News and blog

Latest news and blogs from Sue Ryder.

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

Image of Sue Ryder directions signage outside Sue Ryder Manorlands Hospice

Coronavirus (Covid-19) guidance: visiting a Sue Ryder hospice or neurological centre

Visiting a Sue Ryder hospice or neurological centre remains significantly limited and continues to be carefully managed to ensure the safety of the people in our care, our staff and visitors.

Jean Piper at the Incredible Colleagues Awards with Heidi Travis, in 2019.

Inspiring Wheatfields volunteer and fundraiser, Jean Piper, presented with special Sue Ryder award

Jean Piper’s husband Clive was cared for at Sue Ryder Wheatfields Hospice eleven years ago and Jean embarked on the ‘Dive for Clive’ skydive in his memory. Even when she herself was diagnosed with leukaemia she continued fundraising and volunteering in the Wheatfields shop, and it is that determination which saw her presented with the Sue Ryder Incredible Colleagues Award for Overcoming Obstacles last year.

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.

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.

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.

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.

Nelson Mandela's cell

Our responsibility on Global Human Rights Day

This Monday 10th December 2018 is the 70th anniversary of the adoption of the Universal Declaration of Human Rights. Lead Nurse in Palliative and End of Life Care Philip Ball reflects on how far we’ve come but warns that we mustn’t become complacent.

The Neurological Alliance Patient Experience Survey 2018

Making neurological services better – one survey at a time

If you or a loved one have experience of conditions such as multiple sclerosis, Huntington's disease, Parkinson's disease, brain injury or stroke, please complete the Neurological Alliance Patient Experience Survey.