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ME/CFS Australia Ltd
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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.

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.

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May 12 Is International Awareness Day

Tuesday 12 May 2020

 

From May12.org:

 

May 12: International Awareness Day
 

May 12: International Awareness Day

12 May 2020

MISSION

Our mission is to raise Global Awareness and Education for Complex Immunological and Neurological Diseases (CIND) including the following:

  • Lyme Disease - LD/Chronic (or late stage) Lyme Disease - CLD
  • Myalgic Encephalomyelitis – ME
  • Fibromyalgia - FM
  • Gulf War Illness- GWI
  • Mold/Biotoxin illness
  • Multiple Chemical Sensitivity - MCS
  • Chronic Fatigue Syndrome - CFS
  • Post-Sepsis Syndrome
  • Vaccine Injuries

We believe that raising awareness of neuroimmune diseases will increase funding for research, provide for better treatment, and eventually lead to a CURE for these debilitating, disabling and often “invisible” diseases.

GOALS

Our goals to raise AWARENESS and Education include:

EDUCATION, IDENTIFICATION, & PREVENTION

  • Educating medical personnel, pharmacists, hospitals (for better treatment) and the public on the facts of these diseases (many symptoms, seriousness & debilitation) and research being performed.

  • Raising awareness of the need for funding research to identify proper biomarkers for valid diagnosis and clinical trials.

  • Advocating for more thorough testing of blood and neurological biomarkers that specialists perform to help monitor and treat symptoms of this disease group along with ruling out other conditions with similar symptoms. The majority of doctors are not educated on which biomarkers to evaluate.

  • Prevention of medical abuse and neglect

 

Full article…

 


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