by ccisupport | May 12, 2022 | Research
Article Written By: Stuff science columnist Dr Siouxsie Wiles. Diagnosis of ME/CFS is challenging and generally requires people to have experienced symptoms for six months. With the pandemic in its third year, many people with long-Covid are now meeting the diagnostic...
by ccisupport | May 12, 2022 | Research
Otago research has established that Long Covid patients have an almost identical chemical composition to people with myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS). Those conditions had been dismissed and labelled a psychological ailment for many years...
by ccisupport | May 12, 2022 | Research
Full Article written By Patrick Hadfield – ME Auckland Post-infectious illnesses are not new. In fact, I’m writing this because 12 May is ME/CFS Awareness Day – a day chosen as it marks Florence Nightingale’s birthday. The famous nurse was...
by ccisupport | May 11, 2022 | Blog, ME Awareness Day
Two personal accounts for Mel of what it is like living with ME (Myalgic Encephalomyelitis), also known as Chronic Fatigue...
by ccisupport | May 11, 2022 | Blog, ME Awareness Day
A personal account of what it is like living with ME (Myalgic Encephalomyelitis), also known as Chronic Fatigue...
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