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.
39-year-old Helen Daniels is taking part in the Bedford Running Festival in September. She’ll be running in memory of her mum and to raise funds for the hospice that cared for her, Sue Ryder St John’s in Moggerhanger.
Sue Ryder hosted a free conference on human rights in end of life care on Thursday 27th June 2019 in London, exploring further how applying a human rights approach to practice can help deliver person-centred and compassionate care.
Michael Durkin, 69, was supported by our Sue Ryder Thorpe Hall Hospice at Home team to care for both his mother, Kathleen, and his brother, Tom, at the end of their lives, keeping them at home.
“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.
That’s the question being asked by our Sue Ryder Thorpe Hall Hospice this International Nurses Day as we launch a recruitment drive to help deliver more care to more people in Peterborough.
"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.