National Occupational Therapy Week 2020: “We all work together to ensure the best outcome for the clients”
2-8 November is National Occupational Therapy Week. Here, Ashlie Meadows, Occupational Therapy Lead at Sue Ryder Neurological Care Centre The Chantry, talks about her passion for the work they do and its importance in helping those with a neurological condition.
“There are so many elements of my job that I love.” Fern, Sue Ryder Thorpe Hall Hospice's Inpatient Unit Manager
After a variety of other nursing environments and more than a decade on from her first placement at Sue Ryder Thorpe Hall Hospice, Fern is now their IPU Manager. She describes her nursing and managerial responsibilities, as well as the challenges and joys of working in palliative care.
“I started at Thorpe Hall in March and obviously things have been very different to how they would normally be.” Caroline, Sue Ryder Nurse
Arriving at Sue Ryder Thorpe Hall Hospice in March 2020, Caroline has had a long and varied career in nursing and brings a wealth of experience to Sue Ryder. But nothing could have prepared her for the impact Covid-19 would have on our healthcare system.
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.
For Year of the Nurse, where we celebrate the important work of our Sue Ryder Nurses, we begin by talking with Jacqui Ackroyd, who has been appointed St John's Hospice's new Developmental Ward Manager. “I am honoured to be a nurse and I am proud to work at Sue Ryder St John’s Hospice.”
“My husband’s wish was to die at home. He wanted to be surrounded by his own things with his family and friends around him.”
Penny Jarvis’s husband Colin died in 2009, five years after he was first diagnosed with a rare degenerative brain disease. Penny was Colin’s main carer and he was able to die in his own home according to his wishes. Ten years on and Penny, a Nursing Assistant, now works as part of the Hospice at Home team at Sue Ryder South Oxfordshire Palliative Care Hub.
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.
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.
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.