Visiting a Sue Ryder hospice or neurological centre remains significantly limited and continues to be carefully managed to ensure the safety of the people in our care, our staff and visitors.
“I know that every mile I run and every pound I raise will be special.” Hayley Maud to run Leeds Half Marathon in memory of her father and to support Wheatfields Hospice
Hayley Maud is set to take on the Asda Foundation Leeds Half Marathon on Sunday 10 May in memory of her father, Andy, and to raise vital funds for Sue Ryder Wheatfields Hospice in Leeds, whose Community Team cared for Andy at home in 2019.
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.
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.
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.
“It is so reassuring to know that Dad is being properly cared for by people who understand him and his needs.”
Tony has Huntington’s disease and has lived at our Sue Ryder Cuerden Hall Neurological Care Centre since 2014. Here, his daughter describes how he came to be at Cuerden Hall and the positive impact it has had on his and his family’s lives.
Earlier this month, we held our first engagement event ahead of the move from Cuerden Hall to our new Neurological Care Centre Lancashire.
“We bring hospice care into people’s homes – and it’s a true privilege.” Emma Wright of Sue Ryder Leckhampton Court Hospice’s Hospice at Home team gives us an insight into what her job involves as part of our summer appeal.
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.