Myalgic Encephalomyelitis

Tom Morrison Excerpts
Wednesday 19th November 2025

(1 day, 9 hours ago)

Westminster Hall
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Adam Dance Portrait Adam Dance (Yeovil) (LD)
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It is a pleasure to serve under your chairmanship, Mr Mundell. I thank my hon. Friend the Member for Wells and Mendip Hills (Tessa Munt) for securing this vital debate and for her campaigning on this issue. In the brief time I have today, I will share the story of Iona, who was finally diagnosed with ME in 2019 after being unwell since 2014. Her ME comes with a range of horrible symptoms from physical and mental fatigue to muscle weakness. She was housebound for four years and cannot do anything independently. However, she told me that the biggest barrier to support is other people’s limited or incorrect knowledge of ME, which is damaging. She says:

“As a chronically ill young woman…I am constantly looked down on and dismissed, while at the same time expected to act as if I am not disabled”.

Tom Morrison Portrait Mr Tom Morrison (Cheadle) (LD)
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One of my constituents, Nick, has ME and has described feeling as though he is stuck in a well without anyone to pull him out. Does my hon. Friend agree that there needs to be more action from Government, the NHS, businesses, schools and colleges to counter the misunderstanding and neglect that ME sufferers receive?

Adam Dance Portrait Adam Dance
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I agree. It is really important that the Government provide more support for ME, because it affects the lives of a lot of people.