Driving research of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS),
Post Treatment Lyme Disease Syndrome (PTLDS), Fibromyalgia and Long Covid

May 22: Embarking on Europe!

Dream. Believe. Do It…Join Team OMF in Hope!

On Tuesday May 22nd Linda Tannenbaum left California with her husband Don to embark on OMF’s End ME / CFS Worldwide Tour European visit and bring hope to patients and their families. OMF’s spectacular Scientific Advisory Board, including three Nobel laureates and renowned scientist Ron Davis as Director, is determined to help unravel the mystery of ME / CFS. As Ben Howell, OMF correspondent on Phoenix Rising, writes on his blog after visiting the Stanford Genome Technology Center: “I left with a message of hope – literally, with Dr. Craig Heller saying, ‘We’re gonna figure this out!’”

Linda will be travelling during the next month through 6 European countries for dozens of presentations to patients, parents and caregivers, including question and answer sessions. She will be giving an OMF research update to present what we are doing to unravel ME / CFS, share hope and encourage our global community to take action and be a part of the solution. In addition, she has scheduled talks with government officials and physicians to raise awareness that ME / CFS is a real, serious disease validated by the United States NIH and CDC.

We encourage you to join Linda at a program nearby: /end-mecfs-worldwide-tour/. If you like to become a sponsor of our Tour, please donate. To find information about our research. Please follow us on Facebook or Twitter. Invite others to sign up for our newsletter.

OMF is committed to open and collaborative research. We look forward to seeing you soon in Europe to exchange hope, ideas and thoughts to conquer this terrible disease, together!

Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) Post Treatment Lyme Disease Syndrome (PTLDS), Fibromyalgia Leading Research. Delivering Hope.Open Medicine Foundation®

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