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.
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.
Our Events Fundraiser Rachel has one of the hardest jobs in our events team: choosing who does – and (sob!) doesn’t – make it onto Sue Ryder's London Marathon team. Here, she explains how the process works and what you can do to be successful when you apply.
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.
“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.
Over 15,000 people with neurological conditions are being placed in nursing homes for the elderly, our shocking report reveals
Our report, 'Time to get it right', published today, gives a detailed 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.
Danny Gallagher has lived at our Sue Ryder Cuerden Hall Neurological Care Centre since January 2018. Here, his daughters Daniella and Gemma describe how he came to be at Cuerden Hall and the positive impact it has had on all of their lives.