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Living With Chronic Fatigue Syndrome Just another WordPress.com weblog

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LINKS TO WEBSITE

CFS Patient Advocate

The job of Patient Advocate came upon me uninvited. I did not apply for this job, nor did I have any qualifications for it. I am a sculptor, not a doctor or a researcher. LOOKING AT LYME DISEASE - MSIDS. BREAKTHROUGH IN FRANCE FOR TREATING CHRONIC LYME PATIENTS.

Tools, Treatments Techniques CFSME Lyme Recovery Path

Each person did it their own way with their own sense of determination and grace. Hopefully you will find yourself on this list one day soon. My patient experience with Dr.

Chronic Fatigue Syndrome and M.E. Information about ME CFS

An interesting and informative article from the Living With Chronic Fatigue Syndrome Blog. The article also points out. 8221; I am not a doctor and patients should consult with their healthcare professional before undertaking any treatment regime. For the full article click here. Why Am I So Tired? Nortripty.

Dreams at Stake

Sunday, January 29, 2017. I love to travel and experience new things. I am restless and, in my healthy days, I thrived on change. I am somewhat claustrophobic and hate being in small, confined spaces .

eaubleue mecfs musings A Belgian blog on MECFS

The urge to write it all down has slowly crept in on me over the course of the last 6 months. Hardly noticeable at first, just occasionally lurking from its hiding place in my memory and consciousness. Then, gradually, the idea started nibbling its way to the surface. Today it has evolved into a necessity. Infection, or mononucleosis, or Pfe.

THE NICEGUIDELINES BLOG

Doctor Speedy and ME in search of medical honesty. Sunday, September 24, 2017. Please SMILE and GETSET for the FUQOFF trial. Thursday, June 29, 2017. Tuesday, June 27, 2017.

Sopravvivere alla sindrome da fatica cronica

Sopravvivere alla sindrome da fatica cronica.

Failure to Thrive

A CFS patient feels the same or worse than congestive heart failure. The same or worse than late stage AIDS. A CFS patient feels every day significantly the same as an AIDS patient feels two months before death. Dr Mark Loveless, AIDS and CFS researcher, in a statement to congress on CFS Awareness day, May 12th, 1995. Sunday, October 31, 2010. We are still in t.

masked CANARY From a Yellow Canary of the 21st century, living in our disabling biosphere

Facebook Groups for MCSers and Family. Fergiemoto, the Shy Creative One. From the Land Down Under. Jill, the Science Journalist. Michael Durant of Wales, UK. More Canaries Tell Their Story. Sharon, How Sick is Sick? Talking about Perfume at Work.

kraftycatcreations Jewelry Designed Crafted With Your Unique Style In Mind

Jewelry Designed and Crafted With Your Unique Style In Mind. Enter your email address to follow this blog and receive notifications of new posts by email. Luna, the Little Chomper. Letters From A Spectrum mom. My Mind in a Book. Seeking a Life Full of Laughter. Published on Jul 21, 2015. ME Where Are We? A question I would like a great answer to.

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PARSED CONTENT

The site had the following in the homepage, "September 13, 2017 by cfssufferer." I noticed that the web site stated " Mestinon, AKA Pyridostigmine, is an acetylcholinesterase inhibitor typically used to treat myasthenia gravis- a neuromuscular disease." They also stated " It is a drug that can markedly reduce fatigue and enable patients to exercise in general disorders. Has included Mestinon in a list encompassing his favourite drugs for ME patients."

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Living with Polyneuropathy CIDP, GBS, CMT

Check the Help tab above. Since site content and usernames are google searchable, please protect your anonymity by creating a unique username. All of the material provided on this site is for informational purposes only and is not a substitute for professional medical advice or treatment.

Living With CLIPPERS

A blog about the experience of living with CLIPPERS - Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids. Sunday, 21 January 2018. A reminder of warmer times.

Living With CML

We will all learn to live with this illness, Chronic Myelogenous Leukemia, that is in one of us. I hope to share the journey with others and to make a difference along the way. Tuesday, March 06, 2018. And then I found a couple of groups online filled with others with CML. At first I thought it was a typo when I read that some had been alive, and going strong, 10 and 12 years after diagnosis! I am more than happy, more than utterly grateful. And so I find myself in a very happy place.

! Living with Ulcerative Colitis

Monday, September 20, 2010. Just get out there and do it. Thursday, September 16, 2010. Many people think that networking is something that you do, rather than a way that you live. Networking is a life skill, rather than something you do only when you want something. Tuesday, September 14, 2010.