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Ashy's Blog | Living with M.E.Living with M.E.
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Living with M.E.
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Living with M.E.
Summer fun and back to the old routines (maybe) | Ashy's Blog
https://ashy00.wordpress.com/2011/09/15/summer-fun-and-back-to-the-old-routines-maybe
Living with M.E. Summer fun and back to the old routines (maybe). September 15, 2011 in art. I have had a pretty good summer! So here I am back at home and contemplating what I want to focus on over the next few months. Some things have come out of the GP appointment which will take some time and focus. I will talk about them in another post. So I need to make time and space for that. I am quite excited about it! I subscribe to Sustainably Creative, by Michael Nobbs. Blogging for ME Awareness. September ...
Another GP appointment and stretching | Ashy's Blog
https://ashy00.wordpress.com/2011/12/20/another-gp-appointment-and-stretching
Living with M.E. Another GP appointment and stretching. December 20, 2011 in cfs/me. I am very late in blogging about my last GP appointment, as things have been very busy here and I have just not had chance. It was months ago but I do want to just say that she was excellent again and confirmed to me that even little gentle stretches that are not held long are beneficial and to just give it a try. I have been doing these exercises. Blogging for ME Awareness. From Fatigued To Fantastic. ME/CFS blogs (& re...
Best GP Appointment! | Ashy's Blog
https://ashy00.wordpress.com/2011/09/15/best-gp-appointment
Living with M.E. September 15, 2011 in health. I had a really great appointment with my GP last week. I have only been seeing her for a short while so we are still getting to know each other, and it was great to feel that my hunch that she is really great seems to be ringing true. Has anyone tried Clonazepam and do you take it in the day for muscle tension/pain or sensory overload/neurological symptoms? I have started taking it at night and sleep better but my symptoms remain…). Blogging for ME Awareness.
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About | Aces Full
https://acesfull.wordpress.com/about
Notes on micro stakes poker. I’m blogging my progress (and occasionally lack of progress) in micro stakes poker mainly to create a record of the mistakes I’ve made and a reference point for the future, so I can see what I’ve learned. Writing down a learning process like this helps me to progress by giving me the opportunity to review what I’ve done and identify development needs. My objectives are:. Develop links with other players and sites. Keep a record of progress. Leave a Reply Cancel reply.
L'Ombre de mon Ombre: Look ! I'm in a band
http://lombredemonombre.blogspot.com/2013/11/look-im-in-band.html
Saturday, November 02, 2013. I'm in a band. Many many moons ago, my dear chum Lee Lee Ingram. And I were saying how much we missed being creative and how much this illness gets in the way. Ever one to grasp the nettle (! The fabulous Miss Mitsi B painted the cover art for us and she also features in the video which she produced for us. Http:/ www.youtube.com/watch? To see more of Mitsi's great artwork go to her website here - http:/ www.mitsib.com. This is so freaking exciting! Seriously though, Im super...
L'Ombre de mon Ombre: November 2012
http://lombredemonombre.blogspot.com/2012_11_01_archive.html
Friday, November 23, 2012. 23rd November 2012 : a special day and a special anniversary. Today is the 23rd November. For some reason, this date has featured more than most in my life. 23rd November was the day my Grandmother was buried. More recently 23rd November was the day my dear dog died last year. 23rd November was the day I heard that my Benefits would stop because I had been found fit to work and would have to Appeal or find a way of earning a living. You can read the full story here. Recommend a...
Living the CFS Life: New Post
http://livingthecfslife.blogspot.com/2010/02/new-post.html
CLICK HERE FOR BLOGGER TEMPLATES. Living the CFS Life. I have had CFS since 2006. It has taken me awhile to find acceptance of this debilitating disease. I've finally come to realize that life with CFS means less doing and more becoming. I'm rebuilding who I am and what my dreams are. I am living the CFS life. Friday, February 12, 2010. I have a new post on my new blog: http:/ living-the-cfs-life.blogspot.com/. Oh, should I link directly to your new blog instead of this one? February 14, 2010 at 10:56 AM.
Living the CFS Life: May 2009
http://livingthecfslife.blogspot.com/2009_05_01_archive.html
CLICK HERE FOR BLOGGER TEMPLATES. Living the CFS Life. I have had CFS since 2006. It has taken me awhile to find acceptance of this debilitating disease. I've finally come to realize that life with CFS means less doing and more becoming. I'm rebuilding who I am and what my dreams are. I am living the CFS life. Thursday, May 28, 2009. Could This Be Possible? Dr Kenny De Meirleir announced today that he has unlocked the mystery of ME/CFS. Http:/ www.prohealth.com/library/showarticle.cfm? Labels: a good day.
