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 Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) and related chronic complex diseases.
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
Life Before ME / CFS: From Exciting Opportunity to Limited Capacity. My name is Elisabeth. I am 39 years old and became ill with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS) 16 years ago. Since 2018 I have been working as a voluntary translator
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,
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
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
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,
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
BREAKING NEWS We are pleased to announce that we have added a fourth ME / CFS Collaborative Research Center (CRC) to join our End ME / CFS Project. Directed by Alain Moreau, PhD, the ME / CFS Collaborative Research Center at CHU Sainte-Justine/Université de Montréal in
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
“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
Today we’d like to share a story of hope from a Swedish family that has been devastated by ME / CFS. Sanna is a mother of four, and her 14-year old daughter Sara was stricken with ME / CFS in 2018. Since then, Sara
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