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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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'Invisible Disease' Of Fibromyalgia – Campaigner Fighting For A Change In The Law
Thursday 21 December 2017
From UK newspaper The Northern Echo:
 CAMPAIGN: Alison Morton, pictured with her boyfriend James Campbell, will be taking her campaign to Parliament in the new year |
'Invisible disease' of Fibromyalgia – campaigner fighting for a change in the law
A DARLINGTON woman is taking her fight to get an ‘invisible disease’ recognised as a disability in UK law to Parliament.
Twenty-nine-year-old Alison Morton, who is chairman of the Longbenton-based Newcastle Fibromyalgia Support Group, will join a team of people next month to speak to MPs about the need for funding and research into the condition.
“We are going to speak to MPs about the desperate need for more funding, research, recognition, support and education with regards to Fibromyalgia,” she said.
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Registered Charity 3104
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