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If Wishes Were Horses...

     




If Wishes Were Horses...
My personal battle with Chronic Fatigue Immune Dysfunction Syndrome. Although I have worked in the medical profession, I do not claim to be an expert on CFIDS nor do I possess the knowledge and training to decide whether YOU have it. This is a personal description of what I go through, what I deal with, and my experiences as a CFIDS sufferer. My aim is to document my experiences in my attempt to obtain disability, as well as writing as a therapeutic exercise in my journey toward healing. An added bonus, of course, is if I can somehow lend hope and strength to others in my situation. .................................................................................................................................................................................................................................................................



I am a blogger with CFIDS and FM. My blog includes a variety of topics. I save one day just for CFIDS and FM.{;}

CFIDS & ME Bloggers
Welcome To The CFIDS & ME Bloggers Community.{;}This community is for persons with CFIDS/CFS/ME/FM who have blogs.{;}It's also a place to find others like yourselves for support, a shoulder to cry on, to vent, etc...{;}No flaming!!!! If you flame, you are out, plain and simple.{;}Be supportive and show the love to your fellow sufferers.{;}Please write in your blog at least once a week so we know you are ok.{;}Please upload the our logo to your own server.{;}Please specify the url where your community fragment will be placed.{;}Inactive bloggers will be notified. {;}If you are not feeling well , its ok. Just leave a note to let us know how you are doing.{;}If you just wanted another community logo on your site, this isnt the place for you.{;}Active bloggers are also one's who stop by and visit another blogger to say hi, how r ya, are you feeling ok, or welcome to the group.{;}Thats really it. If this sounds good, we will be looking forward to meeting you!