When someone is diagnosed with a terminal illness, how do you break the news to them and their family? Dr Paul Perkins, Chief Medical Director, explains in his blog that there are no right or wrong answers, and it's the human connection which counts.
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.
NICE guideline for end of life care: a major step change or well-intentioned but undeliverable at current levels of funding?
Today, Wednesday 16 October 2019, the National Institute for Health and Care Excellence (NICE) launch their new guideline for organising and delivering end of life care services for adults. Sue Ryder’s Policy and Public Affairs Officer Niamh Buckingham reports on the difference it could make to the people we care for
"My role is to empower people – and often it’s the smallest things that make the biggest difference."
Occupational Therapist Heather Bayliss shares how Sue Ryder Leckhampton Court’s multidisciplinary Day Hospice team supports people living with cancer, lung disease, heart failure or neurological conditions in Gloucestershire.
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.
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.
Staff at Sue Ryder Thorpe Hall Hospice have been trialling an innovative Wellbeing Café to support patients to live as fully and actively as possible with great success.
Jacqui Graves, Human Rights Lead at Sue Ryder shares her experience and learnings of implementing the training programme to date.
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.
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.