![[]](/sites/all/modules/ubercart/uc_cart/images/bullet-arrow-up.gif "Expand cart block."){kind=icon}
There are no products in your shopping cart.
CBS Evening News, 2/23/11 re: Study showing 700 unique proteins in CSFluid of people with CFS
Thu, 02/24/2011 - 11:38am
February 23, 2011
Research breaks Chronic Fatigue stereotypes
New study found indicators of disease unique to Chronic Fatigue Syndrome patients
Like this Story? Share it:
Play CBS Video Video New study on Chronic Fatigue Syndrome
Researchers have found protein indicators that could be a result of Chronic Fatigue Syndrome, a disease often dismissed by some medical professionals. Michelle Miller reports on the promising study.
(CBSNews)
NEW YORK - Four times a day, for the last 16 years, Maria Brant takes an assortment of supplements and medications to combat the symptoms of exhaustion, lack of concentration and muscle aches.
She has Chronic Fatigue Syndrome, a disease often dismissed and misunderstood by some medical professionals, even one of her own doctors, reports CBS News correspondent Michelle Miller.
"He said, 'lots of women are tired,'" Brant said. "I knew that I was different."
For Brant and as many as 4 million Americans afflicted with CFS , today science offers tangible proof that they have a disease.
"This study says there is a physical root cause or effect to this disease," said Dr. Steven Schutzer, with the University of Medicine and Dentistry of New Jersey and a study author.
Researchers examined the spinal fluid of CFS patients, healthy people and patients afflicted with a similar disorder - Lyme Disease. They found over 700 proteins, or indicators of disease, unique to CFS patients alone.
Dr. Nancy Klimas runs a support group for CFS patients in Miami. She can finally tell her patients that science has validated their symptoms, and one day they could be tested for it.
"We haven't had something we could just draw blood in a tube and let us measure [and say] 'Ah-ha! You must have Chronic Fatigue Syndrome,'" Climas said.
Once researchers design that test, they can zero in on a cause and develop better treatments. And not soon enough for Maria Brant.
"Talk to me in two years about this study, then we'll see," Brant said.
© 2011 CBS Interactive Inc.. All Rights Reserved.
__________________
Live and Learn. Learn and Live Better! is my motto. I'm Mardy Ross, and I founded Lumigrate in 2008 after a career as an occupational therapist with a background in health education and environmental research program administration. Today I function as the desk clerk for short questions people have, as well as 'concierge' services offered for those who want a thorough exploration of their health history and direction to resources likely to progress their health according to their goals. Contact Us comes to me, so please do if you have questions or comments. Lumigrate is "Lighting the Path to Health and Well-Being" for increasing numbers of people. Follow us on social networking sites such as: Twitter: http://twitter.com/lumigrate and Facebook. (There is my personal page and several Lumigrate pages. For those interested in "groovy" local education and networking for those uniquely talented LumiGRATE experts located in my own back yard, "LumiGRATE Groove of the Grand Valley" is a Facebook page to join. (Many who have joined are beyond our area but like to see the Groovy information! We not only have FUN, we are learning about other providers we can be referring patients to and 'wearing a groove' to each other's doors -- or websites/home offices!) By covering some of the things we do, including case examples, it reinforces the concepts at Lumigrate.com as well as making YOU feel that you're part of a community. Which you ARE at Lumigrate!
print
e-mailThis forum is provided to allow members of Lumigrate to share information and ideas. Any recommendations made by forum members regarding medical treatments, medications, or procedures are not endorsed by Lumigrate or practitioners who serve as Lumigrate's medical experts.
