Visiting a Sue Ryder hospice or neurological centre remains significantly limited and continues to be carefully managed to ensure the safety of the people in our care, our staff and visitors.
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 is Human Rights Day, a day that celebrates the adoption of the Universal Declaration of Human Rights in 1948. In her latest blog, our Human Rights Lead, Jacqui Graves, explains how we are asking party leaders to commit to protecting human rights in the UK.
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, on Carers Rights Day, our Human Rights Lead Jacqui Graves highlights the rights of carers looking after people with life-limiting conditions and how they can ensure their rights are respected and protected.
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.