“I know that every mile I run and every pound I raise will be special.” Hayley Maud to run Leeds Half Marathon in memory of her father and to support Wheatfields Hospice
Hayley Maud is set to take on the Asda Foundation Leeds Half Marathon on Sunday 10 May in memory of her father, Andy, and to raise vital funds for Sue Ryder Wheatfields Hospice in Leeds, whose Community Team cared for Andy at home in 2019.
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.
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.
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.
As part of our summer appeal, Val Lunn recounts how, in the space of a year, she lost her husband and son – and how Sue Ryder supported her family through the toughest time of her life.
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.
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 report, 'Time to get it right', published today, gives a detailed 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.
“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.
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.