Latest Member Updates
Memories, a Nurtured Neurosis - My sleep was filled with dreams of my dad all night. I miss him terribly. Most days I can shove that grief into a corner and carry on without a second thought, but other days it takes center stage against all other cares in my mind. I still hold onto... - 2012/02/10 All too familiar voice - After three tries, I finally updated my header. The first two were similar but didn't sit well with me, so I chucked them into the cyber wastebasket. I think this one is fitting for the moment. The clapboard signifies how I feel as if though I'm liv... - 2012/02/10 Another Bad Week - "This is H. We're over. Stop calling and texting." I am now single. I slit my wrist. Yes, wrist, as in I failed but who cares. I used H's brand new steak knife. That set of knives costed his rich mom a few hundred bucks. He wasn't there. They weren'... - 2012/02/10 I promise, I'm not dead... - Hello lovelies. Between school, work, and sickness, my blog has fallen by the wayside. Sincerest apologies from me. As far as the weight ordeal, I am gaining for sure. I have been going back and forth between bingeing and starving and have not the fa... - 2012/02/09 Bullet - I am afraid to write of it. I am afraid to speak of it. Because the whisper has only just recently become a voice. And I'm afraid that if I write or speak of it, I will prevent that voice from becoming a roar. I am feeling ol... - 2012/02/09 Alzheimer's Dad pleae vote! - Alzheimer's Dad
follow the link and like on facebook, +1 on google or share with the other button to vote. Right now I'm in 4th place. "Had a Dad" Alzheimer's Blog http://alzheimersdad.blogspot.com
(c) Gevera Bert Piedmont })i({
Thank you for vi... - 2012/02/09
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A sampling from our Member Sites(s) Use the link above to review/visit
My Life With CFIDS & Fibromyalgia
A personal look at living with these devastating life changing diseases.
LymieTees
T-shirts, tote bags, mugs, and more for chronic Lyme Disease sufferers. Try to keep smiling!
Fighting ME
My name is Hannah Butterworth. I live in England. I am 24. I have M.E./CFS and have lived with this illness on and off for the past 13 years. As part of my rehabilitation i have built my own web-site which covers what it's really like to live with a chronic illness, information, my treatment, discussions and my own personal experiences.
Behind The Mirror - The Illness Experience
A personal take on CFIDS, expressed through poetry, essays and prose about what it is like to be severely and chronically ill, by a woman with ME/CFS and Fibromyalgia.
Click here to preview and visit the 4 member sites in
Stories from CFS & Debilitating Diseases Sufferers.
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