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Three Miles at a Time (ME/CFS Warrior)

Three Miles at a Time (ME/CFS 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. I'm 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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Three Miles at a Time (ME/CFS Warrior) | cfswarrior.blogspot.com Reviews
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Three Miles at a Time (ME/CFS 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. I'm 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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Three Miles at a Time (ME/CFS Warrior) | cfswarrior.blogspot.com Reviews

https://cfswarrior.blogspot.com

Three Miles at a Time (ME/CFS 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. I'm 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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1

Three Miles at a Time (ME/CFS Warrior): January 2015

http://cfswarrior.blogspot.com/2015_01_01_archive.html

Three Miles at a Time (ME/CFS 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. Sunday, January 18, 2015. When first sick I read the book The Alchemy of Illness by Hillary Duff. I actually don't remember much of the book except for one quote which I wrote down and promptly lost with the four subsequent moves that ensued. Likewise, I have come to r...

2

Three Miles at a Time (ME/CFS Warrior): TILT------ing

http://cfswarrior.blogspot.com/2014/12/tilt-ing.html

Three Miles at a Time (ME/CFS 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. Monday, December 29, 2014. TILT- - - ing. Toxin-Induced Loss of Tolerance=TILT=Environmental Illness which seems to be where I'm heading. My reactions are spreading to a wider field of toxins. Things that never bothered me before now bother me. I feel better outdoors&#...

3

Three Miles at a Time (ME/CFS Warrior): October 2013

http://cfswarrior.blogspot.com/2013_10_01_archive.html

Three Miles at a Time (ME/CFS 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, October 30, 2013. I'm going to therapy as well as 12 Step meetings in an attempt to heal how broken the events of the past 6 years have left me. The people that accept that and still continue to call or invite me places are the people I'll ending up being fr...

4

Three Miles at a Time (ME/CFS Warrior): Expectations

http://cfswarrior.blogspot.com/2015/01/expectations.html

Three Miles at a Time (ME/CFS 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. Sunday, January 18, 2015. When first sick I read the book The Alchemy of Illness by Hillary Duff. I actually don't remember much of the book except for one quote which I wrote down and promptly lost with the four subsequent moves that ensued. Likewise, I have come to r...

5

Three Miles at a Time (ME/CFS Warrior): Thoughts on the Name Change

http://cfswarrior.blogspot.com/2015/02/thoughts-on-name-change.html

Three Miles at a Time (ME/CFS 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. I'm 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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Participants | Blogging for ME/CFS Awareness

https://meaware.wordpress.com/participants

What You Can Do. Blogging for ME/CFS Awareness. Individuals Blogging For ME/CFS Awareness Every May. Please lend your support to May 12th – International ME/CFS and FM Awareness Day. Through Facebook or support your local or national ME/CFS or FM organisation in their work. The last active Blogging for ME/CFS was in 2010. For Blogging for ME/CFS Participants 2008-2010. On April 1, 2009 at 8:46 am. ME/CFS Awareness May2009 « RachelCreative. On April 7, 2009 at 2:06 pm. On April 7, 2009 at 5:15 pm. I alway...

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Lyme is Crazy: December 2013

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Tuesday, December 31, 2013. New Year's Eve Ideas for little kids. I'm not much for going out these days. It just takes too much of a toll on my body. Not to mention that my kids are really small (ages 2 and 6), so we're usually in bed WAY before the midnight bell rings. So, I've put together some ideas that we can do this year, together, as a family. 3 Sparkling Cider. To let the kids have a taste of celebration we'll toast with sparkling cider. Labels: Happy New Year. Subscribe to: Posts (Atom). Amy Tan...

