What r/cfs is talking about this week

That you may feel seen ♥️

Former Olympic sprinter Beth Dobbin discusses life with severe ME, the lack of specialist care and treatments, and her call for increased research funding. Includes a response from the Health...

Let's hear it for the people who had to lower our baseline to vote in the US this election, whether that meant waiting in line in person, or making a half dozen calls to get a mail-in ballot and...

Maybe we have some new congresspeople who will pay attention to our struggle? Fingers crossed

ME/CFS patients battled for recognition as researchers struggled for funding. The pandemic finally gave science the scale to start finding answers.

I am severe and housebound, and currently on an extended period of extreme rest to try and improve my capacity a little. My pet pigeon Hallie is the perfect CFS companion. All she really wants is...

Also here it is on TikTok in case you want that link: https://www.tiktok.com/t/ZTPR9g4ES/ (warning that there's audio)

TL;DR Here's my new bedside setup! More details are listed below, but the gist of it is that I can reach different zones of the shelf at different times of the day :) I'm happy with it! I've been...

Just wanted to share. SSI backpay pulled through. They give you your backpay in 3 checks 6 months apart, so I made it my goal to overhaul this with my first backpay check. Most of the budget went...

Found this on r/Migraine and thought I’d repost here:)