The most important treatment trail in the history of ME/CFS has begun. Take a close look at the huge Rituximab trial that could change how ME/CFS is treated and viewed as Fluge and Mella tell us about it, the many substudies embedded in it and why they think ME/CFS may be an autoimmune disorder in Read more [...]
As things stand right now, one could say that it takes 20 years to get 1 year’s worth of ME/CFS research done. Why? Because the level of funding allocated for ME/CFS research is 20 times lower than that of comparable diseases.
See “The Underfinanced ME/CFS Research, Pt I - Facts and figures Read more [...]
The next topics in the ME Associations De Meirlier ME/CFS experts video series were two big ones; 'Treatment' and 'Remedy and Hope'. You can't hope to cover the panoply of chronic fatigue syndrome (ME/CFS) treatments in a short video but the ME Association team pointed Dr. De Meirleir in some Read more [...]
We're stuck in the doldrums as the federal level with little funding and little support but that doesn't mean stagnation. With several major studies wrapping up 2013 will be a very important year for this disorder. Check out some of the events and studies to look forward to this year.
FDA Decision Read more [...]
The information found on Health Rising is mostly put together by people with ME/CFS and/or FM.
It is not intended as medical advice and should be used for informational purposes only.