I have had Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) since March 2002. Both of my sons also got ME/CFS at ages 6 and 10. Our younger son fully recovered after 10 years of mild illness. Our older son still has ME/CFS and also has Lyme disease plus two other tick infections. This blog is about how our family lives with chronic illness, with a focus on improving our conditions and enjoying our lives in spite of these challenges.
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Monday, April 17, 2017
Webinar on Thursday with Top ME/CFS Experts
As part of its ongoing series, Solve ME/CFS initiative is hosting another webinar this Thursday, April 20 at 1:00 pm Eastern Time, featuring two of the top doctors/researchers in ME/CFS in the world: Dr. Joe Montoya and Dr. Susan Levine. They will be talking about recent work and new developments in the ME/CFS research world. Dr. Levine is our own doctor and participates in many research studies, and Dr. Montoya was one of the pioneers of antiviral treatment for ME/CFS (with great success). Both are on the Research Advisory Council at SCMI and are involved with multiple research projects, as well as seeing patients.
I can't wait to hear what they both have to say! The webinar falls squarely into my naptime, but I will watch the video afterwards (and will post a link here). This should be a good one!
You can sign up for the webinar here.
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