What do you guys think of CFS health? The guy from Australia that says he has a 91% success rate?
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
Anyone mild or moderate get muscle twitching?
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
Was mild and crashed 7 weeks ago and now I barely can function. The brain inflammation is back and I can’t seem to build my baseline. Has this happened to anyone? Did you stay in the crash with a lower baseline or eventually come out of it? Feels never ending and evolving :(
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
1.5 years severe than 6 months mild now have been in a big crash for 25 days. I’m really worried, when I was mild I never had a crash like this and barely even crashed at all. This crash doesn’t seem to be lifting and yesterday I felt so concussed. I hope I’m not moderate or severe now.
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
12th day of this crash. Woke up feeling poisoned in my brain and tight chest. Before this I hadn’t had pem in 2.5 months and I was “mild”. I’m worried this crash is going to lower my baseline. Has anyone mild had a bad nuero crash and got back to baseline after weeks?
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
I think my bf has bpd and I need help.
r/BPD is a community of people with BPD (EUPD) and people who know someone with BPD looking for mutual support and resources to help guide them through their journey.
Hello everyone. I was bedbound with Long Covid/ME/CFS for 1.5 years. In October I started Ativan and Ivabradine and went from 5% function to 70%. It was a miracle. The last 4 months I didn’t have any PEM, I could go out everyday. Continued below
For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
Hi what could this mean ?
A place to post and discuss issues related to Adrenal Insufficiency. Appropriate for anyone with Addisons, Cushings, Congenital Adrenal Hyperplasia, Panhypopituitarism, ALD. Persons taking steroids for any condition including cancer, asthma, allergies or those suffering from any Pituitary, Thyroid, or Adrenal disease. All are welcome!