Society Logo
ME/CFS Australia Ltd
Please click here to donate ME/CFS Australia (SA) Inc
 
 
Facebook
 
ME/CFS AUSTRALIA (SA) INC

Registered Charity 3104

Email:
sacfs@sacfs.asn.au

Mailing address:

PO Box 322,
Modbury,
South Australia 5092

Phone:
1300 128 339

Office Hours:
Monday - Friday,
10am - 4pm
(phone)

ME/CFS Australia (SA) 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 Australia (SA) 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 (PDF, 156KB)
Why become a member?

'Invisible Disease' Of Fibromyalgia – Campaigner Fighting For A Change In The Law

Thursday 21 December 2017

 

From UK newspaper The Northern Echo:

 

Alison Morton and James Campbell
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

By Graeme Hetherington
Chief Reporter (Tees Valley)
19th December 2017
© Copyright 2001-2017.

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.

 

Full article…

 


Arrow right

More Fibromyalgia News

 


 

blog comments powered by Disqus

Previous Previous Page