Oldham MP demands Government makes dementia a priority

DEBBIE Abrahams MP  has joined forces with Dame Arlene Phillips, Vicky McClure and Alzheimer’s Society to demand Government make dementia a priority 

The Saddleworth West and Lees MP, Chair of the All Party Parliamentary Group on Dementia, joined Alzheimer’s Society Ambassadors, Vicky McClure and Dame Arlene Phillips, as well as Elliot Colburn MP and Ananga Moonesinghe, who lives with dementia, in delivering an open letter to Prime Minister Rishi Sunak at Downing Street, demanding the Government urgently fulfil their promises on dementia.

Launched by leading dementia charity Alzheimer’s Society, the open letter has been signed by over 36,000 members of the public and famous names including Choreographer Dame Arlene Philips and actor Vicky McClure and urges Rishi Sunak to deliver on previous Conservative Party commitments on dementia and not let the UK’s biggest killer fall down the political agenda.

(L-R)  Dame Arlene Phillips, Vicky McClure, Ananga Moonesinghe (living with dementia), Alzheimer’s Society CEO Kate Lee, Debbie Abrahams MP and Elliot Colburn MP, handing in a public letter to Rishi Sunak at Downing Street urging him to prioritise people affected by dementia. Picture date: 19 Jan 2023. Photo credit should read: Jeff Moore.
(L-R) Dame Arlene Phillips, Vicky McClure, Ananga Moonesinghe (living with dementia), Alzheimer’s Society CEO Kate Lee, Debbie Abrahams MP and Elliot Colburn MP, handing in a public letter to Rishi Sunak at Downing Street urging him to prioritise people affected by dementia. Picture date: 19 Jan 2023. Photo credit: Jeff Moore.

Debbie Abrahams, Oldham East and Saddleworth MP and Chair of the APPG on Dementia, said:

“Previous Conservative Prime Ministers have actively committed to improving the lives of people affected by dementia. Now Rishi Sunak must deliver on promises to reform social care, double dementia research funding and release a ten-year plan for dementia which gives the condition the priority it deserves.

The 36,000 people who signed the open letter are making themselves clear – they don’t just want to hear empty promises, they want to see action. People with dementia can’t and won’t wait any longer.”

With diagnosis rates still sitting below pre-pandemic levels, national figures reveal people are waiting up to two years in some areas for a diagnosis*. This means they will be missing out on vital treatment and support. Alzheimer’s Society research also shows three in five people affected by dementia struggled to get social care in the past year, with half of family carers revealing they ended up in crisis, such as rushing their loved one to A&E due to lack of support**.

The charity is concerned the deepening workforce crisis in social care – with vacancies sitting at 165,000*** – risks leaving people with dementia desperate for help while living costs soar. Alzheimer’s Society say it’s more important now than ever for the Government to prioritise dementia.

In the past year, the Government has made many commitments on dementia, promising to deliver a ‘visionary ten-year plan’ for dementia, to reform the social care system and double spending on dementia research by 2024.  Alzheimer’s Society says the delivery of these will be transformational for the lives of the 900,000 people living with dementia but calls on the Government to urgently make these a reality to prevent a deepening crisis in dementia care.

This follows the news last year that a new drug, lecanemab, was shown to slow cognitive decline in people living with Alzheimer’s disease. Unfortunately, this breakthrough will mean little if diagnosis rates remain stagnant and often inaccurate. This treatment works best for people with early Alzheimer’s disease. Without early and accurate diagnosis, we risk hopeful advancements like this having minimal effect.

Kate Lee, Alzheimer’s Society CEO, said:

“Dementia awareness and support has come a long way since the disease came into my family sixteen years ago – but there is still so much to do. Too many people still face dementia alone, and PM Rishi Sunak has the chance to seize this moment and genuinely transform dementia research, diagnosis, and care for one of the biggest health challenges in the UK.

“We’ve welcomed previous commitments from the Government, but we’re concerned they’re falling by the wayside. The recommitment to the National Dementia Mission – to double dementia research spend – was a promising step, but we’re yet to see tangible action, while progress on the ten-year plan on dementia has stalled and social care reform scrapped. When asked for an update, the Government have told us ‘in due course’ 25 times*, which isn’t good enough – sadly dementia doesn’t wait for ‘due course’. Quite simply dementia is not a priority.  

“We’re still in the middle of a tough winter, with one in seven people with dementia stopping or reducing their support services. Families have had to make impossible choices in the face of inadequate care from a broken social care system. But hope is on the horizon – we saw the first ever drug to slow down Alzheimer’s disease late last year, showing that this is a fight we can win. Our letter to the Prime Minister urges for change – a massive reform of social care, a visionary ten-year plan for dementia, and the National Dementia Mission funding to unlock treatments for people now and in the future.”

Ananga, who lives with dementia, 76, from Luton, said:

“I’ve travelled to the steps of Downing Street to send an important message to the Government – make dementia a priority. When I was diagnosed, in the two years under the care of the Memory Clinic I was only told I had dementia and given medication. I didn’t get enough support and had to find it all out on my own. Dementia is just as important as any other condition and the Government need to make good on their promises for people living with dementia now and in the future.”