ME/CFS (kbin)

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A place on kbin.social for those with ME/CFS. I made this during the reddit migration, just in case any of those with ME/CFS need a magazine on kbin. Posts, resources etc welcome. Check out our Microblogs section - a good way to get more fediverse content! If you are looking for basic resources, e.g. me/cfs organizations or fact sheets, there are some over at: - link for kbin = @[email protected]

link for lemmy= [email protected]

founded 1 year ago

The Nicotine Patch Long COVID, ME/CFS and Fibromyalgia - Health Rising (www.healthrising.org)

submitted 11 months ago by [email protected] to c/[email protected]

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I'm actually willing to try this out. The risk seems low enough and I don't have anything else to do.

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[–] [email protected] 1 points 10 months ago (1 children)

Have you been trying it?

[–] [email protected] 1 points 10 months ago (1 children)

Yeah, I'm currently more or less in the middle of the first phase. I'm feeling more woozy than usual. Apart from that I don't feel much better or worse.

I'll make a post about my experience when I'm finished with the first round. I've also done short bursts of how I'm feeling in German on my blog https://bjoern-tantau.de and on Mastodon @[email protected].

[–] [email protected] 1 points 9 months ago

Thank you!

[–] [email protected] 1 points 11 months ago

an actual meta study about the subject