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.
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.
What happens when someone you love has died, leaving their belongings behind? How do you decide what to keep and – at what is such a painful time – work out which items ‘spark joy’? After watching the Tidying Up with Marie Kondo episode ‘Sparking Joy After A Loss’, Julia Cook reflects on losing her parents-in-law and how she navigated the difficult process of sorting through their effects.