News and blog

Latest news and blogs from Sue Ryder.

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

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.

The lymphoedema team at Sue Ryder Duchess of Kent Hospice in their odd socks.

Sue Ryder Duchess of Kent staff rock odd socks for Lymphoedema Awareness Week

Sue Ryder Duchess of Kent Hospice's Lymphoedema team are donning odd socks to mark Lymphoedema Awareness Week (2-8 March), shining a light on the condition and showing support for those who have to wear compression garments to manage their symptoms from day-to-day.

Jan Bell - Lymphoedema Therapist at Sue Ryder Duchess of Kent Hospice

A day in the life - Jan Bell, Lymphoedema Therapist at Sue Ryder Duchess of Kent Hospice

During Lymphoedema Awareness Week, we meet Jan Bell, a Lymphoedema Therapist at Sue Ryder Duchess of Kent Hospice. Jan is a qualified nurse and has worked at the hospice for 23 years. The Lyphoedema service provides specialist care and support to help people manage their symptoms. In this blog, she talks us through a day in her life.

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.

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.

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.

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.