The story of OMF supporter Martin Den Hollander, a musician living with severe ME/CFS. Despite his health battle, he continues to use his music as a force to help those living with ME/CFS.
The View for ME Project August 2021 In recognition of Severe ME Awareness Day on August 8, 2021, Open Medicine Foundation (OMF) is taking this month to share stories from people living with severe Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) to
OMF Ambassador Jacqueline Ko celebrates her birthday with a fundraiser for research: Donate before August 1 for the chance to have your gift tripled! In celebration of her 30th birthday, multi-award-winning opera singer and OMF Ambassador Jacqueline Ko, kicked off
OMF is inspired and moved by the creativity and resilience of our community. Throughout 2021, Kristine Oma, dancer, choreographer, and person with ME/CFS, has been creating digital dance performances to benefit ME/CFS research.
Thank you for your support during #MayMomentum! Thanks to our community’s generosity and shared dedication, our fourth annual May Momentum campaign was a huge success. Through individual donations and personal fundraisers on Facebook, Instagram, Twitch and other platforms, we raised
In 2017, Rebecca’s life was turned upside down when she came down with an illness that prevented her from leaving her bed and going to work. Soon after, she was diagnosed with ME/CFS. Over the next six months, Rebecca found herself completely confined to bed, sleeping up to 36 hours at a stretch.
Last chance to join the momentum: Support ME/CFS research today! This is the LAST chance for you to support Open Medicine Foundation’s #MayMomentum campaign! All proceeds help advance critically needed research of chronic, complex illnesses. Since our inception, donors from around the
Last day to give to #MayMomentum! There’s still time to make an impact and accelerate research around the globe — donate to OMF’s May Momentum campaign today! All gifts of any amount support urgent biomedical research to find treatments and
With your support, Open Medicine Foundation funds open, collaborative research so that, as soon as possible, precise diagnostic tools and life-changing treatments can be available to people with ME/CFS and related chronic, complex diseases such as Post-Treatment Lyme Disease Syndrome, Fibromyalgia, and Post-COVID Syndrome.
A #MayMomentum spotlight! New Interview with OMF Ambassador Jacqueline Ko!
Multi-award-winning opera singer and Canadian Open Medicine Foundation Ambassador Jacqueline Ko, long known for her critically acclaimed stage performances, is a proud supporter of OMF’s May Momentum campaign.
When Linda Tannenbaum’s 16-year-old daughter came down with sudden onset ME/CFS in 2006, she was shocked to discover that there were no diagnostic tests or treatments for the devastating disease — one that prevented her daughter from leaving her bed and
#MayMomentum research news! Transforming the diagnosis of chronic complex diseases: An update on the PASS/CAT project You might remember last year OMF announced that we are working on an exciting new project to streamline the arduous diagnostic process for people
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