An Engineer with ME / CFS Shares his Story My name is Steve and I’m from Hobart, Tasmania, Australia. I’ve had moderate ME / CFS for around 18 months. I suspect I had a much milder case for much longer. My friends thought I
It’s three weeks into our #MayMomentum campaign. The results to date have been remarkable, and we are so grateful! Your support in May gives us the confidence year-round to forge ahead in uncertain times and the resources to plan for the future
Painting a Hopeful Picture for the Future Today we share a #MayMomentum story from Norwegian artist, Ellen. Ellen’s friend @TheHamOfficial, who is also an artist, recently launched a virtual fundraiser for OMF in honor of Ellen, and the millions of
Spreading Hope One Bear at a Time I have had ME / CFS since I was 16 years old, after having a bad case of the flu. I am now 28. It took me 10 years of searching to finally find a
Breaking News OMF Funded Study: COVID-19 and ME / CFS Against the backdrop of COVID-19, Open Medicine Foundation (OMF) remains focused on finding the answers needed to win the fight against Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) and other chronic, complex diseases. Today,
“ME is not me.” We have no shortage of creativity in our inspiring community, and today we demonstrate this by sharing Olivia’s story, who was diagnosed with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) in 2019. To commemorate last year’s ME / CFS Awareness
The Glue that Binds My name is Melinda and I am an ME / CFS patient, advocate, and OMF Supporter. OMF has made a big impact on my life. A couple of years ago I was able to attend the Community Symposium
BREAKING NEWS We are thrilled to announce actress Jennie Jacques as OMF’s newest Celebrity Ambassador! Jennie is an accomplished English actress known for many TV and movie roles, including Vikings, a popular historical drama television series currently airing on the History channel, where
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
A Life in Stop Motion: A Film Animator & Research Chemist Shares her Battle with ME / CFS My name is Inga and I’m an Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) patient and OMF supporter. The scientific research that OMF conducts and funds
“While Our Bodies Are Weak, Our Spirits Are Strong” My name is April Thompson. I am an Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) sufferer and OMF donor and supporter. I’m also the founder of the Chronic Market, a platform for artists
As someone aware of the impact of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (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
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