Society Logo
ME/CFS Australia Ltd
Please Click Here To Donate ME/CFS Australia (SA) Inc
 
Facebook
 
ME/CFS AUSTRALIA (SA) INC

Registered Charity 698

Email:
sacfs@sacfs.asn.au

Mailing address:
PO Box 28,
Hindmarsh,
South Australia 5007

Office:
Suite 506,
North Terrace House,
19 North Terrace,
Hackney, SA, 5069


Phone:
1300 128 339

Office Hours:
Wednesdays, 11am-3pm

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
PDF Application Form (PDF, 277KB)
Why become a member?

Gabriella nominated

Monday 13 August 2012

 

From UK newspaper Fenland Citizen:

 

Gabriella Wheeler
Gabriella Wheeler suffers from fibromyalgia and
has made a documentary about her condition.
(www.fenlandcitizen.co.uk/buyaphoto)

Gabriella nominated

Published on Wednesday 1 August 2012 06:01

A YOUNG March woman living with a painful medical condition has been nominated for an award after returning to education and making a documentary to raise awareness of her illness.

Gabriella Wheeler (20), of Cavalry Drive, dropped out of school at the age of 14 after struggling to cope with the pain of her condition – recently diagnosed as Fibromyalgia – and low self esteem from dyslexia.

She was put forward for the Cambridgeshire Constabulary Young People of the Year awards (YOPEY) by her tutor at Peterborough Regional College, where Gabriella is studying media.

Steph Ward, a personal learning coach at the college, said: “She has worked so hard to achieve her goals overcoming all the obstacles in her way. She is an inspirational young lady.”

Gabriella has nearly finished a documentary on Fibromyalgia, an incurable condition that results in pain all over the body and extreme tiredness.

She said: “Although you can’t see it, I have a lot of fatigue and pain and it’s hard to get medical support as many doctors don’t recognise it.

“I suffer from headaches, sickness, pain and dizziness on a daily basis and take high doses of painkillers and sleeping tablets to manage it.”

In addition to her documentary, Gabriella is involved with organising an awareness day with the March Fibromyalgia support group, which will be held in West End Park in September.

Pam Stewart, chair of the Fibromyalgia Association, said the work being done by Gabriella was very impressive and could potentially help thousands of people, as they would no longer have to suffer alone.

All YOPEY prizes are shared with the community. So the Cambs Young Person of the Year will win £800 ­– £400 for themselves and £400 for their good cause. The total prize pot is over £2,000.

To nominate someone aged between 10 and 25 for a YOPEY award, visit www.yopey.org or write to YOPEY, PO Box 236, Newmarket, CB8 1DP for paper entry form. Entries close on August 31.

The March support group usually meets at the library.

For more information, contact the library in the first instance.

 

The above, with comments, originally appeared here.

 


Arrow right

More Fibromyalgia News

 


 

blog comments powered by Disqus
Previous Previous Page