Madeleine Moon
Main Page: Madeleine Moon (Labour - Bridgend)Department Debates - View all Madeleine Moon's debates with the Northern Ireland Office
(9 years, 3 months ago)
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The Prime Minister
I will look at this case. It sounds as if it is a very sad case but, I am afraid, not an isolated case. As the Welsh National Audit Office found, overall, Welsh patients face shorter waits for treatment in England than they do in Wales. That is a fact. What we need is a change of direction in Wales from the Labour Administration: instead of cutting the NHS, they should be investing in the NHS; instead of leaving the bureaucracy in place, they should be taking it out of the NHS. In short, they should be taking a different track, so that we give people a better NHS.
Mrs Madeleine Moon (Bridgend) (Lab)
Yesterday, Mr Speaker graciously allowed the all-party parliamentary group on motor neurone disease to use his state apartments for the launch of its report, which demonstrates that people with motor neurone disease are having grave problems accessing the funding available for communication support in England. Some 30% of people with motor neurone disease will die within a year, and 95% will lose their voice. Will the Prime Minister meet the Motor Neurone Disease Association to sort out why these delays are happening in NHS England? Will he agree to fund communication support so that the association can provide it quickly and effectively while the NHS gets its act in order, so that no one dies without being able to communicate their last thoughts to their loved ones?
The Prime Minister
First, let me commend the hon. Lady and others across the House for the work they do on motor neurone disease. Anyone who has known someone who has suffered from that disease—as I have—realises that it is a most appalling, debilitating condition, which is very difficult for families to cope with. I will certainly look at the report the hon. Lady has produced and make sure that the proper meetings are held with the Department of Health, so we do everything we can to support these people and allow them, as she says, to communicate with their families up until the last moment.