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.

Nursing Assistant Penny Jarvis

“My husband’s wish was to die at home. He wanted to be surrounded by his own things with his family and friends around him.”

Penny Jarvis’s husband Colin died in 2009, five years after he was first diagnosed with a rare degenerative brain disease. Penny was Colin’s main carer and he was able to die in his own home according to his wishes. Ten years on and Penny, a Nursing Assistant, now works as part of the Hospice at Home team at Sue Ryder South Oxfordshire Palliative Care Hub.

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.

Helen with her late mum

“Mum would be spurring me on if she was here, so I’m running a 5K and 10K in one day for her.”

39-year-old Helen Daniels is taking part in the Bedford Running Festival in September. She’ll be running in memory of her mum and to raise funds for the hospice that cared for her, Sue Ryder St John’s in Moggerhanger.

A panel comprising human rights experts (left to right) Tor Butler-Cole QC, Richard Harding, Sanchita Hosali and Jacqui Graves answered questions.

Our Human Rights in End of Life Care Conference: a retrospective

Sue Ryder hosted a free conference on human rights in end of life care on Thursday 27th June 2019 in London, exploring further how applying a human rights approach to practice can help deliver person-centred and compassionate care.

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.

Dee View Court Nurses discuss a patient

"No decision about me without me": why families must be involved in 'do not resuscitate' orders

Yesterday’s Daily Telegraph reported that, according to NHS nurses, too many patients are being subjected to Do Not Attempt Resuscitation (DNAR) orders without families being told. Our Human Rights Lead Jacqui Graves provides the important clinical context behind the headlines.

Sue Ryder Hospice at Home Nurse getting out of car

Sue Ryder South Oxfordshire Hospice at Home service cares for 310 patients in first year

The Sue Ryder South Oxfordshire Palliative Care Hub launched on Monday 9th April 2018 and, since then, Sue Ryder Nurses have provided palliative care for 310 local patients in their homes throughout the region.

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.