Dementia Care

Richard Baker Excerpts

Tuesday 3rd June 2025 Commons Chamber

[Mr Jonathan Brash (Hartlepool) (Lab)]

My dad was a GP in Hartlepool for 33 years. When I was young, I was never more impressed than when he would talk to me about his medical knowledge. The depth of his knowledge was extraordinary, and one of the tricks he used to be able to do at any given moment was take any two numbers I gave him and divide them or multiply them and get the answer right when I checked on the calculator. It was a rare skill, and his impact over those 33 years meant that when I went into politics the most common thing I heard on the doorstep was, “Are you the doctor’s son?” He did tell me recently that someone had asked him whether he was the MP’s dad, and I take that as a small victory.

In Hartlepool, there are 1,299 people living with dementia, and my dad is one of them. He was diagnosed with Alzheimer’s five years after he retired. Speaking to my mum, who obviously is his carer, too, we both agree that it feels like we have already gone through a form of bereavement, because the person who brought me up is not quite there any more. He is happy, and he enjoys his grandchildren, but it is different. I want to see that changed for other people, because early diagnosis is critical. My dad did not get the early diagnosis that he should have received, and we have paid the consequences as we have gone forward.

In Hartlepool, we are pioneering a new dementia strategy. I am so proud of Hartlepool borough council, because as part of that strategy, the council has committed to ensuring that 100% of its social care staff have dementia training, so that this evil disease—I do mean evil—can be caught and better treated at an earlier stage. As we have already heard from the hon. Member for South Devon (Caroline Voaden), only 29% of social care staff in this country have any form of dementia training. I impress on the Minister that that must change.

Dementia is the defining health and social care challenge of our time. It impacts one in two of us—50% of the population—either through being diagnosed ourselves, or having someone in our life diagnosed with it. Despite this reality, too many people living with dementia and their families struggle to access necessary support. The lack of an integrated care pathway often leads to families being led into fragmented and complex systems, where they can easily fall through the cracks and reach crisis point. Shockingly, one in four hospital beds is occupied by a person living with dementia, and those people face hospital readmissions at rates 50% higher than the general population. We must improve specialist dementia support, both in hospitals and in our communities. That is not just a moral imperative; it is vital for building the health service that we want, one that is fit for the future. The forthcoming 10-year health plan presents a crucial opportunity to rectify those shortcomings.

[Richard Baker (Glenrothes and Mid Fife) (Lab)]

My hon. Friend is making a powerful speech. I have worked in this area of policy and services, and I am aware that some of the most powerful advocates for change in dementia care are people with dementia themselves and their families. Does he agree that, when formulating new strategies for dementia care, people with dementia must be fully included in making those plans, based on their own experience?