There is currently an anonymous survey for CFS patients to take where the data received will be used in a future article to educate the public about CFS.
The article will be written by Dorothy Wall (author of Encounters with the Invisible: Unseen Illness, Controversy, and Chronic Fatigue Syndrome) and Dr. Lily Chu, MD, MPH – both women diagnosed with ME/CFS. Their goal is to then publish the results in a large-circulation consumer magazine and they are interested in the experiences of older patients compared with those of younger individuals.
I am unable to provide a direct link to the survey because I already took it so my computer won’t let me go back to that screen, but if you click on the link below it will take you to the page where you can get to the survey.
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