Share Your Story
For a Chance to be Featured by OMF!
Have you been affected by ME/CFS and related chronic, complex diseases or know a loved one who has? We want to hear from you! Please submit your story to our new Voices of ME web portal for a chance to be featured on our website and social media.
(Patients, caregivers, family members, and friends are all welcome to submit!)
Why does sharing your story matter?
There are many voices of ME/CFS and related multisystem chronic, complex diseases (msCCD). They are scientists, they are artists, they are athletes and more. Before chronic disease, these individuals all lived vibrant, healthy lives. Now, many are forced to abandon their passions as they struggle to find the energy for daily tasks of living. There are no FDA-approved treatments and no cure.
By submitting your story and experience, you’ll be helping us to raise awareness and demonstrate why we must urgently fund research to help millions return to health.
Your voice has undeniable power. Let’s show the world why we must pay attention to ME/CFS and msCCD today.
*Please note not all submissions will be featured.
OMF Named a Top-Rated Nonprofit in 2022!
With the help of our many wonderful supporters, we have been honored with one of the first Top-Rated Awards of 2022 from GreatNonprofits! This is the seventh year in a row that OMF has earned a Top-Rated Nonprofit award.
Thank you for writing reviews to help raise awareness and support our work to end multisystem chronic, complex diseases (msCCD).
“Open Medicine Foundation (OMF) offers open scientific collaboration, expertise, courage, and endurance. This is what ME/CFS patients, including me, have been waiting on for decades. I hope anyone who reads this will support OMF.”
– Libby Boone, Person with ME/CFS
Thank you for being a part of the OMF family! If you are able, please consider donating to our groundbreaking research efforts. Each contribution, of any amount, helps us get closer to our goal of finding treatments and a cure.