Jim Shannon

It is a real pleasure to serve under your chairship, Ms Lewell. I will show people how to do a 30-minute speech in two minutes. I congratulate the hon. Member for Colne Valley (Paul Davies) on setting the scene, and thank him for that. I am the DUP’s health spokesman, so I know many people in my constituency suffer from Parkinson’s and I know about the devastating effects it can have on aspects of their lives. I give a big thanks to Parkinson’s UK. Many of them are in the Gallery today, and I thank them for all the help that they have sent to us. I want to present some stats on three questions in the short time I have. In my constituency of Strangford there are 272 people living with Parkinson’s and a further 694 people in the South Eastern trust area. We expect that this year 98 more people will have Parkinson’s. Shockingly, around one in five people do not have proper access to a Parkinson’s specialist nurse—1,328 people in Northern Ireland. It is lovely to see the Minister in her place; I thank her for being here. My first request to her is to ensure that, as the hon. Member for North Down (Alex Easton) said, the four regions—England, Scotland, Wales and Northern Ireland—work together. We can do it better together and we should always try to do so. They say that, with adaptations, travel costs and additional energy payments, it costs almost £22,000 a year to have Parkinson’s. That is a salary. I want to highlight the issue of Parkinson’s and personal independence payments, which I deal with all the time in my office. I say this with respect: I am not quite sure whether the person who does the PIP checks has the knowledge to understand what Parkinson’s is and how PIP should be involved. That is my second ask to the Minister. There is no doubt that change is needed. My third ask is research. We are aware of the motor and non-motor symptoms that come with Parkinson’s. We must have more research. Let us find a cure in our lifetime. They say that in 10 years’ time, they will find the cure for cancer—well, let us find a cure for Parkinson’s as well. That is my hope. Timely diagnosis, specialist care and community support remain inconsistent across the region, leaving many individuals and families navigating the condition without the full resources they need.