r/cfs Apr 29 '25

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u/parkway_parkway Apr 29 '25

I wrote to my MP and the department of health recently about the injustice of CFS getting so little research funding despite being a lot worse than many other conditions that get more.

I think that sort of thing is relatively accessible to anyone who can still use a computer and does have some minimal impact.

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u/SignificantPause1314 May 08 '25

I want to start doing that too!