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?

UK Teen Tells How Life Changing Illness Kept Her Bed-Bound For Nine Months

Wednesday 15 May 2019

 

From UK news outlet Staffordshire Live:

 

Maddie Sharpe
Maddie Sharpe has spoken to Staffordshire Live
about her daily struggles.
(Image: Maddie Sharp)
 

Stafford teen tells how life changing illness kept her bed bound for NINE months

The brave 18-year-old is raising awareness about the condition

By Nigel Slater
14 May 2019
© 2019 Local World.

A Stafford teenager who was home-bound for two years and had to miss school due to suffering from a life changing illness is now running her own business after showing remarkable bravery.

Maddie Sharpe, now 18, was unable to get out of bed for nine months when she was diagnosed with an illness called M.E at the age of 13.

Her symptoms were so severe that at the age of 13, she had to rely on her mum to shower her everyday and change her clothes.

The illness, which affects around 250,000 people across the UK, stands for Myalgic Encephalomyelitis and is described as “a devastating multi-illness which causes energy depletion and severe physical and cognitive limitations”.

Fighting the illness was hard as it made Maddie very tired everyday – sometimes when she had done little activity - but she managed to start college in 2016 and did two years part time. Though a struggle this got Maddie back on track.

And now Maddie, with the help of her family, is using her skills and courage to run her own business which involves designing metal artwork.

 

Full article…

 


 

blog comments powered by Disqus
Previous Previous Page