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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.

Sue Ryder Homecare Stirling brings generations together to encourage physical activity
Sue Ryder Homecare Stirling held an afternoon tea on Tuesday to bring together its service users, carers and their children to promote physical activity and intergenerational relationships.

"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.

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.

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.

Our research demonstrates economic value of proactive neurological care
Containing analysis carried out by independent experts, the report shows that proactive care early in someone’s life, such as self-management support and advice or respite care, can save in the region of 30–50% annually when compared to reactive care, i.e. when someone’s health requires urgent care.