cfswarrior blogspot.com

Three Miles at a Time MECFS Warrior

Three Miles at a Time MECFS Warrior. A blog about my journey with Myalgic Encephalomyelitis and Immune Dysfunction Syndrome including HHV 6, EBV, C. Pneumonia, Bartonella, Postural Orthostatic Tachycardia Syndrome, and Biotoxin Illness. Wednesday, February 11, 2015. Thoughts on the Name Change. Im sure most people have heard by now that the Institute of Medicine IOM committee has proposed changing the name of this disease from Chronic Fatigue Syndrome to Systemic Exertion Intolerance Disease SEID.

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LINKS TO WEB SITE

Ashys Blog Living with M.E.

Another GP appointment and stretching. I have been doing these exercises. I have wondered about contacting the phy.

ChronicallyMe Life with a chronic illness

Some of the information given such as dosage is conflicting. Also important for nerve repair and function. Antioxidant that kills free radicals. For diabetes or bodybuilding may.

Endo en Vogue

Dashed Hopes and Measured Steps. Foxy in the Waiting Room. Even in the Midst of Pain.

Gotlyme Information and resources for lyme disease

Information and resources for lyme disease. One more reason for doing Yoga. The four stages of relapse. Strong Evidence of Lyme Persistence in Monkeys.

Living the CFS Life

Balancing hope and acceptance while living with Chronic Fatigue Syndrome. It is always our conscious choice which secret garden we will tend. Sunday, October 16, 2011. At least it has drawn attention - and research dollars - to our disease. I am grateful for that.

Lyme is Crazy

Saturday, December 31, 2016. Catch Up and A Little Thing Called the Garage. Can you believe that my boys are not small anymore? Monkey is 9 years old and in 3rd grade, Too is 5 years old and in kindergarten. I officially no longer have babies or preschoolers.

Blogging for MECFS Awareness Individuals Blogging For MECFS Awareness Every May

January 31, 2011 by rachelcreative. A lot has changed since and social media has mobilised a lot of people to do their bit. My own personal feelings about What Next .

somewhere i have never travelled

For anyone who has ever believed that a favorite book could be a safe place to go when things get hard. I heart someone with M. Search this blog for books, recipes, etc.

Somewhere I Have Never Travelled Books, Gardening, Art, Life

Books, Gardening, Art, Life. Many things are coming to a close, including this blog. According to the weather man,.

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Three Miles at a Time MECFS Warrior

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Three Miles at a Time MECFS Warrior. A blog about my journey with Myalgic Encephalomyelitis and Immune Dysfunction Syndrome including HHV 6, EBV, C. Pneumonia, Bartonella, Postural Orthostatic Tachycardia Syndrome, and Biotoxin Illness. Wednesday, February 11, 2015. Thoughts on the Name Change. Im sure most people have heard by now that the Institute of Medicine IOM committee has proposed changing the name of this disease from Chronic Fatigue Syndrome to Systemic Exertion Intolerance Disease SEID.

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This web page cfswarrior.blogspot.com states the following, "Three Miles at a Time MECFS Warrior." We saw that the webpage said " A blog about my journey with Myalgic Encephalomyelitis and Immune Dysfunction Syndrome including HHV 6, EBV, C." It also said " Pneumonia, Bartonella, Postural Orthostatic Tachycardia Syndrome, and Biotoxin Illness. Wednesday, February 11, 2015. Thoughts on the Name Change. Im sure most people have heard by now that the Institute of Medicine IOM committee has proposed changing the name of this disease from Chronic Fatigue Syndrome to Systemic Exertion Intolerance Disease SEID."

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