Doctors are to be given training in better ways to diagnose and treat people with ME, as part of a long delayed action plan that’s finally been published for people in England.
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The debilitating condition with a range of symptoms from severe exhaustion to constant pain, affects around 400,000 people in England and Wales.
Many feel they’ve been ignored and stigmatised for too long.
But with little funding allocated, is the plan enough to deliver the progress and recognition they need?
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