Society Logo
ME/CFS Australia Ltd
Please click here to donate ME/CFS South Australia Inc
 
 
Facebook
 
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.

Disclaimer

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.

Become a Member
DOCX Application Form (Word, 198 KB)
Why become a member?

The Kaplan Center: Understanding And Treating ME/CFS

Thursday 16 July 2015

 

From The Kaplan Center for Integrative Medicine:

 

The Kaplan Center
 

Understanding & Treating Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Published on 5 Feb 2015

It is estimated that over 1 million people in the United States are living with Chronic Fatigue Syndrome (Myalgic Encephalomyelitis Chronic Fatigue Syndrome, ME/CFS). CFS is a debilitating disease characterized by extreme fatigue and a host of other symptoms such as sleep disorders, muscle pain, headaches, swollen lymph nodes and sore throat, to name a few. These symptoms can worsen after physical or mental activity and do not improve with rest. There is no known cause for CFS and despite advances in research a cure remains elusive with treatment primarily focused on providing relief.

People living with CFS, the majority of whom are women, face challenges in every aspect of life. Productivity suffers both at home and at work, relationships with family members and friends often deteriorate and the ability to actively engage in many of life’s activities is compromised. Many people with CFS are looked upon as lazy or delusional by their peers, and tragically even health care providers have doubted CFS to be a legitimate illness. This stigma along with losing one’s sense of accomplishment can cause depression and further one’s sense of despair. The effects of CFS can devastate a person’s quality of life for many, many years.

Dr. Gary Kaplan, a member of the Department of Health & Human ServicesChronic Fatigue Syndrome Advisory Committee (CFSAC), shares his view on the challenges of diagnosing CFS and what needs to be done differently to advance its treatment.

Dr. Kaplan also comments on the recent findings of the National Institutes of Health’s (NIH) Pathways to Prevention conference “Advancing the Research on ME/CFS,” which was held on Dec 10, 2014.

Part 1 of 3
Part 1: What's In A Name? ME vs CFS? Defining ME/CFS & Diagnostic Criteria

 

Part 2 of 3
Part 2: ME/CFS: Neuro Inflammatory Disease? Getting a Valid Diagnosis

 

Part 3 of 3
Part 3: Potential Causes & Comprehensive Treatment Plans

 

The above originally appeared here.

 


Arrow right

More Multimedia

 


 

blog comments powered by Disqus
Previous Previous Page