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

International Awareness Day 2020

International Awareness Day 2020

Today, OMF is continuing our momentum as we honor International Awareness Day for ME/CFS & FM. We have invited our Social Media Coordinator, Rebecca Handler, to share, in her own words and images, why today means so much to all of us: Today, May 12th, 2020, marks International Awareness Day for ME/CFS and Fibromyalgia. OMF…

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Inga’s #MayMomentum Story

A Life in Stop Motion: A Film Animator & Research Chemist Shares her Battle with ME/CFS My name is Inga and I’m an ME/CFS patient and OMF supporter. The scientific research that OMF conducts and funds is a daily source of hope for me. Their research into the biological dysfunction of various systems in ME/CFS…

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April’s #MayMomentum Story:

 “While Our Bodies Are Weak, Our Spirits Are Strong” My name is April Thompson. I am an ME/CFS sufferer and OMF donor and supporter. I’m also the founder of the Chronic Market, a platform for artists and artisans disabled by the condition ME/CFS to sell their work, share their stories, create awareness about the condition,…

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OMF Funds ME/CFS Treatment Trial

As someone aware of the impact of ME/CFS, you understand, as we do, that there is an urgent need to improve the clinical care for people suffering from this devastating condition. #MayMomentum is all about ensuring that research into ME/CFS and other related chronic, complex diseases leads to results and to life-changing treatments. We hope that…

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#MayMomentum is here!

Today Open Medicine Foundation launches its third annual #MayMomentum, our fundraising campaign in solidarity with May 12th ME/CFS International Awareness Day and dedicated to the millions of lives disrupted by ME/CFS and related chronic complex diseases. We are working to free our community from the cruel restraints of this disease and to shield the millions…

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Giada’s #MayMomentum Story

President of the CFS/ME Italian Association Opens up About her Battle with Illness. My name is Giada Da Ros, I am the president of the CFS/ME Italian Association, as well as a patient myself, and I am part of the newborn EMEC (European ME Coalition). I am an OMF volunteer and this past September I…

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