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.
Gloucestershire family take on 100-mile RideLondon-Surrey challenge for Sue Ryder Leckhampton Court Hospice
A family are challenging themselves to complete a 100-mile cycle to raise money for their local Sue Ryder Leckhampton Hospice, who supported their wife and mother when she died.
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.
Alan Sutor took part in Sue Ryder's first Ride for Ryder cycling event in 1988 aged just 14. Fast-forward 31 years to the present day and he is preparing to take on the 2019 Ride for Ryder. He tells us why.
Anne, a Research Nurse at our Sue Ryder Leckhampton Court Hospice, battled sub-zero training runs to take part in the Brighton Marathon and raise over £1,500 to be there when it really matters. Here she talks about her #TeamIncredible experience.
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 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.
We were delighted to welcome our regular blogger, Richard Littledale, as keynote speaker at the Sue Ryder annual lecture last week. The event was hosted by Rachel Reeves MP at the House of Commons and discussed the topic of bereavement.