ME/CFS AUSTRALIA (SA) INC
Registered Charity 698
PO Box 28,
South Australia 5007
North Terrace House,
19 North Terrace,
Hackney, SA, 5069
1300 128 339
Closed over Christmas
(reopened 1 February 2017)
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.
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.
'I Went From Being A Salsa Dancer To Someone Who Couldn't Put On My Own Socks'
Friday 13 January 2017
'I went from being a salsa dancer to someone who couldn't put on my own socks'
With 13pc of the Irish population affected by chronic pain, Deirdre Ryan sheds a light on what it's like living with fibromyalgia and rheumatoid arthritis
This is not a sob story, I'm not trying to get your vote, or win The X-Factor. My story is one of hope and resilience. My journey started eight years ago when I was 25, with a very gradual dull pain in my lower abdomen and groin.
I was an active, typical 25-year-old. I salsa danced, worked out, travelled, and worked hard in an insurance company. I thrived on being busy and social. All my blood tests were clear, an X-ray was clear, and yet the pain, becoming sharper, didn't ease without analgesics.
Then the fatigue set in, a wash of lethargy that swept over me like a black glue where every movement was an effort and I began to ache. A bone ache deep in my joints, I was sensitive to even touch. My whole system went haywire.
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