Society Logo
ME/CFS Australia Ltd
Please click here to donate ME/CFS South Australia Inc
 
 
Facebook
 
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.

Become a Member
DOCX Application Form (Word, 198 KB)
Why become a member?

Desperate UK Woman In Agonising Pain Waiting Months To Know If She's 'Disabled Enough' For Benefits

Sunday 22 September 2019

 

From UK news outlet Hull Live:

 

Patricia Nimmo
Patricia Nimmo says she has been fighting the DWP for
PIP payments since she had to stop work in 2016.
(Image: Jerome Ellerby)
 

Desperate Hull woman in agonising pain waiting months to know if she's 'disabled enough' for benefits

Patricia Nimmo wants an answer from the DWP

By Anna Riley
21 September 2019
© 2019 Local World.

A Hull woman in so much pain she struggles to walk, talk and move her hands, says she feels suicidal after waiting to find out if she is "disabled enough" for benefits.

Patricia Nimmo, 62, who served in the Armed Forces and the police, suffers with severe arthritis in her hands, which makes it very difficult and painful for her to move her fingers and thumbs.

She has also been diagnosed with fibromyalgia, which causes widespread pain around her body, and makes it a struggle for her to talk, walk and think at times.

She says her condition is so bad she can barely leave the house.

But despite doctors' evidence suggesting she is too disabled to work, Mrs Nimmo says she has been waiting for more than seven months for the Department for Work and Pensions (DWP) to determine whether she will lose her Universal Credit payments if she is deemed eligible for work.

 

Full article…

 


Arrow right

More Fibromyalgia News

 


 

blog comments powered by Disqus
Previous Previous Page