News and blog

Latest news and blogs from Sue Ryder.

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

A nurse and patient holding hands

'You as a human being can make a difference' Breaking the news of a terminal illness

When someone is diagnosed with a terminal illness, how do you break the news to them and their family? Dr Paul Perkins, Chief Medical Director, explains in his blog that there are no right or wrong answers, and it's the human connection which counts.

Image of Sue Ryder logo

Sue Ryder responds to Boris Johnson's £25m cash boost for hospice services

Today (20th August 2019), Boris Johnson has secured a £25 million cash boost for hospice services. The Prime Minister said he's hopes the money 'alleviates the everyday pressure' faced by the sector. 

7 in 10 people haven't discussed their death with loved ones infographic

Silence is deadly: stigma attached to 'the D-word' means Brits are missing out on a better death

Whilst Brits know how they would spend their last days on earth, few are preparing for them, our new survey has revealed. As a result of this, we are calling on the nation to start talking about death.

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.

Miki Mitchell whose husband was cared for by Manorlands and the Queensbury Queens of the Mountain cycling club

“Dust off your bike and join us so that Manorlands can be there for more people like Chris.”

When she lost her husband Chris to cancer last October, Miki Mitchell was devastated. However, through it all, our Sue Ryder Manorlands Hospice was there to provide support and now, one year on, Miki is supporting them – bringing with her 100 entrants to Manorlands’ annual Bronte Sportive cycling event.    

Leckhampton Court Hospice at Home Lead Emma Wright speaks to a patient

“We go in and we let families be families again.”

“We bring hospice care into people’s homes – and it’s a true privilege.” Emma Wright of Sue Ryder Leckhampton Court Hospice’s Hospice at Home team gives us an insight into what her job involves as part of our summer appeal.

The Lunn family

“My experience of Sue Ryder’s care has taken away my fear of dying.”

As part of our summer appeal, Val Lunn recounts how, in the space of a year, she lost her husband and son – and how Sue Ryder supported her family through the toughest time of her life.

A girl wrapped in a blanket browsing the Online Community on her tablet 546

Bereavement benefit must change to better support those left behind

Sue Ryder is calling on the Government to better support those who have been bereaved as many are missing out on vital benefits and face falling into debt to pay for basic funeral packages.

Danielle Gill with her mum and sister

“I will be imagining Mum is waiting for me at the end of the 26.2 miles.”

Our Wheatfields Hospice at Home team cared for Danielle Gill’s mum Jean nine years ago. This year, she is taking on the London Marathon for Sue Ryder to say thank you. This is Danielle’s story in her own words.

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.

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