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.
Friday, September 27, 2019
Webinar: Advances in ME/CFS Research and Clinical Care
Solve ME/CFS Initiative has an awesome on-going series of webinars on a wide range of topics for ME/CFS patients and their doctors, and the one scheduled for next week sounds especially good:
Dr. Kenneth Friedman will be hosting a webinar on Thursday, October 3, 2019, on Advances in ME/CFS Research and Clinical Care, starting at 10 am Pacific Time and 1 pm Eastern Time. You can read all the details about the webinar here. And you can register for the webinar here.
I'd really like to catch this one, but they are always scheduled during my nap time! Luckily, Solve ME/CFS posts videos of past webinars on this page - topics include genetics, brain inflammation, school accommodations, the disability process, and more. What a wealth of knowledge! That same link also describes upcoming webinars, so you can plan ahead.
I'll have to watch this one after it airs, but maybe you can catch it live - sign up today! It's free and sounds like it will be very informative.
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