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People in Wales living with Parkinson’s disease are not getting a good enough level of care, says David Chadwick.
The Brecon, Radnor and Cwm Tawe MP paid tribute in a Westminster Hall debate yesterday to everyone in Wales and across the UK who has campaigned hard for people living with Parkinson’s.
Video from parliamentlive.tv

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00:00Thank you Madam Chair. I want to make tribute to everyone in Wales and across the United Kingdom
00:07who has campaigned so hard for people living with Parkinson's. In Wales we expect the number
00:12of people living with Parkinson's to rise to more than 9,000 by 2030 and yet too many still face a
00:19postcode lottery in accessing the most basic elements of care from diagnosis to rehabilitation.
00:25Welsh health boards do not have reliable plans to replace specialist staff when they leave
00:30which means long gaps in access to expert care. Combined with ongoing shortages in neurology
00:37people can wait far too long to see anyone with the right expertise. For a degenerative condition
00:44that demands regular and specialist review this is simply unacceptable. Wales saw some of the highest
00:52disruption to rehabilitation services during the pandemic and many of those pressures have not
00:57fully eased. People with Parkinson's still report difficulties accessing physiotherapy, speech and
01:03language therapy and occupational therapy. When rehabilitation breaks down people deteriorate
01:09physically, mentally and socially and carers are left to carry an enormous burden. Many are older
01:15spouses whose own health is already fragile and they deserve a system that recognises and supports them.
01:23We must also fix the basics. In Wales 73% of people with Parkinson's in hospital say that they do not
01:31receive their medication on time. A delay of just 30 minutes can make the difference between going home
01:37or staying another week on a ward. This should not be happening.
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