Meet Liz Maitland, Chaplain at Sue Ryder Manorlands Hospice. Liz has worked at the hospice for 11 years and provides spiritual support to patients, families, carers and staff. Here, she talks us through a day in her life.
Sue Ryder Manorlands Hospice has taken a pioneering digital approach to the way it delivers its day therapy service, to support patients dealing with life-limiting conditions at home during the coronavirus lockdown.
Big-hearted bucket collectors raise £100,000 for Sue Ryder Thorpe Hall hospice - Hospice Care Week 2019 stories
Come rain or shine, Sue and Pete Woolfitt have loyally held bucket collections for Sue Ryder Thorpe Hall Hospice for nearly a decade – raising an incredible £100,000. This Hospice Care week we'd like to say thank you for their amazing support.
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.
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.
"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 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.
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.