(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...
(As CFSAC kicks off its abbreviated session in webinar form, Ken Friedman looks back at ten years of CFSAC and asks what it has accomplished. Ken Friedman’s own time on CFSAC in the early 2,000’s was highlighted by his dissenting report “Fish Or...
(An earlier version of this blog appeared on Phoenix Rising) ‘Let the Patient Revolution Begin’ A militant cry from those difficult ME/CFS patients unwilling to listen to doctors, researchers and government departments who only have patients’ best...
The thirty-five is now fifty… Instead of being mollified by the DHHS working document, the effort by ME/CFS experts to rescind the IOM contract to produce a clinical case definition has actually gathered steam. The fifty ME/CFS experts signing the letter now...
There’s alot going on right now; check out the different events in this ‘Events blog’. Aviva ME/CFS! The National ME/FM Action Network’s May 12th Awareness Day for ME/FM submission in the Aviva contest is on the edge of winning $10,000 with the...
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