What do you do if you have a disease which has few clinical trials but lots of patients needing help, and 30 or so practitioners with decades of experience under their belts?
Instead of waiting for a clinical trial to get underway (or not) you ‘tap their intuition’; i.e. you design a survey designed to detect what they think works in ME/CFS.
That’s what the The CFIDS Association (whoops) – Solve ME/CFS Foundation – did. They invited about 30 ME/CFS experts (Dr’s Jose Montoya, Øystein Fluge, Katherine Rowe, Carl-Gerhard Gottfries, Nancy Klimas, Peter Rowe, Italo Biaggioni plus about 20 more) to tell them how. Fifteen ended up telling them:
- How effective the drugs they used were
- What kind of alternative treatments worked
- How they strategized their treatment approaches; i.e., which symptoms did they treat first? Which symptoms were related?
The results are coming soon. Find out more here.
Make sure you don’t miss another one by registering for our free ME/CFS and Fibromyalgia blogs here...
Tell us how your coronavirus vaccination went and find out how other people with ME/CFS and/or FM fared with their coronavirus vaccination in Health Rising’s Coronavirus Vaccine Side Effects Poll.