Having been diagnosed officially with Chronic Fatigue Syndrome (CFS / ME) in 1992 I have had many times when I have seen no light at the end of the tunnel. This was especially magnified 13 years ago when I also developed severe electro-hypersensitivity (EHS) during pregnancy … [Read more...]
My Vision For A Healthy Future: International ME / CFS / FM / MCS Awareness Day 2015 #May12BlogBomb
On this May 12 - International ME / CFS / FM / MCSD Awareness Day 2015 - I was pondering what to write about. Sally Burch over at Just ME, who is running the #May12BlogBomb, suggested a theme this year could be "A Vision For The Future". I often try to picture my own future … [Read more...]
#ThisIsME Blog Chain – All Post Links – ME / CFS / Fibro Awareness Day 2014
I had the idea of creating a blog chain where people with CFS / ME / FM could share some of the things they usually might not share with people - about themselves personally AND about their lives with CFS / ME / FM, in order to help create awareness of how these illnesses affect … [Read more...]
Day 12: 31 Days To A Better CFS Life – My 5 Fave Ways To Connect With The Online CFS / ME Community
Disconnected and alone. That’s how I felt when I first got really ill with CFS, and even moreso during my pregnancy 12 years ago when I developed the added “bonus” of electrosensitivity. That lost sense of belonging due to CFS is something that can contribute greatly to … [Read more...]
This is M.E. – ME / CFS / Fibro Awareness Day 2014 – Blog Chain
Considering International ME / CFS / Fibro Awareness Day is fast approaching, I thought I'd try to start a blog-chain where we all get a chance to tell the people in our lives a little about how it is to live with CFS/ME – PLUS also let them in on a few other things they may not … [Read more...]