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ME/CFS SOUTH AUSTRALIA INC

Registered Charity 3104

Email:
sacfs@sacfs.asn.au

Mailing address:

PO Box 322,
Modbury North,
South Australia 5092

Phone:
1300 128 339

Office Hours:
Monday - Friday,
10am - 4pm
(phone)

ME/CFS South Australia Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.

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ME/CFS South Australia Inc aims to keep members informed of various research projects, diets, medications, therapies, news items, etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives.

Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services.

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CFIDS Association of America webinar

Saturday 13 February 2010

The CFIDS Association of America is hosting a 'webinar' on Thursday 18 February in the US:

WEBINAR: CFIDS Association Research Program Update

research networkIn 2008, the Association greatly expanded its research program and launched several new initiatives. Suzanne D. Vernon, PhD, scientific director of the CFIDS Association of America, will describe the Association's approach to expanding research and the six projects it funds directly. We hope you'll join us to learn more about exciting research projects and the network that links these projects and ideas together.

Speaker: Suzanne D. Vernon, PhD, Scientific Director
Date: Thursday, February 18, 2010
Time: 2:00-3:30 (Eastern Standard Time)
Registration: https://www1.gotomeeting.com/register/668153665

Dr. Vernon will share the Association's approach to funding research and why linking independent investigators through a network will accelerate progress. She'll describe how the six projects being supported address different aspects of CFS and hold promise for improved diagnostics and treatment. Here are a few previews of her slides:

gut3Dr. Sanjay Shukla at the Marshfield Research Foundation is studying the human microbiome, testing samples taken from CFS patients before and after an exercise challenge to see if post-exertional symptoms might be due to agents crossing from the gut into the bloodstream.

light figureThis figure from research being led by Kathy Light, PhD at University of Utah shows blood markers after modest exercise in sedentary controls (top), CFS patients (middle) and MS patients (bottom).

tilt testDr. Marvin Medow and his team at New York Medical College use a tilt test and other tests of autonomic function to evaluate blood flow problems that have been reported in CFS patients. His team collaborates with Dr. Dikoma Shungu, who uses a brain imaging technique to look for abnormal levels of certain brain chemicals.

Please take advantage of this opportunity to learn more about these and other important studies, and how the Association's network of investigators is contributing valuable information to making CFS widely understood, diagnosable, curable and preventable.

To learn more about webinars in general, please visit http://www.cfids.org/webinar/what-is-a-webinar.asp. Reading this information will orient you to the technical requirements and what you can expect during the webinar. You can also keep up with new topics/dates as programs are added to the schedule at http://www.cfids.org/webinar/series2010.asp. To register for the Feb.18 webinar, go to https://www1.gotomeeting.com/register/668153665.af web

 

 

 

 

 

 

Our Mission:
For CFS to be widely understood, diagnosable, curable and preventable.
 
Our Strategy:
To stimulate research aimed at the early detection, objective diagnosis and effective treatment of CFS through expanded public, private and commercial investment.
 
Our Core Values:
To lead with integrity, innovation and purpose

Information about the Association's 2010 Webinars Series is available here.

 


 

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