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My MS and Me

My MS and Me

 

Carolyn Hinds 

 

I’m not sure where or how I should start this essay. As I sit in bed with my laptop resting on the special cushion I use for it on my legs, I’m filled with a multitude of emotions and physical sensations. 

Emotionally, I’m nervous about how vulnerable I want to be sharing my experiences as a chronically ill disabled Black woman living with Relapse-remitting Multiple Sclerosis (RRMS,

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Originally published as My MS and Me at The Disability Visibility Project

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