![]() 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. |
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Long Covid: 'I Don't Have A Life, I Currently Have An Existence'Sunday 18 October 2020
Long Covid: 'I don’t have a life, I currently have an existence' A woman being treated for chronic fatigue after having presumed Covid-19 has called for urgent research into the impact of the virus. Annette Shelford, 48, from Cambridge, had two weeks of "non-stop pain" after a fever in March and said she had suffered severe problems ever since. "We urgently need recognition, research and rehab for people like me who are still struggling," she said. The government said it recognised the impact of Covid-19 on long-term health. Ms Shelford, a former fitness instructor, said after developing symptoms she followed government advice, self-isolated for two weeks, and did not call the doctor or NHS 111. A day later, her symptoms returned. "It was like being hit by a steam-roller. All the pain came back, with new symptoms, and it's been a journey like that for the past six months," she said. She was not able to confirm it was coronavirus as it was before mass testing was available, but said doctors who had been treating her were referring to her illness as post-Covid.
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Registered Charity 3104
Email:
sacfs@sacfs.asn.au
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