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All Comments (2)
Sharonader 1 year ago
I've been diagnosed twice, once in Canada & here in the US, 10 yrs apart. If people only knew what it was like to suffer with this every single day of your life...
I am so happy that it seems to be getting more info out lately and hopefully more and more people will see this as real, and not "in your head"!
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Melissa Daniels 1 year ago
wearing purple for myself, diagnosed just last year and it's devastated my quality of life. No one can understand the pain we go through fighting this invisible illness. The pain, the fibro fog, the loss of balance and resulting concussions or in my case repeated injuries to my poor right foot baby toe. Love the video
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