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Lyme is Crazy: New Year's Eve Ideas for little kids

http://lymeiscrazy.blogspot.com/2013/12/new-years-eve-ideas-for-little-kids.html

Tuesday, December 31, 2013. New Year's Eve Ideas for little kids. I'm not much for going out these days. It just takes too much of a toll on my body. Not to mention that my kids are really small (ages 2 and 6), so we're usually in bed WAY before the midnight bell rings. So, I've put together some ideas that we can do this year, together, as a family. 3 Sparkling Cider. To let the kids have a taste of celebration we'll toast with sparkling cider. Labels: Happy New Year. Subscribe to: Post Comments (Atom).

lymeiscrazy.blogspot.com lymeiscrazy.blogspot.com

Lyme is Crazy: Summer's Over Already?

http://lymeiscrazy.blogspot.com/2013/08/summers-over-already.html

Friday, August 23, 2013. I'm not really sure where the time has gone, but Monkey started Kindergarten on Monday - wow! Roo was not very happy about it, to say the least! But we did get away the week before school started for an unplugged vacation in the mountains! Luckily, this big one didn't get away! We played puzzles, pine cone golf, and climbed rocks. Found a local playground. Ate lots of meals outside:. And just generally got dirty! Labels: back to school. August 24, 2013 at 12:41 PM. Where I grew up.

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Lyme is Crazy: February 2013

http://lymeiscrazy.blogspot.com/2013_02_01_archive.html

Thursday, February 28, 2013. DIY project #1 - dishwasher detergent. A few years ago we decided to go non-toxic with all our cleaning supplies and our grocery bill skyrocketed! Buying the name brands is expensive! So in efforts to tame our budget a little bit I decided to try my hand at making some cleaning staples. First up (mainly because that's what we were out of) was Dishwasher Detergent. Super simple and works well, too. Here's what I did:. 1 cup washing soda ( you can make your own from baking soda.

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Lyme is Crazy: December 2012

http://lymeiscrazy.blogspot.com/2012_12_01_archive.html

Monday, December 24, 2012. Christmas through the eyes of a 5 year old. And they sent their disciples to him, along with the Herodians, saying, “Teacher, we know that you are true and teach the way of God truthfully, and you do not care about anyone’s opinion, for you are not swayed by appearances. Sunday, December 23, 2012. I've been absent from the blogosphere lately because I've been treading water and almost drowning! It's a good thing I love them all so much or I think I'd just give up. Being Chronic...

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Lyme is Crazy: May 2014

http://lymeiscrazy.blogspot.com/2014_05_01_archive.html

Friday, May 9, 2014. Semi-Permanent Rinse and Repeat. I don't know how to even start this post. Like everything in my brain lately, I know what I want to say but not quite sure how to say it. As such, I've thought many times about just closing up my blog and moving on, but then I'll think of something worthwhile to post . only to struggle to put the words to paper. Subscribe to: Posts (Atom). View my complete profile. Where I grew up. Where I live now. Semi-Permanent Rinse and Repeat. Living the Lyme Life.

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somewhere i have never travelled: Moving! (new blog address)

http://never-travelled.blogspot.com/2010/04/moving.html

For anyone who has ever believed that a favorite book could be a safe place to go when things get hard." - Neil Gaiman. I read, cook, make art and try to figure out what the heck I'm supposed to be doing with my life. I chronicle it here. You can contact me at daphneannphillips(at)gmail(dot)com. If you'd like some design work, please contact me at www.daphnephillipsdesign.com. View my complete profile. Follow me on Twitter. I heart someone with M.E./CFS. Search this blog for books, recipes, etc.

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CFS Ramblings: Mental Fatigue caused by decreased parasympathetic activity

http://ramblingsearcher.blogspot.com/2011/10/mental-fatigue-caused-by-decreased.html

My experiences trying to heal from ME/CFS with a lot of pseudo-science thrown in for fun. Tuesday, October 25, 2011. Mental Fatigue caused by decreased parasympathetic activity. I really think the explanation at http:/ www.behavioralandbrainfunctions.com/content/7/1/17/abstract. Is what I have been looking for! Thanks to dinet for this link. Labels: dysautonomia mental SNS ANS. Subscribe to: Post Comments (Atom). Histamine Intolerance- contributor to symptom spectrum? Mast cells and CFS symptoms.

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Three Miles at a Time (ME/CFS Warrior)

Three Miles at a Time (ME/CFS 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. I'm 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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