At screening of hard-hitting film UNREST which describes the daily struggle of people living with ME. Check out #timeforunrest
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Thank you, we are in desperate need of biomedical research into this disease. Also recognition from DWP and others and training for doctors.
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And then being penalised by DWP for not seeing a specialist. How can we see a specialist when there aren't any?
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Thank you so much for your support. UK gov ME biomedical research funding staggeringly low compared to other similarly disabling diseases.
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So glad to see a Scottish MP was there. Many Scots suffering with ME and no answers.
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