![]() 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. |
|
|||||||||||
'It Massively Affects Day-To-Day Life' - Living With Chronic Fatigue SyndromeTuesday 3 November 2020
From Irish radio program NewsTalk:
'It massively affects day-to-day life' - Living with chronic fatigue syndrome Chronic fatigue syndrome is something that 'massively affects' day-to-day life, according to one Irish woman living with the condition. Sarah O’Connell has been living with chronic fatigue syndrome – also known as ME (myalgic encephalomyelitis) – for the past seven years. Her nine-year-old daughter Hayley has recently been diagnosed with the same illness. Speaking to Lunchtime Live, Sarah said her own symptoms began after catching the winter vomiting bug in late 2012 – a virus from which she never seemed to fully recover. She said: "In February I got a really nasty throat infection. I just found myself going back to forth to the GP. "I just wasn't feeling myself... then they told me I had something called post-viral fatigue syndrome. Then once it progressed a little bit longer, at the year mark, they diagnosed me with ME."
blog comments powered by Disqus |
||||||||||||
|
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)