Erica’s Story: Redefining Life with ME/CFS
Living with ME/CFS is not only debilitating, but life-altering. This is especially true for a young adult planning for a normal future. It has been
TRIPLE YOUR IMPACT during Triple Giving November | All Donations to OMF are TRIPLED through December 3
Living with ME/CFS is not only debilitating, but life-altering. This is especially true for a young adult planning for a normal future. It has been
Today, we are privileged to bring you the narrative of extraordinary courage, resilience, and strength. At just 14 years old, Charlotte’s life took an unexpected
My name is John. I was a career firefighter/paramedic who was exposed to a person with COVID at work in December 2020 before vaccines were
I was a sophomore in college and living life to the fullest. I was extremely active, and that year alone, I ran two half marathons and one full. December 31st, 2012, I woke up feeling like I was coming down with a bad flu.
Jody’s ME/CFS Story My name is Jody Keeler. On February 26, 2011, my life changed when I came down with pneumonia and never recovered. Before
Myalgic Encephalomyelitis & COVID Long-HaulersBy Kim Eggers I am strong. You’re not going to hear many people say that. They’re bragging; they’re over-confident, and no
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