News and blog

Latest news and blogs from Sue Ryder.

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

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.

Two people holding hands

Sue Ryder survey reveals almost half of people experience poor mental health following the death of a loved one

In response to the survey commissioned by Sue Ryder, we are launching our #JustSaySomething campaign in a bid to encourage everyone to open up about grief and bereavement, enabling a more honest, supportive grieving process for those affected and people supporting them.

National Grief Awareness Week Logo - A Heart with Two Hands

National Grief Awareness Week: Let's open up to grief

This week sees the UK’s first ever National Grief Awareness Week, encouraging us all to #OpenUpToGrief and break the taboo around death and bereavement, for a more open discussion of a subject which affects us all at some time in our lives.

Grace Woodward - Sur Ryder's new Retail Ambassador

Grace Woodward appointed as Retail Ambassador for Sue Ryder

Sue Ryder has recently appointed fashion stylist and consultant Grace Woodward as Retail Ambassador to advise on its sustainable fashion and clothing offer for its national retail network.

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.

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.

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 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.