Vikki Slade

It is a pleasure to serve under your chairmanship, Ms Lewell. Imagine being told that you have a progressive, incurable condition and then waiting over a year just to see a specialist. That is the reality for so many people with Parkinson’s and the number of people with Parkinson’s is set to double by 2050. When my constituent Carol was diagnosed with Parkinson’s in 2009, she was only 46 years old. Consultants told her then that they hoped a cure might come within a decade, but 16 years later there is nothing. At this point, I must declare an interest. My daughter Molly is a PhD researcher with a brilliant team at the University of Southampton that is working to understand Parkinson’s, so that better treatments and cures can be found. As a member of the all-party parliamentary group on Parkinson’s, I know that great work is also happening elsewhere, particularly through the Brain Bank at Imperial College London. However, research alone is not enough; people living with Parkinson’s need care now. Just before the general election last year, the current Secretary of State for Health and Social Care, then in his shadow role, admitted in the “Parky Politics in the Pub” podcast that there were not enough neurologists and committed to fix it. He said: “We campaigned hard on workforce to get the last Government to commit to doubling the number of medical places so we can train up staff—especially in neurology, where we have shortages.” He said he would deliver that workforce plan, yet today waiting times are unacceptably long—not just for initial appointments, but for ongoing care.