Fleur Anderson

It is a pleasure to serve under your chairship, Ms Lewell, in this very important debate. I thank Parkinson’s UK, Parkinson’s Care and especially the “Movers and Shakers” podcast, whose dedication and campaigning led to the huge number of people signing the petition. I am sure the Minister has seen how many MPs are in the Chamber and how many people are in the Public Gallery today. Lots of people will be watching at home as well. In Putney, 163 people have Parkinson’s disease. Across the South West London ICB, 2,540 people were admitted with the disease in 2024-25. Overall, the NHS spends £325 million a year on unplanned admissions of people with Parkinson’s. This is a very big issue, which rightly deserves the attention it is getting today. I hope for some great answers from the Minister about what the NHS will be doing. First, we need more specialists for faster diagnosis. Many Members have mentioned the delays in diagnosis today, which is true in my constituency, but also in Northern Ireland, where one in 20 people wait more than five years for a diagnosis. Has the Minister spoken to the Northern Ireland Health Minister, Mike Nesbitt, about this issue? What steps are the Government taking to solve the Parkinson’s diagnosis crisis? Secondly, we need instant information. St George’s University has the vital Parkinson’s Connect resource, and it is using it, but can that be rolled out throughout the country? Thirdly, we need the Parkinson’s passport on social security. As many Members have mentioned, it is a fluctuating condition. The PIP system is failing people with Parkinson’s and their families and carers. Has that been raised with the Minister for Social Security and Disability, my right hon. Friend the Member for East Ham (Sir Stephen Timms)? Comprehensive care and more funding will allow us to deliver care, dignity and hope to everyone living with Parkinson’s and their families.