Esteffiestar suffers from one of the same disorders I do (Fibromyalgia / M.E.) and she was diagnosed the same year I was, so, because I can relate to her, I wanted to share her story to give her support. Sometimes, just showing someone a little love, even in the form of reading their words, is enough to give them a smile for that day. 🙂
M.E. took over my life a little more than five years ago and little by little it’s trying to take over the whole of me.
The 12th of May is Worldwide M.E./CFS awareness day. The week surrounding it its Action for M.E. Week
- Dress up! On May 12th, wear blue for ME/CFS/SEID, dye a strip of your hair blue (when people ask why, tell them it is for ME/CFS/SEID awareness), or just get creative!
http://www.actionforme.org.uk/home
http://solvecfs.org/international-mecfs-and-fibromyalgia-awareness-day-may-12/
I’m coming out about the severity of this illness instead of trying to keep up a social acceptable profile.
That’s what M.E. / C.F.S. / Fibromyalgia awareness day asks of us patients.
Share what it’s like. This is a hard task.
Normally I try to only share the few moments in my life that will get approval and fit in with normal life standards.
But this doesn’t help the cause, getting awareness
is…
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Grits, Hugs, and Sweet Tea 