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

We understand that visiting loved ones is crucial to the health and wellbeing of all our patients and clients, and the safety of the people in our care remains of paramount importance.

An online community user on a tablet in their home

Our Online Bereavement Support - a lifeline during lockdown

The effects of the Covid-19 pandemic have transformed daily life for everyone, with the impact on many bereaved people being even more severe due to their isolation in lockdown and a sudden loss of face-to-face support from family, friends or counsellors. In such a difficult time, Sue Ryder's Online Bereavement Support services have provided a vital lifeline.

Occupational Therapist Heather Bayliss outside Sue Ryder Leckhampton Court Day Hospice

"My role is to empower people – and often it’s the smallest things that make the biggest difference."

Occupational Therapist Heather Bayliss shares how Sue Ryder Leckhampton Court’s multidisciplinary Day Hospice team supports people living with cancer, lung disease, heart failure or neurological conditions in Gloucestershire.

Jonathon, Richard and Simon Cox in their cycle helmets

Gloucestershire family take on 100-mile RideLondon-Surrey challenge for Sue Ryder Leckhampton Court Hospice

A family are challenging themselves to complete a 100-mile cycle to raise money for their local Sue Ryder Leckhampton Hospice, who supported their wife and mother when she died.

Cover of Postcards from the Land of Grief by Richard Littledale

Why I wrote 'Postcards from the Land of Grief': a book about bereavement

After Richard Littledale lost his beloved wife Fiona back in 2017, he decided to chronicle his experience of bereavement in the hope of comforting others. They have been turned into a book Postcards from the Land of Grief, published today, and 100% of the royalties will go directly towards Sue Ryder's expert and compassionate care.

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.

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.

Richard Littledale with his arm round his late wife Fiona

The muscle memory of grief

"People who have lost a limb sometimes experience the presence of the limb long after it has gone – as if the nervous system refuses to accept this new, altered reality. Just recently, I experienced a similar thing with my grief on two occasions." Blogger Richard Littledale opens up about times when he has turned to his late wife Fiona, only to find her no longer there. 

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 report, 'Time to get it right', published today, gives a detailed 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.