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The M.E. and CFS Information Page

Information about ME/CFS, or Myalgic Encephaloyelitis and Chronic Fatigue Syndrome, also called CFIDS.

http://www.cfids-me.org/

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The M.E. and CFS Information Page | cfids-me.org Reviews
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Information about ME/CFS, or Myalgic Encephaloyelitis and Chronic Fatigue Syndrome, also called CFIDS.
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The M.E. and CFS Information Page | cfids-me.org Reviews

https://cfids-me.org

Information about ME/CFS, or Myalgic Encephaloyelitis and Chronic Fatigue Syndrome, also called CFIDS.

INTERNAL PAGES

cfids-me.org cfids-me.org
1

My Story - Mary Schweitzer

http://www.cfids-me.org/mystory10.html

Go to the CFIDS/M.E. Information Page. Mary Schweitzer's Essays on ME/CFS. My History with ME/CFS. Mary M. Schweitzer, Ph.D. Every day was a day survived. To others, I was resting, taking it easy. But not to me. The simplest task took enormous exertion and concentration. The cognitive effort required to go online and meet with my friends tired me out quickly. If I did too much which could be as simple as going out to dinner and sitting upright for an hour the disease slapped me down w...Before I fell ill...

2

CFIDS, M.E., and Chronic Fatigue Syndrome Information Index

http://www.cfids-me.org/links.html

Return to the M.E./CFS Information Home Page. The ME/CFS Information Page. Links to Useful Sources. Definitions of M.E., CFS, and ME/CFS. Good sources of Information on M.E., CFS, and ME/CFS. Specific Research Hypotheses as to the Cause of ME/CFS. What is it like to have ME/CFS? Patient Groups in the United States. Co-Cure ME/CFS and Fibromyalgia "Good Doctor" List (provided by patients. Commercial Testing Labs and Health Supplement Sources. Byron Hyde's Definition of ME/CFS. Are ME. and CFS the Same?

3

CFSAC Recommendations to U.S. DHHS

http://www.cfids-me.org/cfscc/recommend.html

Chronic Fatigue Syndrome Advisory Committee. To the Secretary of the U.S. Department of Health and Human Services. 2 We would urge the DHHS, through the NIH, expedite the issue of an RFA with sufficient set aside funds to attract senior level researchers to engage in the study of CFS. DHHS should fund extramural grants, reviewed by a special emphasis panel knowledgeable in CFS, through RO1, RO3, R21, and Directors Pioneer Award mechanisms. 5 The DHHS should promote, encourage and fund research directed t...

4

Mary Schweitzer's Testimony to CFSAC 9/05

http://www.cfids-me.org/marys/cfsacf05.html

Go to my essays on Living with ME-CFS. Go to the CFIDS/M.E. Information Page. Chronic Fatigue Syndrome Coordinating Committee (CFSCC) of the. US Department of Health and Human Services. September 12, 2005. Mary M. Schweitzer, Ph.D. On July 4, 2005, sometime between 2:30 am when his mother kissed him good night, and 6:30 am when his father came downstairs, Casey Fero died in his sleep. His heart simply stopped. Casey Fero was 23. Pat has had CFS since before Casey was born. She has also been diagnosed...

5

Mary Schweitzer's Testimony Regarding Ampligen to CFSCC 11/99

http://www.cfids-me.org/cfscc/amptestimony.html

Go to my essays on Living with CFS/M.E. and HHV-6a. Go to the CFIDS/M.E. Information Page. Chronic Fatigue Syndrome Coordinating Committee (CFSCC) of the. US Department of Health and Human Services. November 2, 1999. Mary M. Schweitzer, Ph.D. Thank you for the opportunity to speak to you today. On July 12, 1999, 22 weeks into Ampligen treatment, my blood was tested again for the 37kDa and for HHV-6a. The 37kDa was gone, and so was the HHV-6a. Dr. Ablashi recently presented evidence about my c...Several g...

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LINKS TO THIS WEBSITE

quixoticmeblog.blogspot.com 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...

