For people in US This guide is designed for anyone who is homebound and for people with Myalgic Encephalomyelitis, Chronic Fatigue Syndrome, Lyme...
I didnt see a thread on this but if one exists, could this be merged in? A US medical school, Quinnipiac Medical School, has announced the...
I hope I’m not duplicating a thread - I’ve searched but can’t find anything on this subject. “On April 9, 2019, ME advocates Eileen Holderman and...
[ATTACH] Eric Gordon, MD speaking on the Challenge of Diagnosing the Complex Chronic Patient Dr. Gordon will address the difficulties that...
I got an alert via email a couple days ago requesting folks in the USA to contact their congressional representatives. Signature deadline has...
Here's a relatively easy advocacy action for patients in the USA: Ask your health care professional to watch Unrest online and get continuing...
from Gabby Kleins blog: "A meeting took place on September 11 and 12, 2018 by the ICD-10 Coordination and Maintenance Committee. On September...
From the Unrest website: Watch Unrest and receive CME credit US healthcare providers can now watch Unrest and receive continuing education...
Pa. state Rep. Peter Schweyer speaks on House Resolution 854 designating May 12, 2018, as “Myalgic Encephalomyelitis/Chronic Fatigue Syndrome...
I just saw this from ME Action on twitter (@MEActNet): https://twitter.com/MEActNet/status/930222000966176768 [MEDIA] The statement is in an image...
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