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ChronicFatiguesupport.com

01-31-2007

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   ProHealth CFS HealthWatch

Treatment & Research News
January 31, 2007
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OUR MISSION
"To empower patients to take control of their health by providing current research and treatment information, quality health products, community, and advocacy."
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$2.5 Million Raised and Donated to Research. more

This Week's Highlights
 
· Pat Fero's IACFS conference news

· Elimination diet for CFS patients

· Q&A on infection & CFS

· Marshall Protocol patient's update


· Trials of 'naturals' in depression
  & duloxetine trial for CFS fatigue


· Abstracts of non-drug studies; more

· Readers' comments & questions

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Founder's Corner
Rich Carson

Advisory Board Proposes New Name for CFS!

Today - January 31, 2007 - is a landmark for 'Chronic Fatigue Syndrome' patients and our Campaign For A Fair Name.

I could not be more pleased to announce that the eight members of the CFS Name Change Advisory Board of experts have reached consensus on a suggested new name for this disease - and at their recommendation ProHealth will submit their proposal to the community. Because of the gravity and timeliness of this landmark decision, we will send you a special, separate e-mail informing you of their finding. So please look for it in your e-mail inbox within the next few days.

These dedicated scientists have taken their responsibility in the campaign very seriously, and their commitment to CFS patients is unwavering. Though a period of comment, debate, and planning is sure to follow, I know you will join me in extending them our sincere thanks for their extraordinary efforts. And thank you for your patience and support.

Your fellow advocate for justice in finding an appropriate name for CFS,

Rich Carson

CFS Patient and ProHealth Founder

Please rate this Founder's Corner


Features

An Informal IACFS Conference Summary from Wisconsin's Pat Fero

Here's a "broad brush" summary of research and treatment highlights from the 2007 IACFS conference, by Pat Fero - Executive Director of the Wisconsin CFS Association. As she notes it's dedication, not glory, that motivates CFS community "icons" to share what they know.   more


An Elimination Diet for CFS Patients

An elimination diet is the best method of assessing the food sensitivities that experts believe affect 20 to 50 percent of CFS patients, says Clinical Nutritionist Blake Graham. His protocol requires a few weeks' time and lots of label reading. But the insights gained may initiate a better quality of life.   more


A Short Q&A on Infection & ME/CFS

Dr. David S. Bell, MD, whose particular interest is the role of infection in ME/CFS, answers a few questions from patients. Might vaccinations set off the process?   more


Patient Perspective

Fast Forward to 2007: Update from a CFS Patient on Marshall Protocol

In July 2005, a CFS patient described her encouraging progress on the experimental - and controversial - Marshall Protocol. Here's her update.   more


Clinical Trial News

U. of Cincinnati Recruiting CFS Patients in Study of Duloxetine for Fatigue

Previous trials in Canada, Indiana, and elsewhere have studied the drug duloxetine for pain and mood in Fibromyalgia patients. The current study is focused on the drug's efficacy as a treatment for fatigue in CFS patients - with a secondary focus on pain and depression.   more


Trial of SAM-e to Enhance Antidepressant Drug Benefit Recruiting

The Mass General Depression Clinical Research Program in Boston is recruiting patients taking antidepressant drugs yet still experiencing symptoms of depression - for a study of the food supplement SAM-e's ability to enhance benefits.*   more


St. John's Wort vs. Standard Antidepressant for Minor Depression

"Feeling down or tired all day no matter how much sleep you get? Or more irritable than your usual self?" You may be suited for a new NIH-funded study of the natural herb St. John's Wort vs. Celexa®.*   more


CFS Research Abstracts

Non-Drug Studies

CFS-Related Studies

Letters From Our Readers

     CFS Q&A Session      Patient Thinking & Rethinking
Please share your thoughts with us! Send Us a Leter

Weekly Inspiration

It ain't supposed to make sense; it's faith. Faith is something that you believe that nobody in his right mind would believe. - Archie Bunker

Pacing Our Program

We can't help but be excited about our new way of life. We have made plans and we're giving it our all. Suddenly we discover our energy has run out. We wonder what has gone wrong. We realize that we have forgotten to pace ourselves. Our once vigorous energy level has not had time to rebuild itself, yet our minds thought otherwise.

Most likely we can't fix our past or determine our future in one day. We must relax and enjoy our newfound way of life and set a pace that is comfortable for us. Everything will get done and unfold in its time.

From Living With Chronic Pain One Day At A Time, by Mark Allan Zabawa


About ImmuneSupport.com

Published by ProHealth, Inc., ImmuneSupport.com is the Web's largest resource for Fibromyalgia and Chronic Fatigue Syndrome. Since 1988, ProHealth has raised and donated over 2.5 million dollars to CFS and FM research and advocacy groups seeking a cure. We believe in "commerce with compassion."

Every purchase made at ImmuneSupport.com funds research - as does every purchase made from ProHealth's Health Resource catalog.

Visit ImmuneSupport.com

If you have any comments, suggestions or ideas, please let us know. Include your full name if you agree that we might share your letter with other readers.

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* Note: This article first appeared in last week's FM Edition of CFS & FM Treatment & Research News (Jan 24, 2006)

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