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ME/CFS Blogger Nation
Ring homepage
Ringlink Webring Directory
25 sites out of 37
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My Chemical-Free House
- A guide to building a mould-free, chemical-free house for the MCS and CFS patient.
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Liebjabberings
- Alicia Butcher Ehrhardt's writing blog. I'm a writer - with CFS. I'm blogging my novel Pride's Children, Tuesdays. One main character has CFS, too. I write about living and writing with CFS - and lots of other things.
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4Walls and AView
- 4Walls and AView is an auto-biographical-type blog that chronicles the journey of one who is living with M.E./CFS and FMS. It is a place to be S.I.C.K. by Sharing struggles, Inspiring others, Changing perspectives and passing on Knowledge.
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Alyson's CFIDS Blog
- My life with Chronic Fatigue and Immune Dysfunction Syndrome and Other Chronic Illnesses
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CFS Untied
- Adventures in Illness and Politics
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Dreams at Stake
- A woman's journey of hope through severe ME/CFS
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Falling Fog
- A blog about my battle with CFS/Fibro and myofascial pain syndrome and how its effecting my life and my journey in planning my wedding and trying to concieve or first baby
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Flying through the woods.
- I was diagnosed with ME many moons ago. My health deteriorated to where I lived from my bed, but there has been a discovery. I can now be treated and am improving. This blog gives you my account of my day-to-day life.
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frown at SMILE
- About an unethical study of a training programme called The Lightning Process in children with ME/CFS in UK.
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Hysterical Woman
- Let's stop the hysteria. A blog with a feminist slant on CFS/ME and Fibromyalgia. A mix of current research and personal experiences. by Heide Hayward
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Incy Wincy and M.E.
- my little blog
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Infinite Daze
- I came down with a virus in May 2010 and never got better. This is my illness narrative.
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It's only ME; it's not my mind.
- It's only Myalgic Encephalomyelitis. It's not my mind. Join me for a fun-filled romp with the debilitating disease that's changing my life. Please note, all romping done in slow motion with many rest breaks.
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Life as we know it
- Life with CFS/fibromyalgia -- musings, research, personal experience, calls for action. Knowing the concentration difficulties of CFS patients, most pertinent parts of long posts are highlighted so you can skim rather than reading every word.
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~ME Nytt~
- A Norwegian blog that shares news article, research news, blog-tips and commentaries about ME/CFS.
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No Poster Girl
- Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time.
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Olana's Fog Blog
- My blog started as a record of day to day M.E., a diary in preparation for my appeal tribunal. It has developed to contain general material regarding both M.E. and the medical assessment process.
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Roo's Clues
- Sharing what I've learned about understanding and healing my ME/CFS and my son's autism, which is essentially the same disease.
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Science vs Anti Science
- Life through the lens of an ME Sufferer trying to get research and treatment for this disease
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The Thing With Feathers
- Hanging onto hope for dear life, through 15 years living with & being bedbound from severe Myalgic Encephalomyelitis.
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Thoughts About ME
- Raise profile of ME/CFS so that it can receive the funding and proper attention that has been so long denied. Explore ways to facilitate my ability to communicate with others about, and help them gain understanding of, this disease.
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Twenty Years and Counting
- A blog focused on ME and CFS activism from the perspective of someone who's been sick for twenty years. I have been an on-and-off activist (depending on my health status) for 15 years.
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Verlorene Zeit
- German speaking blog about my life as a severe (bedbound) ME patient with a focus on advocacy.
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We Can Still Blog!
- My life with ME/CFS, and yours.
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X-treme Denial
- XMRV stand for Xenotropic Murine Leukemia Virus Related Virus, has been found to be implicated with prostate cancer and ME/CFS so far. This blog discusses the politic crimes that are still going on, a quarter century after some well known epidemics
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