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No Poster Girl | Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time.

Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time.

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No Poster Girl | Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time. | nopostergirl.com Reviews
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No Poster Girl | Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time. | nopostergirl.com Reviews

https://nopostergirl.com

Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time.

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shoes | No Poster Girl

https://nopostergirl.com/tag/shoes

Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time. Why I’m No Poster Girl. How My Illness Began. Newly Diagnosed with ME/CFS? Black Dress Day 2014. August 8, 2014. How to accomplish a Black Dress* Day photo for severe ME if you have severe ME yourself and are 98% bedridden (may not be possible for all such folks): Use a morning’s energy to try on three dresses. Pick one … Continue reading →. Drop Me a Line. Join 1,395 other followers. Like me on facebook! Like me on facebook!

2

awareness | No Poster Girl

https://nopostergirl.com/tag/awareness

Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time. Why I’m No Poster Girl. How My Illness Began. Newly Diagnosed with ME/CFS? Black Dress Day 2014. August 8, 2014. How to accomplish a Black Dress* Day photo for severe ME if you have severe ME yourself and are 98% bedridden (may not be possible for all such folks): Use a morning’s energy to try on three dresses. Pick one … Continue reading →. Drop Me a Line. Join 1,395 other followers. Like me on facebook! Like me on facebook!

3

Jocelyn | No Poster Girl

https://nopostergirl.com/author/jocelmeow

Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time. Why I’m No Poster Girl. How My Illness Began. Newly Diagnosed with ME/CFS? I Forgot I Had a Blog. August 24, 2016. That is my favorite fake excuse for abandoning you that I’ve been able to come up with since I last posted here two years ago. The truth, of course, is that much more prosaic and usual reason why you stop … Continue reading →. Black Dress Day 2014. August 8, 2014. The Body and My Body. July 21, 2014. June 6, 2014.

4

To Those Newly Diagnosed With ME/CFS: Four Things I Learned the Hard Way | No Poster Girl

https://nopostergirl.com/2011/11/30/to-the-newly-diagnosed

Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time. Why I’m No Poster Girl. How My Illness Began. Newly Diagnosed with ME/CFS? Chimp Speaks, Part I →. To Those Newly Diagnosed With ME/CFS: Four Things I Learned the Hard Way. November 30, 2011. I hit a nerve with my “Nothing” post about what I did. And mostly what I. Item #1: Stay inside your energy envelope. Here are some of the ways that was said:. People who develop ME/CFS don’t instinctively know that it’s absolut...It’...

5

fashion | No Poster Girl

https://nopostergirl.com/tag/fashion

Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time. Why I’m No Poster Girl. How My Illness Began. Newly Diagnosed with ME/CFS? Black Dress Day 2014. August 8, 2014. How to accomplish a Black Dress* Day photo for severe ME if you have severe ME yourself and are 98% bedridden (may not be possible for all such folks): Use a morning’s energy to try on three dresses. Pick one … Continue reading →. The Lace of Life. March 31, 2014. Drop Me a Line. Join 1,395 other followers. Around wi...

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mecfsselfhelpguru.com mecfsselfhelpguru.com

Resources | ME/CFS Self-Help Guru

http://www.mecfsselfhelpguru.com/resources

Holistic coaching, supporting and empowering people with ME/CFS (S.E.I.D), Fibromyalgia and other chronic illness towards better health, happiness and rediscovered dreams. (Myalgic Encephalomeylitis, Systemic Exertion Intolerance Disease, Chronic Fatigue Syndrome). ME Connect Helpline: 0844 576 5326; email: meconnect@meassociation.org.uk. Membership: 01280 818 968 (or download application form from website). ME Association, 7 Apollo Office Court, Radclive Road, Gawcott, Bucks, MK18 4DF. Tel: 0845 003 9002.

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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.

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Going for an interview in London | iWonderAroundaWorld

https://iwonderaroundaworld.wordpress.com/2007/10/24/going-for-an-interview-in-london

A journey around a world, wondering and wandering. Going for an interview in London. October 24, 2007. Red bus around Russel Square (taken on a day with substantially better weather! I’ve resigned from my current job. For about a week I’m basking in liberated joy of relief and the anticipation of a new chapter in my career. Oh the possibilities! But I am smug. I’ll find work. Jobs will fly in at me. This was one of those Random People Poachers who call themselves recruitment agencies and take your CV and...

thoughtsaboutme.com thoughtsaboutme.com

CFSAC Comments August 2015: Ampligen Price Increase on Shaky Ground | Thoughts About M.E.

https://thoughtsaboutme.com/2015/08/14/cfsac-comments-august-2015-ampligen-update

