Scientists gather for ME/CFS symposium this Saturday: Watch online!

Influential scientific researchers in the ME/CFS community will come together this Saturday, Aug. 12 for a one-day community symposium focused on the molecular basis of ME/CFS at Stanford University Palo Alto, California.
Register here to join the livestream and be part of the conversation. View the agenda here. (DVDs can also be ordered for $15 from the Open Medicine Foundation.)
The symposium will be held from 9 a.m. to 5 p.m. PST, (California time). The event follows a two-day meeting of the the world-renowned scientists sponsored by the Open Medicine Foundation.
“To date we have been able to develop a potential diagnostic and treatment screening assay using our new nanofabricated device on a few patients and healthy controls,” wrote Ronald W. Davis, PhD in a welcome letter to the symposium. Davis is director of the Stanford Genome Technology Center and director of the Chronic Fatigue Syndrome Research Center at Stanford University. “We have also generated a large amount of molecular data on a few patients, which has pointed to pathways that should help us understand the disease. Our collaborative team meeting will allow for in-depth scientific discussion of ME/CFS research results, and for strategizing on the best way forward for the scientific community.
“At the Community Symposium, the scientists will update patients and any interested members of the public on our progress towards understanding the molecular basis of ME/CFS and our plans for the future.
Only together can we solve this incredibly complex and horrific disease.”

Facebook
Twitter
WhatsApp
Email

Latest News

#MEAction’s Jaime Seltzer Selected for TIME100 Health 2024

We are thrilled to share with you that Jaime Seltzer, #MEAction’s Scientific Director, has been selected for TIME100 Health 2024, TIME’s new annual list of 100 individuals who most influenced global health this year! This is a huge honor based on years of work fighting for equity for people with ME.  We intimately know the

Read More »
white rectangle with the words: Interview with Author Lauren Saikkonen in black font. There is an image of her book cover, Invisible Illness on the left hand side. And a photo of Lauren on the right hand side. Lauren is wearing a red sweater and is smiling at the camera.

Interview With Lauren Saikkonen – Author of Invisible Illness: Coming of Age, Chronic Illness, and a Mother’s Will to Survive

#MEAction is once again thrilled to share a new book, Invisible Illness: Coming of Age, Chronic Illness, and a Mother’s Will to Survive, with you by author Lauren Saikkonen! This book is an autobiography that covers Lauren’s entire life, but heavily focuses on her battle with Ehlers-Danlos syndrome, ME, and fibromyalgia.  You can purchase this

Read More »
Scroll to Top