Category Archives: Myalgic Encephalomyelitis

Unrest on PBS

For those of you who are in the United States, Unrest will be coming to PBS on January 8th. This documentary is a glimpse inside one woman’s journey with Myalgic Encephalomyelitis (ME), a misunderstood, misdiagnosed, pervasive and insidious disease.  It is a love … Continue reading

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Freedom! An ME/CFS Story

Today I bought an electric wheelchair and I’m overwhelmed. How is it possible to feel so many contradictory things at the same time? I cried, laughed, cried some more. The joy I felt, being able to get outside and “go … Continue reading

Posted in ME/CFS, Myalgic Encephalomyelitis | Tagged , , | 9 Comments

#MillionsMissing

Why the hiking shoes you ask. May 25th, 2016 is dedicated to the millions of Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS) patients missing from their careers, schools, social lives and families due to the debilitating symptoms of the disease. ‪#‎MillionsMissing‬ and I … Continue reading

Posted in ME/CFS, Myalgic Encephalomyelitis | Tagged , , | 4 Comments