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Campaign for a Fair Name Most Find "Chronic Fatigue Syndrome" Inaccurate and Trivializing - Name Must be Changed to Gain Credibility
Nothing is more powerful than an idea whose time has come. - Victor Hugo
Dear Kerrie, Our last newsletter calling for changing the name "Chronic Fatigue Syndrome" (read FATIGUE) met with extraordinary support from the patient and medical communities. Patients and doctors alike rallied to the cause, and wrote to us to express their discontent with the present name. Most indicated they have long felt that the name "Chronic Fatigue Syndrome" trivializes the seriousness of the disease by calling it by the name of a symptom that is shared by almost everyone at some point in their life, and that a more appropriate name must be adopted in the United States.
Every single letter we received at ProHealth was critical of the name as being inaccurate and demeaning. Our busy message board resounded with a clear and unified voice: The time to change "Chronic Fatigue Syndrome" has come.
Changing the name is an idea that has waxed and waned over the past decade. Patients have complained bitterly about it for years. Doctors and researchers have never been happy with the name, and have called for a change. Even the largest CFS patient organizations have formed committees to discuss the topic. But nothing has changed.
We feel it is imperative to take it upon ourselves to make this happen - for each other, for the countless patients who suffer in agony from the debilitating disease that bears such a trivializing name, and for our friends, doctors, and loved ones who sometimes bear the humility and embarrassment right along with us.
The reservoir of knowledge and the resolve of our readers, site visitors, and bulletin board participants is formidable, and working together we are unstoppable. This is exactly what we need in order to get the job done. ProHealth is calling on you - on all of us - to do our part to change "Chronic Fatigue Syndrome" to something we can all agree on, and is today launching "Campaign for a Fair Name." That campaign begins here, today, and it will end - successfully - when the name is changed, once and for all.
You and other volunteers are needed. ProHealth will commit to providing much of the funding to get the job done. And if you want to help, e-mail us at CFSnamechange@.... Please include your name and contact information. We'll get back to you with more information on next steps as the project gets underway.
Our cause is lost without your support. Without volunteers we will not succeed.
Rich Carson CFS patient; ProHealth Founder
Meet the Patient
Meet CFS & FM Patient Sheila Cruthirds, a ProHealth Team Member
Sheila struggled more than a decade to resolve the mystery of her symptoms. Then, by accident, she found a physician whose review of clinical research led to a diagnosis.*
40 Percent Improvement in Energy Follows Dietary Supplementation to Support Cellular Function
Individuals with CFS and/or FM receiving the dietary supplement NT Factor® in a two-month clinical trial achieved improvements in energy averaging more than 40 percent, as measured by the Piper Fatigue Scale.*
Author and wellness consultant William Collinge, PhD, has observed 10 principles "that seem to lay a foundation for exceptional healing," during more than a decade working with CFS and FM patients.
Researchers at Columbia University in New York have identified a protein in nerve cells that acts as an "on/off switch for chronic pain." They've applied for patents to develop a new class of drugs that they predict will block chronic pain by turning this switch off.
Seventy percent of patients with migraine onset symptoms who received a painless one-millisecond pulse of magnetic energy reported little or no pain at two hours post-treatment.*
The Difficulty of Differentiating Lyme Disease from CFS and FM: Finding a Reason Behind the Pain
Shawn Stevenson might be close to a diagnosis of Lyme Disease vs. CFS or FM after 11 years of unexplained pain, scores of tests, and fruitless consultations with 20 doctors.*
Are Your Elected Representatives Supporting CFS in Washington?
So far 29 members of the House of Representatives and 11 Senators have communicated their support for continuation of the federal CFS Advisory Committee's work. The deadline for renewal is September 5, and it's our turn to back them.
Those of us who face our pain and our limitations each day are known as those who dare. We dare to face the known and the unknown, the believable and the unbelievable, the powerful and our powerlessness.
We who dare face decisions of altering our lives and having our lives altered for us without warning. We are those who dare to try a new beginning and dare to follow our passions and unfulfilled dreams.
From Living With Chronic Pain One Day At A Time, by Mark Allen Zabawa
Your Feedback Counts!
At ProHealth we are committed to bringing you the most up-to-date information on Chronic Fatigue Syndrome and Fibromyalgia. We are always striving to improve our services, and your opinion counts. If you have any comments or suggestions, please let us know.
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.
ProHealth, Inc. 2040 Alameda Padre Serra, Suite #101 Santa Barbara, CA 93103 USA Customer Service: 1 (800) 366-6056 International: 001.805.564.3064 Fax: 1 (805) 965-0042
~*Kerrie*~
Owner: Rhode Island Fibromyalgia-CFS Support Group on Yahoo Click the link to join or just to check out the group! New members welcome! This group is for ANYONE with Fibromyalgia/CFS, you do NOT have to be from Rhode Island to join!!! http://health.groups.yahoo.com/group/RHODE_ISLAND_FIBROMYALGIA-CFS_SUPPORT/
We are here to do good, help others, then shut up and GO HOME! --Sylvia Browne www.sylvia.org
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