“I have nothing but praise for Sue Ryder Neurological Care Centre Lancashire. Without them, I am sure that I would still be bed ridden”
Barry Whaite was admitted to Sue Ryder Neurological Care Centre Lancashire in April 2020, his head the only part of his body he could move independently. Barry spent all of the first national lockdown undergoing physiotherapy and rehabilitation, but in August 2020, he left the centre, walking again with help from a walking aid.
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.
Jean Piper’s husband Clive was cared for at Sue Ryder Wheatfields Hospice eleven years ago and Jean embarked on the ‘Dive for Clive’ skydive in his memory. Even when she herself was diagnosed with leukaemia she continued fundraising and volunteering in the Wheatfields shop, and it is that determination which saw her presented with the Sue Ryder Incredible Colleagues Award for Overcoming Obstacles last year.
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.
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.
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.
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.
“Initially, I thought no one could help me as no one could change what happened, but I’ve discovered that that isn't really the point of counselling at all.” Blogger Jess reflects on how, five years after her Dad’s death, counselling and therapy have helped her come to terms with her loss.