Dementia Care

Chris Bloore Excerpts

Tuesday 3rd June 2025 Commons Chamber

[Chris Bloore (Redditch) (Lab)]

I thank the hon. Member for South Devon (Caroline Voaden) for securing this important debate, which shines vital light on an issue that affects so many families across this country, especially in my constituency of Redditch and the villages.

Over 900,000 people in the UK are currently living with dementia, and by 2040 that number is expected to rise to 1.6 million. However, the challenge is not just the growing number of people affected, but the poor support that many receive and the inequalities that persist in diagnosis and care. It is estimated that only about 65% of people aged 65 or over who are thought to have dementia actually have a recorded diagnosis, which means that far too many people are missing out on vital help early on. That is especially true in communities including ethnic minorities and in deprived areas.

I have been contacted by many families in Redditch who describe the distress of waiting months—sometimes years—for a diagnosis or clear guidance on what to do next. One particularly heartbreaking aspect is the many families who are forced to sell the home of a parent who no longer knows that they cannot return home. These homes often represent a lifetime of memories, yet families face that heartbreaking decision simply because the system does not provide adequate care options.

A particularly worrying fact cited by Age UK is that 19% of people it spoke to were concerned about accessing dementia services—they did not know where to turn or felt unable to get the support they needed. We also have to confront the huge variation in care home capacity across England’s integrated care board areas. In some parts of the country, care home availability simply cannot meet demand, limiting options for people with dementia and their families. This postcode lottery means that some people wait longer or must travel far from home for care, which is unacceptable.

The challenges faced by our NHS are also starkly evident in dementia care. Too many patients with dementia are caught up in the crisis of corridor care, where beds are not available and patients wait in hospital corridors for hours or even days. It is deeply distressing for patients and their families, and exacerbates the risk of deterioration. Such failures are a direct consequence of years of under-investment in our NHS, which has stretched resources to breaking point.

My own mother served in the NHS for 40 years. She witnessed at first hand both its strengths and its struggles. I know how deeply committed this Government are, just as the then Government were in the late 1990s, to rebuilding and reinvesting in our NHS. The recent commitments to increase funding and recruit more staff are steps in the right direction, but we must ensure that translates into real improvements in dementia care on the ground.

[Mark Sewards (Leeds South West and Morley) (Lab)]

My hon. Friend is making a powerful speech. One of my constituents has a grandma who waited a staggering 18 months for a dementia diagnosis. The family did not have the £3,000 required to get a private diagnosis. My hon. Friend mentioned the need to increase the resources available to the NHS and how committed this Government are, so will he join me in encouraging the Minister to direct resources not just to dementia care, but to dementia diagnosis, so people can get the diagnosis they need faster?

[Chris Bloore]

My hon. Friend’s intervention highlights inequalities throughout the country and reaffirms why the hon. Member for South Devon sought this debate. People who cannot access private care are put at a huge disadvantage, which is simply not acceptable, so I agree with my hon. Friend’s call to the Government.

We know that people with dementia are far more likely to have unplanned hospital admissions, which can cause distress and often worsen their condition. That shows why we urgently need better community care, and why hospital staff must have improved dementia training to provide the care that these patients deserve.

The economic cost of dementia to the UK is enormous; including healthcare, social care and the wider costs to society, it is estimated to be over £42 billion a year. The huge financial burden highlights the importance not only of investing in medical research but of improving support and care infrastructure.

Unpaid carers play a massive and often overlooked role. In fact, family members and friends provide the majority of care for people living with dementia. Women make up a disproportionate share of unpaid carers, balancing that demanding role alongside work and other responsibilities. Their contribution is invaluable but can come at a significant personal cost, including financial strain, mental and physical exhaustion, and social isolation.

Age UK has made it clear that the system is overstretched and underfunded. People in Redditch, and everywhere else, deserve consistent, high-quality care that respects their dignity no matter where they live.

[Matt Rodda (Reading Central) (Lab)]

My hon. Friend is making an excellent speech. In particular, I commend him for the way in which he has talked about the support that relatives often give as caregivers. Will he elaborate a little further on the points he made about the need for more resources to be focused on less advantaged communities? My own experience in representing a community that has some disadvantages is that people in those communities, particularly families from ethnic minority backgrounds, need far more support.

[Chris Bloore]

I completely agree. It is clear from the data that disadvantaged communities and those from ethnic minorities are not getting the targeted support that they need; I see that in my constituency, particularly in the Winyates district of Redditch. The data shows a very clear reason for further intervention.

Diagnosis is only the start. The Alzheimer’s Society calls for a minimum standard of good quality post-diagnosis support, but real faults remain. Too many people receive little or no clear information after diagnosis. They are left to navigate a confusing maze of services alone, with inconsistent follow-up and limited access to support groups or counselling. That gap leaves families isolated and unsure about managing symptoms or planning for the future, increasing stress and uncertainty during a profoundly difficult time.

Carers also bear an incredible burden. Families in Redditch tell me about exhaustion and isolation. We need better respite care, as the hon. Member for South Devon said, and better financial support and mental health services for carers. Too many of my residents rely on the voluntary sector for support in their communities; I particularly commend the Astwood Bank memory café for the work that it does.

We must improve the skills of those caring for people with dementia. The Alzheimer’s Society calls for mandatory, high-quality dementia training for all adult social care workers. Hospital staff need better access to dementia training too, because too many patients experience distress and delays because staff do not have the skills that they need.

Importantly, dementia must have parity of esteem with cancers in funding and Government prioritisation. Dementia affects millions and carries a massive societal and economic cost. It deserves the same urgent intention, investment and commitment that cancers receive so that research, care and support can improve in step.

While investing in research is important, we cannot forget the urgent need to improve care for those people living with dementia. Dementia care is a test of our values. I am sure that no one in this House believes that anyone should face this journey alone or without support. We should all be committed to building a fairer, more compassionate care system that delivers for all, including the people of Redditch and the villages.