Meet Sue Ryder St John’s Family Support Team, a multi-disciplinary team who support people from diagnosis onwards, during life-limiting conditions, and we also offer bereavement support after a loved one has died.
“When living with a life-limiting condition, there is still life to be lived. And here at Sue Ryder St John’s Hospice our multi-disciplinary teams do all we can to make sure that life is fulfilling.” These are the words of Funmi Shitta-Bey, Physiotherapist and Day Therapy Lead at Sue Ryder St John’s Hospice in Bedfordshire, who tells us more about her role.
Staff at Sue Ryder Thorpe Hall Hospice have been trialling an innovative Wellbeing Café to support patients to live as fully and actively as possible with great success.
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.
“At the hospice, I was able to become Mum’s daughter again instead of her carer – and grant her final wish.”
Emma Rayner's mum Clarissa spent her last two weeks at our hospice in Peterborough. In this blog post and moving video montage, Emma shares her family’s story.
"What do you say to someone facing a life-changing diagnosis? I have no idea - but I'm a good listener and that helps."
Penny Fisher has volunteered as a befriender and bereavement supporter at Sue Ryder Thorpe Hall Hospice since 2008, following the death of her husband. Here, she tells us why she gives her time.
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.
“When I found out Dad had cancer, I worried about my graduation – and about my future beyond it. I thought of every single day ahead when he wouldn’t be there,” writes Jess Bacon, whose dad died at our Thorpe Hall Hospice five years ago. Here, she recalls all the (dreaded) milestones that have come and gone since then.