On 5 October, Sue Ryder will be presenting at the Royal College of Nursing event, ‘What use are human rights in end of life care?’ to highlight the areas for development and discuss the changes that need to be made in order to embed a human rights approach to end of life care.
Sue Ryder has commented on extending bereavement benefits to unmarried partners with children, to help broaden access to these crucial bereavement benefits and make the process itself more flexible for those in need of this financial support.
Today (20th August 2019), Boris Johnson has secured a £25 million cash boost for hospice services. The Prime Minister said he's hopes the money 'alleviates the everyday pressure' faced by the sector.
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.
“We bring hospice care into people’s homes – and it’s a true privilege.” Emma Wright of Sue Ryder Leckhampton Court Hospice’s Hospice at Home team gives us an insight into what her job involves as part of our summer appeal.
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.
Sue Ryder is calling on the Government to better support those who have been bereaved as many are missing out on vital benefits and face falling into debt to pay for basic funeral packages.
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.