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?

'I Felt Like A Prisoner In My Own Home'

Thursday 18 June 2020

 

From the BBC:

 

Rebecca Browne
Rebecca Browne
 

‘I felt like a prisoner in my own home’

16 Jun 2020
Copyright © 2020 BBC.

A long-term back injury and fibromyalgia left 26-year-old Rebecca Browne unable to leave her house.

“I was like a prisoner in my own home, so I eventually had to look into getting a wheelchair,” she said.

Rebecca received a wheelchair loan through the British Red Cross Mobility Aid Service. It’s available to people when hospitals don’t have wheelchairs available for short-term use.

"There's a perception that wheelchairs are only for people that can't walk and they're for so much more than that," she said.

"When I got the wheelchair I was able to go out to the shop or go to the park."

Red Cross manager Fionnuala Molloy says there has been an increase in wheelchair loans across Northern Ireland since lockdown began.

“A lot of hospitals needed to get folk out fairly quickly so there’s been quite a quick turnaround for discharge.

“A lot of our requests are about making sure people aren’t bed-bound in their own homes or that they can at least get out to the garden, because that makes a real difference.”

Video journalist: Niall McCracken

 

 

Full article…

 


Arrow right

More Fibromyalgia News

 


Arrow right

More Multimedia

 


 

blog comments powered by Disqus
Previous Previous Page