Driving research of Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS),
Post Treatment Lyme Disease Syndrome (PTLDS), Fibromyalgia and Long Covid

Category: Voices

Jody’s ME/CFS Story

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

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Leah’s ME/CFS Story

“I was a 20-year-old enjoying adventures. Then I developed an infection that changed my life.” Leah shares her experience living with ME/CFS and related chronic, complex diseases.”

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April’s ME/CFS Story

April’s ME/CFS Story:“Our Bodies May Be Weak, But Our Spirits are Strong” My name is April Thompson. I am an ME/CFS sufferer and OMF donor and supporter. I’m

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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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