News and blog

Latest news and blogs from Sue Ryder.

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

The lymphoedema team at Sue Ryder Duchess of Kent Hospice in their odd socks.

Sue Ryder Duchess of Kent staff rock odd socks for Lymphoedema Awareness Week

Sue Ryder Duchess of Kent Hospice's Lymphoedema team are donning odd socks to mark Lymphoedema Awareness Week (2-8 March), shining a light on the condition and showing support for those who have to wear compression garments to manage their symptoms from day-to-day.

Jan Bell - Lymphoedema Therapist at Sue Ryder Duchess of Kent Hospice

A day in the life - Jan Bell, Lymphoedema Therapist at Sue Ryder Duchess of Kent Hospice

During Lymphoedema Awareness Week, we meet Jan Bell, a Lymphoedema Therapist at Sue Ryder Duchess of Kent Hospice. Jan is a qualified nurse and has worked at the hospice for 23 years. The Lyphoedema service provides specialist care and support to help people manage their symptoms. In this blog, she talks us through a day in her life.

Lindsay O'Kane Running

Mum to run 5k every day this December in support of Sue Ryder St John's Hospice

For her third December Daily Dash, mum of two Lindsay O'Kane is taking on the challenge of running 5km every single day throughout December, including Christmas Day, in support of Sue Ryder St John’s, who cared for her grandmother.

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.

A mum and a baby meet older homecare patients at an intergenerational afternoon tea

Sue Ryder Homecare Stirling brings generations together to encourage physical activity

Sue Ryder Homecare Stirling held an afternoon tea on Tuesday to bring together its service users, carers and their children to promote physical activity and intergenerational relationships.

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.

Our useful guide can help you answer lots of tough questions

Why don't we talk about death?

It’s a tough question that Sue Ryder are trying to tackle. Our latest marketing campaign has been launched to encourage people to start the conversation about death, and to cement our position as experts in this area.

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.

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.