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.
When someone is diagnosed with a terminal illness, how do you break the news to them and their family? Dr Paul Perkins, Chief Medical Director, explains in his blog that there are no right or wrong answers, and it's the human connection which counts.
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.
Our Events Fundraiser Rachel has one of the hardest jobs in our events team: choosing who does – and (sob!) doesn’t – make it onto Sue Ryder's London Marathon team. Here, she explains how the process works and what you can do to be successful when you apply.
Whilst Brits know how they would spend their last days on earth, few are preparing for them, our new survey has revealed. As a result of this, we are calling on the nation to start talking about death.
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.
Yesterday’s Daily Telegraph reported that, according to NHS nurses, too many patients are being subjected to Do Not Attempt Resuscitation (DNAR) orders without families being told. Our Human Rights Lead Jacqui Graves provides the important clinical context behind the headlines.
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.