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Chronic Fatigue Syndrome/ME resource providing news, me-cfs treatment information, medical abstracts and a support community for those coping with Chronic Fatigue Syndrome/ME.
 
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Chronic Fatigue Syndrome & Myalgic Encephalomyelitis Advocacy


Chronic Fatigue Syndrome and Myalgic Encephalomyelitis Advocacy Advocacy plays an important role in any illness, but for illnesses that are not well accepted in the medical community, advocates are crucial.

Advocates are responsible for lobbying representatives to help increase research funding. They sponsor conferences, which allow researchers to share their findings and provide an avenue for physicians to stay up to date on the latest developments.

Advocates organize fund-raising campaigns for research, and increase public awareness of the illness and how it affects patients. They initiate petition drives, start support groups, and post commentary on their blogs about events that directly affect the welfare of patients.

On a personal level, advocates are responsible for making sure ill children and their families are protected, and their civil rights upheld.

Many people are too ill to do advocacy work, but anyone can participate by signing a petition, or sending an email, or by a posting a tweet when events that affect our community arise.

The cumulative effect of advocacy efforts, from organizing major fund-raising drives to simply signing a petition, is that all of our lives are made easier.

Advocacy Sites for Chronic Fatigue Syndrome & Myalgic Encephalomyelitis:


ME Advocacy
http://www.meadvocacy.org

Occupy CFS
http://www.occupycfs.com
Thoughts About ME
http://thoughtsaboutme.com

Onward Through the Fog
http://cfstreatment.blogspot.com


Chronic Fatigue Syndrome & Myalgic Encephalomyelitis Advocacy News:


Hope for Karina Hansen With Help From Save4Children
A charity is created by the editors of the ME Global Chronicle to help the parents of children who have been forced into psychiatric wards by authorities.
NIH Awards $1.3 Million to Lipkin, Klimas And Hanson for ME/CFS Research
In an unexpected move, the NIH gives $766,000 to Drs. Ian Lipkin and Mady Hornig and their team at Columbia University on August 14.
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