Equivox guest blog: My life with M.E./C.F.S.

Photo of author and Equivox logo

by Katie, Equivox participant   Hello, my name is Katie, I am 21 years old, and for 4 years I have been living with a condition called Myalgia Encephalomyelitis or Chronic Fatigue Syndrome (M.E./C.F.S.). M.E./C.F.S. is an invisible illness, and its symptoms include, but are not limited to, fatigue, muscle and joint pain, and issues […]

Staff blog: The importance of sharing lived experience

Photo of a sign that says "What's your story?"

by Sam Earle, Project Officer, Equivox  As disabled people,  we know that our specific conditions continually shape our lives in myriad, subtle ways. The effects of disability on our everyday lived experience are too numerous to count, and this is why the bits that we choose to reveal to others are really just the tip […]

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