Awareness for me turning into M.E.

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. 🙂

Steffi's Babylonian Sweet Peas

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…

View original post 1,528 more words

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