Dementia Care

Vikki Slade Excerpts

Tuesday 3rd June 2025 Commons Chamber

[Vikki Slade (Mid Dorset and North Poole) (LD)]

Dementia is such a cruel disease. Let us be clear that it is not simply part of getting old, yet too often it is treated as though it is inevitable. In my constituency the number of people living with dementia is nearly 40% higher than the national average. One in every 45 adults of all ages has been diagnosed, and we know that the true number is even higher when we include those not diagnosed.

Family members, who provide such amazing care, are relying so heavily on community groups such as Stepping Stones—led by my predecessor and good friend, Dame Annette Brooke—with jigsaws and its tea dances providing moments of joy. The Leonardo Trust provides grants for unpaid carers, and I thank the Museum of East Dorset for its fantastic work in recruiting residents to crochet the over 8,000 forget-me-nots that decorated the town of Wimborne last month.

Neurological conditions such as dementia are the leading cause of illness globally, and as our population ages, the challenge will only grow. However, dementia is not just a disease of old age—some of the most heartbreaking cases are among younger people. A neighbour of mine in Broadstone—a proud veteran, builder and father—was diagnosed in his early 50s. I watched him go from walking past our house without recognising us, to needing a carer by his side and now living full-time in a care home. His daughters, who once played with mine, will never have their father walk them down the aisle and his wife will never share the retirement they dreamed of.

That is why I did not hesitate to become a dementia research champion. If we do not understand how the brain works and how to stop it failing, we will not get the benefits of extended life expectancy. Today, the Daily Mirror has reported that over 100 new drugs are in development to halt dementia, with scientists saying we are at the start of a journey to a cure. Of these drugs, 86% could halt or reverse the disease. However, research alone is not enough, and we must transform the care we give.

Like those of other Members, my constituents are facing a battle just to get the care they need. Andrew was told that his wife Tricia did not qualify for NHS continuing healthcare because it did not meet the NHS-funded nursing criteria of being short term or of optimum potential, despite changing on a daily basis. The council eventually stepped in, but not until Andrew himself had become ill. Why is nursing care not being picked up by the NHS? Surely that is what it is for.

Another constituent, Emma-Jane, told me about her mother, who has dementia and paranoia, and has become abusive. Her father, who had protected his family for so long, once spent the night in a park just to escape. A social worker decided that her mother could not go into a care home, because her mother had wanted to stay at home, despite acknowledging that she lacked the capacity to make such a decision. After accessing respite care when the family reached crisis, Emma-Jane is now funding care privately, while she battles the council because her father simply cannot cope. This is intolerable: families are breaking and councils are overwhelmed.

Kevin wrote to me about his Aunt Jean, now 92, who entered a care home eight years ago. The family home has gone and the money has gone, so the council must step in, but the care home fees are nearly double the local authority cap. Even with Jean’s pension and a discount from the care company, there is a £300 a week shortfall, leaving the family to choose between paying out of their own pocket or moving her from the place she has called home for nearly a decade. To put that into perspective, the cost of caring for Jean for one year, after her pension contribution, is equivalent to the total annual council tax of 24 households. If every dementia patient in my constituency needed council tax funded care, it would consume the council tax of 43,000 homes, and I have only 44,000 in the whole constituency.

We must act: we must invest in research, support carers, and reform how we fund and deliver care. I call on the Minister to push for faster progress on the Casey report. There is no choice: the cost of inaction is too high for our families, our communities and our country.