Mohammad Yasin

I want to thank my constituent Ruth, who attended my recent drop-in surgery and asked me to speak today about an issue that is personal not only to her, but to my family and thousands of other families in my constituency and across the country. Ruth was diagnosed with Parkinson’s in March 2023 after a long, fragmented and exhausting journey. She went from GP to GP, and from test to test, waiting months and years for appointments. As her symptoms worsened, she felt that she had no choice but to seek a private neurologist, and she finally received the diagnosis that changed her life. Community, information and honesty are the things that have helped Ruth since. That is why the “Movers and Shakers” podcast and organisations such as Parkinson’s UK are so important. Public figures speaking openly about related issues such as depression, the fear of falling and navigating care have cut through the stigma and reached thousands who felt unseen. The Parky charter sets out clear, reasonable asks: faster access to consultants and follow-up care; clear guidance on diagnosis; a Parkinson’s passport to ease access to support; and timely access to physiotherapies, speech therapies and wider services. Parkinson’s is the fastest growing neurological condition in the world. We need Parliament to act now. Families are asking for a system that does not leave them waiting, fighting or falling through the cracks.