Living the CFS Life: October 2009
http://livingthecfslife.blogspot.com/2009_10_01_archive.html
CLICK HERE FOR BLOGGER TEMPLATES. Living the CFS Life. I have had CFS since 2006. It has taken me awhile to find acceptance of this debilitating disease. I've finally come to realize that life with CFS means less doing and more becoming. I'm rebuilding who I am and what my dreams are. I am living the CFS life. Tuesday, October 27, 2009. People's Health Blogger Awards. Sue was always there to open my eyes and show me different paths to understanding just what was going on with me. It was from her that...
Living the CFS Life: March 2009
http://livingthecfslife.blogspot.com/2009_03_01_archive.html
CLICK HERE FOR BLOGGER TEMPLATES. Living the CFS Life. I have had CFS since 2006. It has taken me awhile to find acceptance of this debilitating disease. I've finally come to realize that life with CFS means less doing and more becoming. I'm rebuilding who I am and what my dreams are. I am living the CFS life. Tuesday, March 31, 2009. I have two opposing symptoms that love to drive me nuts! First of all, I'm sensitive to cold, and I feel cold ALL the time! Is this why I never feel rested? Sometimes, I wa...
Living the CFS Life: December 2009
http://livingthecfslife.blogspot.com/2009_12_01_archive.html
CLICK HERE FOR BLOGGER TEMPLATES. Living the CFS Life. I have had CFS since 2006. It has taken me awhile to find acceptance of this debilitating disease. I've finally come to realize that life with CFS means less doing and more becoming. I'm rebuilding who I am and what my dreams are. I am living the CFS life. Friday, December 11, 2009. Cake Wrecks and Charitable Donations. The wonderful people at Cake Wrecks. Http:/ cakewrecks.blogspot.com/2009/12/catchin-spirit.html. Monday, December 7, 2009. Third, th...
Living the CFS Life: Past Fear and Frustration
http://livingthecfslife.blogspot.com/2010/02/past-fear-and-frustration.html
CLICK HERE FOR BLOGGER TEMPLATES. Living the CFS Life. I have had CFS since 2006. It has taken me awhile to find acceptance of this debilitating disease. I've finally come to realize that life with CFS means less doing and more becoming. I'm rebuilding who I am and what my dreams are. I am living the CFS life. Thursday, February 4, 2010. Past Fear and Frustration. I'm not happy with my many negative posts lately, but I understand where they are coming from. Thanks to Renee's recent post, I am now coming ...
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ashy in a sentence | simple examples
In A Sentence .org. The best little site that helps you understand word usage with examples. Ashy in a sentence. Wall has gone from being a self-described ashy kid with cornrows who sold candy from his backpack in middle school to living the sweet life. Now, I really get a huge giggle out of the ashy grill picture- its exceptionally difficult to find a SINGLE piece of food on the actual grate. Lofty monuments, slender steeples emerged from the gloom; a kind of ashy light was spread abroad. Explosive erup...
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Ashy & Family
My Daughter and Special Little Angel! Ashley and Seth Thomas. A Precious Little Angel!
Ashy's Blog | Living with M.E.
Living with M.E. December 20, 2011 in cfs/me. I find I am spending a lot of time on facebook talking to other people with ME and other chronic health problems and that has replaced blogging a bit for me, despite having met most of them via my blog! Perhaps it has served it’s purpose…. Anyway, thanks for reading this far and Happy Solstice, Season’s Greetings etc. Another GP appointment and stretching. December 20, 2011 in cfs/me. I have been doing these exercises. I have wondered about contacting the phy...
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the Rat
Sunday, October 25, 2009. Back in the day. Some stupid story I wrote in grade 6 -. Once upon a time in a sleepy place called Misia, there were two best friends called Bill the alligator and Tim the monkey. Tim lived on a plum tree on the bank of the. The tree had the sweetest fruit in the entire region. The tree was more then a thousand years old and the owners of that tree were Tim the monkey and Bob the dodo. 8216;Yes, that’s what we want, sweat meat.’. 8216;That’s your problem, I suggest that yo...
ashy1012 - DeviantArt
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