this post was submitted on 17 Oct 2024
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[–] i_love_FFT@lemmy.ml 3 points 1 month ago (2 children)

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

[–] Vex_Detrause@lemmy.ca 3 points 1 month ago

This Podcast Will Kill You EP 137: ME/CFS did a great episode. They also have their sources so if you need a deeper dive you can read the articles.

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

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

[–] i_love_FFT@lemmy.ml 1 points 1 month 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 1 month ago* (last edited 1 month 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There’s also a slightly outdated (but still worth the watch) oscar nominated documentary about it, which has been made free and put on youtube recently It’s Unrest by Jennifer Brea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 1 month ago (1 children)
[–] Neurologist@mander.xyz 1 points 1 month 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 1 month ago

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