The MRC (UK) strongly encourages more research to better understand this condition.’ Dr Neha Issar-Brown #MEAwarenessWeek#millionsmissing https://t.co/o5FBH9q01d
Chronic Fatigue Syndrome is a very debilitating syndrome which affects about 1 million Americans' Dr. Ashton https://t.co/o5FBH9q01d #cfs#MEAwarenessWeek
Don't look f someone who helps you feel better. Lk for someone who helps you feel more' @RaphaelCushnir who lives with ME/CFS. K: You can of course do both.
🥁 Today is #MEAwarenessDay. Advocacy often struggles to make an impact outside the patient community. Please share this short video about #MyalgicEncephalomyelitis, aka #MECFS, with your followers. Ty for your support. 🤝 https://t.co/36IZzfwUJl
Simon McGrath has written a really good blog on the new government-funded DNA sequencing work for #MECFS.
Simon writes excellent, accessible blogs on #MECFS research, and is well worth a follow. I was happy to help out with the video.
https://t.co/6QZLe8Es2q
I’m really glad to hear about this government funding into ME.
I’ve had mild ME for a while now. It’s been a long, expensive road to improve.
My heart goes out to those who are severely affected and anyone with it. There are so many out there being neglected by the NHS and given very bad advice about treatment, that’s if they get diagnosed at all.
The condition is hard because you have the double whammy of physical symptoms paired with it being so misunderstood (which I do understand a bit - because unless you have it, you can’t really get it).
People need to understand that it is a condition of mitochondrial dysfunction rather than “I’m really tired”. Your energy production is f**ked at a cellular level.
Anyway I digress but good news:
https://t.co/YFt7KVhnqd