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Government and healthcare systems around the world fail to classify myalgic encephalomyelitis (ME) as a serious, complex medical condition, leading to significant neglect in medical care and social services. Diagnoses are often delayed for years, disability qualifications are complicated, and our health care is at risk. ME receives far less funding for research relative to disease burden (only 3-7% of comparable illnesses), despite massive economic costs. Over and over again, people with ME and Long COVID are asked to prove their medical frailty - how sick we really are.
We are the #MillionsMissing. People with ME and Long COVID. And we are Frail and Furious!
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