammation in the rest of those suffering from CFS.

That would mean CFS is a lifelong degenerative condition.

[–] Neurologist@mander.xyz 28 points 4 weeks ago* (last edited 4 weeks ago) (12 children)

Hey I’m a researcher who works on ME (in the past called CFS).

ME/CFS is currently classified as a disease/biological illness according to the CDC.

ME is a disease state in itself. We don’t know much about it, but it can’t be explained by other diagnoses, as the defining factor, neuro-immune abnormalities including immune activation showing up post exertion is unique to it. You’re completely right that we don’t yet have a reliable biomarker. We have a test that differentiates from healthy controls, but it was discontinued for ethical reasons because conducting the test leads to a sometimes permanent worsening of the illness.

In the past it’s been mixed up and jumbled a lot, but the picture is getting clearer.

There have been a few case reports of degenerative forms of the illness. But in general it takes a more classical relapsing remitting pattern. Although even in less bad stages some patients are severely functionally disabled, even bedridden and tubefed. It has a really wide range of severities with the least severely affected able to work part time and walk and travel, while the most severe might not even be able to communicate.

[–] i_love_FFT@lemmy.ml 3 points 4 weeks ago (7 children)

I have a friend who's now living with ME. Any resources for the general public to better understand the condition?

[–] Neurologist@mander.xyz 1 points 4 weeks ago (1 children)

For you to help your friend. Or for your friend themselves?

[–] i_love_FFT@lemmy.ml 1 points 4 weeks ago (1 children)

For me to be a better friend by better understanding his new limitations...

He already has a good support network, they organised a fundraiser to get him an electric wheelchair, which is awesome! But at first I didn't understand why it was helping him, because I don't know enough about the condition. 🫣

[–] Neurologist@mander.xyz 2 points 4 weeks ago* (last edited 4 weeks ago) (1 children)

This channel has a bunch of short (5 mins long videos) about ME to educate people.

There’s also a slightly outdated (but still worth the watch) oscar nominated documentary about it, which has been made free and put on youtube recently It’s Unrest by Jennifer Brea

One of my patients also runs this excellent website with a bunch of resources about the disease.

[–] i_love_FFT@lemmy.ml 1 points 4 weeks ago (1 children)
[–] Neurologist@mander.xyz 1 points 3 weeks ago (1 children)

if youve got to any, could you tell me what you think? It’s always useful to know what I should recommend to my patients to show their friends and family.

[–] i_love_FFT@lemmy.ml 1 points 3 weeks ago

I'm mostly a "wikipedia reader" type of person, so I don't have good pop sci sources to recommend... Sorry!

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