Thoughts About M.E. Myalgic Encephalomyelitis (M.E.) Advocacy. 267% Price Increase for Ampligen. Oops, they did it again! CFSAC violates FACA →. CFSAC Comments August 2015: Ampligen Price Increase on Shaky Ground. August 14, 2015. I looked into the Ampligen issue–the exorbitant 267% price increase by Hemispherx. CFSAC Meeting August 18. Public Comments by Jeannette Burmeister. Submitted on August 13, 2015. Below are two letters I sent to Dr. Woodcock on August 11, 2015 and today (August 13, 2015) wit...

thoughtsaboutme.com thoughtsaboutme.com

CFS | Thoughts About M.E.

https://thoughtsaboutme.com/tag/cfs

Thoughts About M.E. Myalgic Encephalomyelitis (M.E.) Advocacy. Keep an Eye on Your Walitt: NIH Study Poses Dramatic Risk to Long-Term Disability Benefits. March 21, 2016. Many ME/CFS* sufferers are covered by employer-sponsored long-term disability ( LTD ) policies. These policies almost universally limit LTD benefits to 24 months for disability caused or even just contributed to by a mental/nervous disorder. The following language is taken from a current policy … Continue reading →. February 21, 2016.

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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...

quixoticmeblog.blogspot.com quixoticmeblog.blogspot.com

Quixotic: My M.E. Blog: July 2015

http://quixoticmeblog.blogspot.com/2015_07_01_archive.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, July 23, 2015. I've Cut My Supplements Way Down. In February, I wrote that I wanted to cut my supplements way down. From those that I was most sure were helping, to those that I was least sure were helping. Then I started eliminating supplements from the bottom of the list. Others might wonder: given that I haven't missed the supplements...

quixoticmeblog.blogspot.com quixoticmeblog.blogspot.com

Quixotic: My M.E. Blog: June 2015

http://quixoticmeblog.blogspot.com/2015_06_01_archive.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. Tuesday, June 30, 2015. Can't Seem to Complete Lyme Provocation Test. In a video post from April. We're going way off-label here.). Over the last month or two, I've continued to experiment with fractional doses, hoping that I could find a way to slowly titrate to 20 drops per day. As it stands now, I don't see how I will ever be able to make i...

learningtobalancelifechanges.blogspot.com learningtobalancelifechanges.blogspot.com

Learning to Balance Life Changes: The Liebster Award

http://learningtobalancelifechanges.blogspot.com/2014/02/several-weeks-ago-shelley-from-chronic.html

Learning to Balance Life Changes. What I have learned is I can accomplish many things in baby steps. This keeps life's challenges and chores from being overwhelming, as well as making them more pleasurable. This is why I keep writing and sharing, hoping you will be encouraged to join the dance of balance and grace. WELCOME / ACRONYMS / DISCLAIMER. Saying Bye to Clutter. Living Better with Invisible Illness. Links to Articles About Keeping House. Saturday, February 15, 2014. I started blogging because I d...

cfscentral.com cfscentral.com

CFS Central: HAVE YOU NO SENSE OF DECENCY?

http://www.cfscentral.com/2011/05/next-manhattan-project.html

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Wednesday, May 11, 2011. HAVE YOU NO SENSE OF DECENCY? Here is my testimony at the Chronic Fatigue Syndrome Advisory Committee meeting on Wednesday at Health and Human Services in Washington, D.C. Below the written testimony is the video clip. My name is Mindy Kitei. I’m a science reporter who’s covered ME/CFS for twenty years. Last June, I began my blog, CFS Central, in honor of my friend Nancy Kaiser. Even when the CDC conducted its XMRV study, it stu...

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Life With Severe ME/CFS: A bed-lyin', pill-poppin', muscle-wastin' good time. Why I’m No Poster Girl. How My Illness Began. Newly Diagnosed with ME/CFS? I Forgot I Had a Blog. August 24, 2016. That is my favorite fake excuse for abandoning you that I’ve been able to come up with since I last posted here two years ago. The truth, of course, is that much more prosaic and usual reason why you stop hearing from an ME/CFS blogger I just got too sick to write. Two years later, I have mostly but not entirely re...

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No Post on Sunday

Wednesday, May 12, 2010. It’s not always easy to be creative but even a lull can = something interesting! Love, Post Miss. No post on sunday. Tuesday, May 11, 2010. Love, Post Miss. No post on sunday. Tuesday, May 4, 2010. Tuesday: Get in the game. Love, Post Miss. No post on sunday. Saturday, May 1, 2010. Love, Post Miss. No post on sunday. Thursday, April 29, 2010. Love, Post Miss. No post on sunday. Wednesday, April 28, 2010. Wednesday: Like, whoah. Love, Post Miss. No post on sunday. Love, Post Miss.