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THE WHOLE DAMN CHRONIC SITUATION

A life with Chronic Fatigue Syndrome.

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THE WHOLE DAMN CHRONIC SITUATION | thedamnchronicsituation.blogspot.com Reviews
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A life with Chronic Fatigue Syndrome.
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THE WHOLE DAMN CHRONIC SITUATION | thedamnchronicsituation.blogspot.com Reviews

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A life with Chronic Fatigue Syndrome.

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1

THE WHOLE DAMN CHRONIC SITUATION: DAILY LIFE WITH CFS

http://thedamnchronicsituation.blogspot.com/p/daily-life-with-cfs.html

THE WHOLE DAMN CHRONIC SITUATION. A life with Chronic Fatigue Syndrome. DAILY LIFE WITH CFS. WHAT HAVE I TRIED? DAILY LIFE WITH CFS. So day to day, how exactly does Chronic Fatigue Syndrome effect me? I have a nap every day, just 30 minutes before lunch, but it makes a big difference in what I can do. Sometimes I will have another nap around five, if I have a particularly busy day, just to allow me to function. It may sound tedious or irritating or empty to other people, but it is literally the only way ...

2

THE WHOLE DAMN CHRONIC SITUATION: INTROVERSION AND ME/CFS

http://thedamnchronicsituation.blogspot.com/2015/08/introversion-and-mecfs.html

THE WHOLE DAMN CHRONIC SITUATION. A life with Chronic Fatigue Syndrome. DAILY LIFE WITH CFS. WHAT HAVE I TRIED? Friday, August 28, 2015. I read a lot, but it is not often that I come across a book that changes my whole way of looking at my life. I was listening to a TED talk on the TED radio hour. Most people may know what this is, a series of talks by people who are innovators or experts in their field, in all areas of human endeavour and investigation. To actually define this introvert/extrovert dichot...

3

THE WHOLE DAMN CHRONIC SITUATION: BREATHING 2.

http://thedamnchronicsituation.blogspot.com/2015/03/breathing-2.html

THE WHOLE DAMN CHRONIC SITUATION. A life with Chronic Fatigue Syndrome. DAILY LIFE WITH CFS. WHAT HAVE I TRIED? Sunday, March 1, 2015. I've written a lot about the topic of breathing. In the last year or so. It began for me when I was tested in the Breakspear Clinic in. And shown to have a lack of carbon dioxide (CO2) in my system, and a lack of oxygen (O2) getting to my tissues. I have also written about a rebreathing mask. The exercise was very simple, it was all about slowing and deepening my breathin...

4

THE WHOLE DAMN CHRONIC SITUATION: WHAT HAVE I TRIED?

http://thedamnchronicsituation.blogspot.com/p/what-have-i-tried.html

THE WHOLE DAMN CHRONIC SITUATION. A life with Chronic Fatigue Syndrome. DAILY LIFE WITH CFS. WHAT HAVE I TRIED? WHAT HAVE I TRIED? The only things that helped me at all have been Magnesium, the Pantothenic acid (vitamin B5), the B-Complex and the SAM-e, all of which I am still taking. I have taken anti-depressants on a number of occasions, mainly for sleep, at times for depression. I came off the last anti-depressant that I was taking six months ago. The SAM-e is an effective replacement. In my experienc...

5

THE WHOLE DAMN CHRONIC SITUATION: March 2015

http://thedamnchronicsituation.blogspot.com/2015_03_01_archive.html

THE WHOLE DAMN CHRONIC SITUATION. A life with Chronic Fatigue Syndrome. DAILY LIFE WITH CFS. WHAT HAVE I TRIED? Sunday, March 1, 2015. I've written a lot about the topic of breathing. In the last year or so. It began for me when I was tested in the Breakspear Clinic in. And shown to have a lack of carbon dioxide (CO2) in my system, and a lack of oxygen (O2) getting to my tissues. I have also written about a rebreathing mask. The exercise was very simple, it was all about slowing and deepening my breathin...

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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...

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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...

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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...

