Join us on Friday 27 June at 1pm for this rescheduled online event. We will hear from Russell Fleming, head of project development, at The ME Association. Russell has had ME (Myalgic Encephalomyelitis/Encephalopathy)/CFS (Chronic Fatigue Syndrome) for 25 years and was able to return to work 10 years ago, first as a volunteer and now […]
Join us to hear from Dr Katrina Pears, Research Coordinator for The ME Association, about the latest research into Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Long Covid. Her overview will draw on the evidence-based NICE Guideline, expert medical opinion, and findings from research into the underlying disease mechanisms. The ME Association provides effective support and […]
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