sallyjustme.blogspot.com
Just ME: Well enough to drink coffee?
http://sallyjustme.blogspot.com/2015/05/well-enough.html
ME - Myalgic Encephalomyelitis - not just fatigue. Views expressed are not to be taken as medical advice. 10 Things ME patients need NOW! Tuesday, 12 May 2015. Well enough to drink coffee? Often people find it hard to understand why ME folk can do something once but not repeatedly. I used to think that way too. Before I was ill, I remember hearing a comment about a colleague who was off work on long-term sick leave:. Some-one said, "If he's well enough to be out drinking coffee, he should be back in work!
wolfdreams.wordpress.com
The Deep of the Night | Wolfdreams...
https://wolfdreams.wordpress.com/2015/07/08/the-deep-of-the-night
Life, Spirit, and Health: the View from the Mountain. Laquo; #FWF Kellie Elmore. The Deep of the Night. July 8, 2015 by Ash. Awake, yet again, in the deep of the night,. I listen to the breeze sigh through the forest leaves,. Sounding like the gentle caress of waves on the shore. My ever present companion, Kodi,. Lays watchful at the end of the deck,. As I turn to go sit in my porch swing. A loud snort breaks the silence of the Mountain,. Echoing all around us,. And Kodi is instantly alert and by my side.
cfspatientadvocate.blogspot.com
CFS Patient Advocate: September 2013
http://cfspatientadvocate.blogspot.com/2013_09_01_archive.html
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. My daughter. Survey Results on Adaptogens. When Retreat Means Advance: A Recovered Chronic Fatigue Syndrome/Fibromyalgia Patient Looks Back. OMG: Prof Chalder admits that they made up the death threats themself to ridicule patients. LOOKING AT LYME DISEASE - MSIDS. TICK AWARENESS IN SURREY - LYME DISEASE. Quixotic: My M.E. Blog. Points ...
cfspatientadvocate.blogspot.com
CFS Patient Advocate: August 2013
http://cfspatientadvocate.blogspot.com/2013_08_01_archive.html
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. My daughter. Survey Results on Adaptogens. When Retreat Means Advance: A Recovered Chronic Fatigue Syndrome/Fibromyalgia Patient Looks Back. OMG: Prof Chalder admits that they made up the death threats themself to ridicule patients. LOOKING AT LYME DISEASE - MSIDS. TICK AWARENESS IN SURREY - LYME DISEASE. Quixotic: My M.E. Blog. I have ...
cfspatientadvocate.blogspot.com
CFS Patient Advocate: Hugh and Chris Hempel - and their daughters Addi and Cassi
http://cfspatientadvocate.blogspot.com/2015/02/hugh-and-chris-hempel-and-their.html
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. My daughter. Survey Results on Adaptogens. When Retreat Means Advance: A Recovered Chronic Fatigue Syndrome/Fibromyalgia Patient Looks Back. OMG: Prof Chalder admits that they made up the death threats themself to ridicule patients. LOOKING AT LYME DISEASE - MSIDS. TICK AWARENESS IN SURREY - LYME DISEASE. Quixotic: My M.E. Blog. The Hem...
cfspatientadvocate.blogspot.com
CFS Patient Advocate: October 2013
http://cfspatientadvocate.blogspot.com/2013_10_01_archive.html
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. My daughter. Survey Results on Adaptogens. When Retreat Means Advance: A Recovered Chronic Fatigue Syndrome/Fibromyalgia Patient Looks Back. OMG: Prof Chalder admits that they made up the death threats themself to ridicule patients. LOOKING AT LYME DISEASE - MSIDS. TICK AWARENESS IN SURREY - LYME DISEASE. Quixotic: My M.E. Blog. This is...
cfspatientadvocate.blogspot.com
CFS Patient Advocate: March 2014
http://cfspatientadvocate.blogspot.com/2014_03_01_archive.html
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. My daughter. Survey Results on Adaptogens. When Retreat Means Advance: A Recovered Chronic Fatigue Syndrome/Fibromyalgia Patient Looks Back. OMG: Prof Chalder admits that they made up the death threats themself to ridicule patients. LOOKING AT LYME DISEASE - MSIDS. TICK AWARENESS IN SURREY - LYME DISEASE. Quixotic: My M.E. Blog. In this...
cfspatientadvocate.blogspot.com
CFS Patient Advocate: Dr. Joseph Brewer at ILADS 2013
http://cfspatientadvocate.blogspot.com/2013/10/normal-0-false-false-false-en-us-ja-x.html
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. My daughter. Survey Results on Adaptogens. When Retreat Means Advance: A Recovered Chronic Fatigue Syndrome/Fibromyalgia Patient Looks Back. OMG: Prof Chalder admits that they made up the death threats themself to ridicule patients. LOOKING AT LYME DISEASE - MSIDS. TICK AWARENESS IN SURREY - LYME DISEASE. Quixotic: My M.E. Blog. Dr Brew...
quixoticmeblog.blogspot.com
Quixotic: My M.E. Blog: What I learned from a vacation
http://quixoticmeblog.blogspot.com/2015/05/what-i-learned-from-vacation.html
Tracking my efforts to beat Myalgic Encephalomyelitis (ME), aka CFIDS, aka CFS. Tracking my efforts to beat Myalgic Encephalomyelitis (ME), aka CFIDS, aka CFS. Thursday, May 28, 2015. What I learned from a vacation. In that wake of a recent vacation I took to Croatia, I have to rethink much of what I thought I knew about my illness. Since the beginning of April, I have been in a crash that was severe enough that I wondered if it should actually be called a relapse. I still don't know if it was the massag...
bealightcfsawareness.blogspot.com
Be a light, CFS awareness: this is not a poem.
http://bealightcfsawareness.blogspot.com/2011/09/this-is-not-poem.html
Be a light, CFS awareness. Thoughts, reflections, and facts about Chronic Fatigue Syndrome. Living with CFS: the box story. The Politics of CFS. Words from my tribe. Tuesday, September 27, 2011. This is not a poem. It's been a run on sentence kind of day. A couple of days ago i took a heavy clunk to the head. Which is up there on the list of. Really bad things that should not happen to someone with a neurological disease. I am too sad to write. Maybe it's that life is so damn hard all the time. I wish we...
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