PART 1: Instructions to Take Action
To All ME/CFS –S.E.I.D. Patients, Family and Friends,
As most patients know the IOM and NIH P2P have released some positive findings in our disease. While there Read more [...]
(Dr. Peterson speaks to the Swedish Parliament and years of effort in Holland culminate in the delivery of a petition to have ME/CFS be considered and treated as a biomedical disease in blogs by Anne Ortegren and Esme de Groot.)
Dr Peterson in Sweden
by Anne Ortegren
Dr Peterson and Gunnar 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 [...]
What happens when you get three of our most experienced physicians together in a Roundtable setting and have patients lob questions a them?....Lots of interesting discussion.
Check out Part I of a series on Simmaron's FDA Roundtable meeting as Dr. Peterson, Dr. Klimas and Dr. Enlander talk about Read more [...]
The FDA has somehow missed the fact that Dr. Daniel Peterson is an ME/CFS expert clinician/researcher. For over 30 years now, Dr. Peterson has been treating ME/CFS patients in Incline Village, Nevada, with a variety of treatments. Earlier today ME/CFS patients were told that FDA has not invited Dr. Read more [...]
Dear Patients, Patient’s Loved Ones and Friends,
Since I ended my hunger strike, I have learned that the FDA has sent invitations for the ME/CFS scientific stakeholder workshop scheduled for April 25-26th. The FDA hasn’t disclosed who it is inviting, and did not solicit input from patients. You, Read more [...]