News and blog

Latest news and blogs from Sue Ryder.

For journalist or media enquiries, please contact our press office.

Image of a Sue Ryder male Healthcare Assistant with a neurological resident at The Chantry

Demand for neurology plan following largest patient survey

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.

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.

Photo of the Scottish Government’s Minister for Public Health, Joe FitzPatrick MSP, visited Sue Ryder Dee View Court

Scotland’s neurological action plan: maintaining momentum

At the end of last year, the Scottish Government produced the country’s first national action plan on neurological conditions. But, now it’s been created, next comes the most crucial step: its delivery. Sue Ryder's Policy and Public Affairs Manager for Scotland Elinor Jayne, who helped shape the plan, reports.

Michelle Vann on her wedding day with her late mum Janis

“Manorlands staff move heaven and earth to make sure patients and their families feel safe, cared for and at home.”

Our Sue Ryder Manorlands Hospice provided Michelle Vann’s parents, Janis and Mark Lawson, with outreach nursing and respite care before they ended their lives at the hospice. This is their family’s story in Michelle’s own words.

Image of Sue Ryder logo

Sue Ryder comments on latest delay to adult social care green paper

The government has confirmed today that the Green Paper on adult social care has been further delayed and won't be published until next year.

Joe FitzPatrick MSP exploring the virtual jungle pursued by gorillas

MSPs try our virtual reality therapy in the Scottish Parliament

Following a successful pilot with residents at Sue Ryder Dee View Court, we are now rolling out the use of virtual reality as a form of mood-boosting therapy across all of our neurological care centres.

Bereavement support in Scotland - a report by Hospice UK and Sue Ryder

People struggling with bereavement unable to get support in Scotland

Bereaved people in Scotland are not receiving the support they need, according to new research commissioned by Sue Ryder and Hospice UK.