News and blog

Latest news and blogs from Sue Ryder.

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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.

Miki Mitchell whose husband was cared for by Manorlands and the Queensbury Queens of the Mountain cycling club

“Dust off your bike and join us so that Manorlands can be there for more people like Chris.”

When she lost her husband Chris to cancer last October, Miki Mitchell was devastated. However, through it all, our Sue Ryder Manorlands Hospice was there to provide support and now, one year on, Miki is supporting them – bringing with her 100 entrants to Manorlands’ annual Bronte Sportive cycling event.    

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.

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Sue Ryder comments on latest delay to adult social care green paper

The government has confirmed today that the Green Paper on adult social care has been further delayed and won't be published until next year.

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.