I’m looking for a short (no more than 20 minutes) exercise program, preferably a video, that would be safe for ME/CFS. Can anyone recommend a program, maybe Pilates, yoga, or tai chi? I walk a ...
https://www.healthrising.org/forums/threads/safe-exercise-for-me-cfs.6863/
Is anyone testing this gadget? Would love to hear about how it’s going, if you are allowed to comment publicly. (I know companies sometimes ask people not to comment when testing beta versions ...
https://www.healthrising.org/forums/threads/stat-device.6837/
Greetings! Looking for Recruiting participants: We are working on a research project which aims to explore the impact of chronic fatigue syndrome ME/CFS on identity construction among young a...
The AVA A Vagus Adventure private facebook page (a great resource) has just announced funding for a feasability study on VNS for ME/CFS. "We are HUGELY excited to announce that after several at...
https://www.healthrising.org/forums/threads/new-vagus-nerve-stimulation-study.6859/
I’m not sure this is the right place to post this, but I just went to Florida to Nancy Klimas’s clinic and wanted to give you a report. I saw a different doctor, but the whole place was amazi...
https://www.healthrising.org/forums/threads/institute-for-neuro-immune-medicine.6861/
Hi, I was recently diagnoised with ME/CFS. I have gone from a high functioning, very active person, to basically home bound. Are there any medications or supplements that have helped you? I am ...
https://www.healthrising.org/forums/threads/do-any-medications-supplements-help.6806/
Dr. Lonsdale will be a hundred years old April the 22 (born 1924). Collecting thank yous, congratulations and well wishes to a Google form, collated and sent to Dr Lonsdale. If you haven't yet ...
Stoo Brown submitted a new resource: Poo Transplant resolved my ME :-) - The Power of Poop > I am a 53 year-old white British male living in Scotland. > I had ME for ten yea...
https://www.healthrising.org/forums/threads/poo-transplant-resolved-my-me-deleted.6484/
Trigger Warning! Please help a fellow ME sufferer by signing the following petition and sharing if you are able: SIGN THE PETITION Save Millie's life - Royal Lancaster Infirmary must STOP c...
My ME entailed high blood nagalase causing loss of six teeth due to reinfection of past root canals and getting infections from simple cuts. I'm curious if CFS/ME patients are dying from Covid at...
https://www.healthrising.org/forums/threads/any-news-on-how-cfs-patients-are-doing-with-covid.6339/
I've noticed over the 8 years of my ME/CFS, the few times I've taken antibiotics for about a twice-a-year UTI, I feel less fatigue. Not every time, but maybe 30% of the time. I don't feel any mor...
hi! new to this forum but been reading the blog & all your comments for months - been a tremendous help as I try to get a diagnosis and care for my CFS-like symptoms. much gratitude! I was just...
https://www.healthrising.org/forums/threads/anyone-a-patient-with-rthm.6744/
Decades ago I experienced a year of chronic fatigue due to exposure to an industrial solvent called trichloroethylene. Years ago I was able to find research identifying specific changes which the...
https://www.healthrising.org/forums/threads/microbiome-in-cfs-and-me.6855/