Sue Ryder Duchess of Kent Hospice's Lymphoedema team are donning odd socks to mark Lymphoedema Awareness Week (2-8 March), shining a light on the condition and showing support for those who have to wear compression garments to manage their symptoms from day-to-day.
During Lymphoedema Awareness Week, we meet Jan Bell, a Lymphoedema Therapist at Sue Ryder Duchess of Kent Hospice. Jan is a qualified nurse and has worked at the hospice for 23 years. The Lyphoedema service provides specialist care and support to help people manage their symptoms. In this blog, she talks us through a day in her life.
The support group held a Christmas party on Thursday 12th December, with lots of carol singing and a chance to talk to other carers, at Sue Ryder St John’s Hospice.
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.
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.
Carers’ Thursday, a support group for carers run by staff and volunteers from Sue Ryder St John’s Hospice and Carers in Bedfordshire, has just marked its second anniversary with a special celebration.
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.
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.