News and blog

Latest news and blogs from Sue Ryder.

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Kirsty with her mum Kathleen making a toast

“Mum and I didn’t know what Dad would have wanted for his funeral. Because of that, we talked about what Mum’s final wishes would be.”

Kirsty Hodgson’s mum Kathleen spent the last two weeks of her life at Sue Ryder Wheatfields Hospice in Leeds in August 2016. Here, she recounts their story and explains why they made plans were put in place for the end of her mum's life.

Valerie with her daughter Harriet

“Not all of us will have the opportunity to plan our death and I feel that, if you can, you should.”

Valerie Bevan, 69, was diagnosed with multiple sclerosis 26 years ago and now only has movement in her head and neck. She is a day patient at Sue Ryder Manorlands Hospice where her daughter Harriet works as a Community Fundraiser. This is her story in her own words.

Miki Mitchell whose husband was cared for by Manorlands and the Queensbury Queens of the Mountain cycling club

“Dust off your bike and join us so that Manorlands can be there for more people like Chris.”

When she lost her husband Chris to cancer last October, Miki Mitchell was devastated. However, through it all, our Sue Ryder Manorlands Hospice was there to provide support and now, one year on, Miki is supporting them – bringing with her 100 entrants to Manorlands’ annual Bronte Sportive cycling event.    

A girl wrapped in a blanket browsing the Online Community on her tablet 546

What to do if you struggle with days like Mother’s Day

"For those of us whose Mums have died, we are often at a loss as to how to deal with Mother's Day," acknowledges Christine Ellis, Head of Family Support at our Sue Ryder Wheatfields Hospice. "Do we ignore it? Do we feel sad or filled with regret? Do we celebrate it?" Chris, who has helped countless families through bereavement, shares her expert advice.

A Sue Ryder The Chantry Neurological Care Centre resident painting

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.

Chantry resident Simon is helped into bed using a chair lift

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.

Angie Lund and family

“I’ll be crying all the way to the finish line”: Angie’s London Marathon story

“Throughout the last few months of my beautiful mum-in-law Marian’s life, Sue Ryder Nurses were on call 24/7,” writes Angie Lund. “They ensured Marian's dignity remained intact, kept her totally pain free, gave us ongoing advice, and took her wishes about her care into consideration throughout. It is for this reason, in Marian’s memory, that I want to give something back by running the London Marathon.”

Dee View Court neurological research team

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.