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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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UK online petition for ME/CFS sufferers

Monday 5 July 2010

GoPetitionAn online petition has been created by Simon Benson:

Justice for CFS/ME sufferers

Published by simon benson on May 29, 2010
Category: Health
Region: United Kingdom
Target: to send to Parliament

Background (Preamble):

I have been suffering from CFS/ME for the past 8 years. I was only diagnosed as suffering from the above condition 3 years ago, mainly through lack of professional medical knowledge.

CFS/ME sufferers will experience symptoms that will effect brain and nervous system, muscle symptoms include pain, exercise intolerance and post-exertional malaise (i.e. feeling fatigued the day after undue physical activity), cardiovascular and muscular deconditioning, nausea, overwhelming daytime fatigue, increased muscle tension, headaches, sleep pattern problems, also will develop emotional lability or mood swings, anxiety, panic attacks etc. There are a vast array of symptoms too many to list here which affect people differently.

Petition:

After suffering with CFS/ME for so long and after lack of treatment, support and help for this condition I have decided to draw up a petition in order to send to the Health Minister over our concerns with lack of funding and awareness of CFS/ME.

We need to know what is the cause of this illness, how we can cure this illness and also how we can prevent this illness in the future, how to make everyone more aware of cfs/me. We need better treatment facilities, and help with finance and benefit problems.

I am in talks with our local MP Steve Rotheram who will be taking the petition to Parliament so that our concerns can be highlighted with the new coalition Tory/Lib Democrat Government.

Please could you sign and ask other family members and sufferers to sign also, because it is about time we the patients made our government aware of how debilitating and serious our illness is.

Thank you for all the support and hopefully if we keep on complaining our voices will be heard and one day we will all be cured.

You can sign the petition here.

 


 

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