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...

quixoticmeblog.blogspot.com quixoticmeblog.blogspot.com

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...

quixoticmeblog.blogspot.com quixoticmeblog.blogspot.com

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...

circustan.org circustan.org

About

http://www.circustan.org/about

I’m muddling my way through the mercurial medical morass. Of Chronic Fatigue Syndrome, aka CFS, all while trying to keep my humor, health, and happiness. As Hillary Johnson of Osler’s Web. Wryly stated, “calling CFS Chronic Fatigue Syndrome is like calling diabetes Chronic Thirst Syndrome.”. Otherwise known as Chronic Fatigue immune Dysfunction Syndrome. CFIDS), Myalgic Encephalomyelitis. ME), or any clever variant of Post Viral Syndrome, many see the disease (dare it even be called? Follow me on Twitter.

chronicfatigue.livejournal.com chronicfatigue.livejournal.com

chronicfatigue - Profile

http://chronicfatigue.livejournal.com/profile

Created on 6 January 2002 (#431426). Last updated on 9 February 2012. I started this LJ as a sort of online support group for fellow CFS/CFIDSers and their friends, families, and loved ones. This is a very real, and very devastating disease, and i hope that this journal will somehow help all of the people affected. My hope is that this will become a place where we can post our hopes and dreams, as well as our disappointments and frustrations. Hugs, hope, and love*. Http:/ www.co-cure.org/.

immunedysfunction.org immunedysfunction.org

Resources

http://www.immunedysfunction.org/resources.html

Dba: The Vermont CFIDS Association, Inc. a 501(c)3 private foundation. P.O.Box 3162, Burlington, VT 05408 U.S.A. 1-800-296-1445. This illness is to fatigue what a nuclear bomb is to a match. Laura Hillenbrand, author: Seabiscuit and Unbroken. ME/CFS Primer for Clinical Practitioners. Justice for Karina Hansen. A Canary in a Coal Mine. Courtesy of Aljazeera America 1/3/14. Researchers Tie Gulf War Illness. Institute for Neuro Immune Medicine. Let Your Light Shine Through". Treating Chronic Fatigue Syndrome.

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CFIDS - HELP - Úvod

Únava Chronická únava Chronický únavový syndrom Chronický únavový a imunitně dysfunkční syndrom. Designed by Milan Průcha.

cfids-me.org cfids-me.org

The M.E. and CFS Information Page

The ME and CFS Information Page. Ramsay's definition of M.E. My essays on ME/CFS. I have a new blogsite! Check it out - anybody can read the posts; if you want to comment, you have to sign in. My new blogsite is:. XMRV - The Retrovirus behind the misdiagnosis of CFS. In the October 9, 2009, issue of Science. For my best current explanation as a Ph.D. in a social science, a victim of the disease, and a patient advocate, please read my essay on XMRV, XAND, CFS, and M.E. If you to go my blog. I was fortunat...

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FATIGUE, FIBROMYALGIA and AUTOIMMUNE. About Dr. Conley. Free Book and Health Newsletter. Appointment / Contact Us. Or worse yet, you are told it's you, or it's depression, or that nothing is wrong because traditional testing didn't show anything. Our innovative program has allowed over 5,000 people to regain their quality of life. Working together, we will help you get your life back too! There is a tremendous amount of hope! Read more on why you can get better! Read more on CFIDS/FM treatment. Californi...

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CFIDS Meetups - Meetup

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IC.cz

Doména www.cfids.phorum.cz je volná k registraci! Proveďte novou registraci na naší stránce IC. Či pomocí tlačítka níže. Výborný výkon celého hostingu. Nemáte doposud vytvořen žádný web? Založte si nový na IC.cz.

cfidsangel.blogspot.com cfidsangel.blogspot.com

Turtle Medicine: Stories of a CFIDS/Lyme Disease Mom

Turtle Medicine: Stories of a CFIDS/Lyme Disease Mom. About me and this blog. Lyme Resources LOTS to read. Monday, September 22, 2014. Donate a Blog Post This Week For Mesothelioma Awareness Day. 8220;When it comes to a preventable cancer like mesothelioma,. Awareness truly does save lives.”. I found her story more than compelling, but I also admire the idea and the purpose of this campaign. Or, perhaps if you begin on or after Friday, you can compile your favorite MAD articles and blogs and include them...