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Ffion’s #MayMomentum Story

It’s a Small World I have a degree in English and French. I love languages, literature, writing, art, nature, and card-making!  Before ME / CFS and Fibromyalgia hit following a viral infection in 2007, I also loved opera, film, theatre, concerts, walking,

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Anton & Holger’s #MayMomentum Story

The Gift of Hope Today we’d like to share a #MayMomentum story of hope, resilience, & philanthropy from Swedish OMF supporter Anton. This March, Anton created a Facebook fundraiser for OMF in honor of his brother Holger’s 35th birthday, who

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Kyle’s #MayMomentum Story

The Space Between Zero and One The first time I heard about Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) and OMF was about a month or so into dating my current girlfriend of 2 years. I had heard about ME / CFS previously from

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Cecilia’s #MayMomentum Story

My name is Cecilia Ekhem and I live outside the town of Sundsvall in Sweden with my husband and one child at home, and one adult child. I am unfortunately very tightly connected to Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS). Rather,

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“My Long Walk for ME”: A Team OMF Spotlight

Today we’d like to spotlight Magnus Svensson, an exceptional Team OMF member from Sweden. A few years back, Magnus’s wife was diagnosed with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS). He decided to swiftly take action by creating a Team OMF fundraiser

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The Research Continues at Open Medicine Foundation

In a world seemingly upended, Open Medicine Foundation can offer you the assurance that this crisis will not divert us from our search for a cure for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS). I thought I would take a moment to

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Ron Davis Update

“We are doing everything we can to continue progress on Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) during this time when we can’t go into the lab. This is a photo of me on a zoom conference call with doctors and researchers

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March 2020 Newsletter

OMF 2019 YEAR IN REVIEW We realize that you take your philanthropy seriously, and we are honored by your belief in our mission and our efforts to end Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS). The accomplishments contained in the following, OMF

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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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