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 Times They Are a Changing.
In response to Dr. Unger's request, the Simmaron Research Foundation is sponsoring a large workshop at the IACFS/ME Conference to recommend immune tests that will guide the diagnosis and treatment of chronic fatigue syndrome.
Getting the CDC's stamp of approval Read more [...]
It's not often that ME/CFS luminaries such as Dr. Peterson, Dr. Klimas and Dr. Enlander sit down in public to talk about their approaches to ME/CFS treatment but that's exactly what happened at the Simmaron Round-table held at the FDA Workshop earlier this year.
Check out why Dr. Peterson Read more [...]
Bob Miller can't dance...he can't run...he can't even play baseball for ME/CFS - he's not strong enough for that but he can fall, and May 12th, ME/CFS International Day, he's going to fall a long way, very quickly, to raise money for ME/CFS research.
It's been a busy couple of months for Bob. Read more [...]