Vikki Slade

I am so pleased that my hon. Friend has made that intervention, because I am just coming on to tell people about my constituent in Wimborne. He said that he, his brother and his nephew have all been diagnosed with Parkinson’s. When he was first diagnosed, he saw a Parkinson’s nurse every six months and then saw one annually. However, because there is now just one specialist Parkinson’s nurse covering my constituency, he has seen nobody for two years. Karen, who is also from Wimborne, emailed me and said that she had an appointment with a neurologist and then one with a nurse, but now faces a 14-month wait for her next appointment. Across England, as we have heard, only half of patients meet the 18-week target, even though we know that early support—physiotherapy, speech therapy and clear information—keeps people healthy for longer. If the Government are serious about transforming the NHS, they cannot allow people with progressive conditions who need a multidisciplinary approach to be forgotten. The NHS workforce plan is due in the spring. What assurance can the Minister give that neurology and Parkinson’s care in particular will feature strongly? It is great that the Government have expanded medical places, but what assessment has been made of how that will translate to neurology services? Given the training time required to generate such expertise, what is being done to bring consultants here from abroad to tackle the crisis now? In my constituency, 333 people are living with Parkinson’s. On average, each one will be admitted to hospital at least once a year, two-thirds of them in an emergency, which will mean spending a week, unplanned, in an acute bed. That is simply not acceptable and we need to do better now.