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Quixotic: My M.E. Blog: Why it's so hard to tell what's causing an ME/CFS crash

http://quixoticmeblog.blogspot.com/2015/05/why-its-so-hard-to-tell-whats-causing.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. Friday, May 15, 2015. Why it's so hard to tell what's causing an ME/CFS crash. I'm not excluding other possible causes of crashes, but those two seem most likely in my case. A normal person who doesn't have ME/CFS might think, "we all know what a cold or flu virus feels like. Can't you tell if you feel like you have a cold or a flu? For many of my...

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Quixotic: My M.E. Blog: My new headache symptoms - another clue

http://quixoticmeblog.blogspot.com/2015/06/my-new-headache-symptoms.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. Monday, June 15, 2015. My new headache symptoms - another clue. I've figured out what this new headache symptom is about. Since my last blog post, in which I wrote about recent headaches, these new headaches have come and gone every five or six days. They usually last about 2 days. Joke if you will about the troglodytic nature of men, but I'd rath...

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Quixotic: My M.E. Blog: 4 Year Anniversary

http://quixoticmeblog.blogspot.com/2015/07/4-year-anniversary.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. Friday, July 10, 2015. Patrick W. Calvin. July 10, 2015 at 2:22 PM. Thanks for sharing.I went through the same thing as the years went by.Its hard to strike the right balance between acceptance and continuing to fight. Best of luck to you! Patrick W. Calvin. August 14, 2015 at 5:09 PM. The Median of Infinity. July 10, 2015 at 5:45 PM. As I see it,...

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Quixotic: My M.E. Blog: Can't Seem to Complete Lyme Provocation Test

http://quixoticmeblog.blogspot.com/2015/06/cant-seem-to-complete-lyme-provocation.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...

quixoticmeblog.blogspot.com quixoticmeblog.blogspot.com

Quixotic: My M.E. Blog: New doctor thinks it's Lyme... I'm not so sure

http://quixoticmeblog.blogspot.com/2015/04/new-doctor-thinks-its-lyme-im-not-so.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. Sunday, April 12, 2015. New doctor thinks it's Lyme. I'm not so sure. Patrick W. Calvin. April 12, 2015 at 11:21 PM. I understand.so called ME/CFS for 30 yrs .NOW, I have found out that I am dealing w/ Lyme.ck out kathleen Dickins work.I am still.trying to understand the whole story .but has opening doors .ck her out. April 10 at 5:17am. Https:/ w...

quixoticmeblog.blogspot.com quixoticmeblog.blogspot.com

Quixotic: My M.E. Blog: January 2015

http://quixoticmeblog.blogspot.com/2015_01_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. Monday, January 12, 2015. 2014 - My Health in Review. Overall, 2014 saw a large return of functionality for me, in ways that just weren't possible a year or two ago. I still have a long way to go, and I realize that the trend could reverse at any time, but for now I'm just trying to enjoy every day in which I don't. Feel like I did a few years ago.

quixoticmeblog.blogspot.com quixoticmeblog.blogspot.com

Quixotic: My M.E. Blog: November 2014

http://quixoticmeblog.blogspot.com/2014_11_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, November 20, 2014. No Interferon for me. I wrote in my October 12th post. Throughout most of October and November, I delayed any decision to start the treatment because the treatment apparently causes severe flu-like symptoms. With my family and work obligations, I couldn't afford to be 100% out of commission with a flu. We've all seen i...

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THE WHOLE DAMN CHRONIC SITUATION. A life with Chronic Fatigue Syndrome. DAILY LIFE WITH CFS. WHAT HAVE I TRIED? Thursday, November 3, 2016. IT HASN'T GONE AWAY, YOU KNOW. In 1995 Adams was speaking at a rally in Belfast. Someone – one of his supporters in the crowd – shouted out a question about the IRA. He kind of smiled, looked out at the crowd and said, in his broad Beyl-fahst accent, “They haven’t gone away, you know”. Https:/ www.youtube.com/watch? These six words became famous, at least in Ireland&...

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