Health Funding & Support for Chronic Fatigue Syndrome (CFS) / Myalgic Encephalomyelitis (ME) & Fibromyalgia (FM)
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PLEASE NOTE IF YOU HAVE ALREADY SIGNED THE HARD COPY VERSION PLEASE DO NOT SIGN THIS ONE. THE CLOSING DATE IS 17 NOVEMBER 2011.
To the House of Representatives
“We the undersigned respectfully request that the House of Representatives consider the needs of those with Chronic Fatigue Syndrome (CFS) / Myalgic Encephalomyelitis (ME), and Fibromyalgia (FM) and support the following outcomes:
1. To establish dedicated research, assessment, treatment and respite care facilities.
2. To provide support and funding for patients and carers.
3. To promote education for both health professionals and the public, thereby rectifying the misunderstanding that many with these illnesses are experiencing, due to the lack of appropriate information regarding the cause and treatment of these illnesses.
4. To rectify the misconception that these are psychological illnesses and to acknowledge and validate, the enormous physical and emotional suffering of those afflicted with them.
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Goal
261 signatures
Goal: 5,000
Latest Signatures
15 April 2013
261.
Nick Henwood
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26 April 2012
8 January 2012
259.
Pete F
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5 January 2012
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30 December 2011
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249.
Mahn Reynolds
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7 December 2011
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243.
Lisa Fry
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21 November 2011
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