News and blog

Latest news and blogs from Sue Ryder.

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

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.

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.

A carer sitting down with the person they are looking after at home

How can an understanding of human rights help carers?

Today, on Carers Rights Day, our Human Rights Lead Jacqui Graves highlights the rights of carers looking after people with life-limiting conditions and how they can ensure their rights are respected and protected.

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.

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.

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 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.