“Running teaches us to keep moving forward, one step at a time – especially in our most painful moments.” These are the words of Sarah Riley who, five months ago, lost her dad to cancer. Since then, she has been fundraising in his memory and is taking on the London Marathon 2020.
Why our Sue Ryder Manorlands Hospice is pioneering hypnotherapy as a way for families to come to terms with bereavement
Our seven hospices routinely offer counselling to the bereaved and, in recent years, alternative therapies such as massage, reiki and reflexology – including, at our Sue Ryder Manorlands Hospice in West Yorkshire, hypnotherapy. For some who’ve experienced it, the results are transforming, as local blogger Stephen Whitehead discovered when he met Jacki Scholefield.
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.
Our Wheatfields Hospice at Home team cared for Danielle Gill’s mum Jean nine years ago. This year, she is taking on the London Marathon for Sue Ryder to say thank you. This is Danielle’s story in her own words.
"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.
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.
After Amy Goodacre’s mum Tracey died at Sue Ryder Thorpe Hall Hospice three years ago, she started fundraising so other families could experience the same expert care as hers did. In this blog post, Amy talks about her experience at the hospice and her latest venture – helping to organise our 2019 Walk to Remember event.
There are no available press releases