News and blog

Latest news and blogs from Sue Ryder.

For journalist or media enquiries, please contact our press office.

Image of a Sue Ryder male Healthcare Assistant with a neurological resident at The Chantry

Demand for neurology plan following largest patient survey

People with neurological conditions are facing long waiting times, limited access to specialists and say they are being discriminated against, a new survey by The Neurological Alliance has found.

A Sue Ryder The Chantry Neurological Care Centre resident painting

It’s time to get it right for people with neurological conditions in England

People with neurological conditions in England are being let down by the very health and care systems that are supposed to be supporting them – that’s the finding of our new report Time to get it right, writes our Policy and Public Affairs Manager (England) Duncan Lugton.

Chantry resident Simon is helped into bed using a chair lift

Over 15,000 people with neurological conditions are being placed in nursing homes for the elderly, our shocking report reveals

Our new report, 'Time to get it right' published today, gives a comprehensive picture on how people with neurological conditions such as motor neurone disease, Parkinson’s disease, multiple sclerosis, Huntington’s disease and acquired brain injury are being let down by health and social services in England.

Photo of Richard Littledale at Sue Ryder's annual lecture 2019

"Bereavement is a deep wound with no visible scar"

We were delighted to welcome our regular blogger, Richard Littledale, as keynote speaker at the Sue Ryder annual lecture last week. The event was hosted by Rachel Reeves MP at the House of Commons and discussed the topic of bereavement.

Mike rides into the distance

Mike's Vietnam to Cambodia Adventure

After seeing the difference that his wife makes every day as a palliative care nurse, Mike decided to cycle 400 kilometres from Vietnam to Cambodia to raise money for our Sue Ryder Leckhampton Court Hospice. Here he talks about his trip of a lifetime.

Photo of the Scottish Government’s Minister for Public Health, Joe FitzPatrick MSP, visited Sue Ryder Dee View Court

Scotland’s neurological action plan: maintaining momentum

At the end of last year, the Scottish Government produced the country’s first national action plan on neurological conditions. But, now it’s been created, next comes the most crucial step: its delivery. Sue Ryder's Policy and Public Affairs Manager for Scotland Elinor Jayne, who helped shape the plan, reports.

Jess Bacon and her dad

Why you should give bereavement counselling a try

“Initially, I thought no one could help me as no one could change what happened, but I’ve discovered that that isn't really the point of counselling at all.” Blogger Jess reflects on how, five years after her Dad’s death, counselling and therapy have helped her come to terms with her loss.

Joe FitzPatrick MSP exploring the virtual jungle pursued by gorillas

MSPs try our virtual reality therapy in the Scottish Parliament

Following a successful pilot with residents at Sue Ryder Dee View Court, we are now rolling out the use of virtual reality as a form of mood-boosting therapy across all of our neurological care centres.

Bereavement support in Scotland - a report by Hospice UK and Sue Ryder

People struggling with bereavement unable to get support in Scotland

Bereaved people in Scotland are not receiving the support they need, according to new research commissioned by Sue Ryder and Hospice UK.

Dee View Court neurological research team

Our research demonstrates economic value of proactive neurological care

Containing analysis carried out by independent experts, the report shows that proactive care early in someone’s life, such as self-management support and advice or respite care, can save in the region of 30–50% annually when compared to reactive care, i.e. when someone’s health requires urgent care.

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