Sue Ryder Neurological Care Centre The Chantry hosts its first conference for health and social care professionals
Sue Ryder The Chantry will be hosting its first conference for health and social care professionals on April 30th at Trinity Park in Ipswich. 'Establishing Effective Neurorehabilitation Services' will bring together a number of experts in the field of Neurorehabilitation to speak on relevant topics.
Recently, healthcare professionals attended the first Palliative Care Seminar at Sue Ryder Thorpe Hall Hospice, to discuss their specialist palliative care, future plans and partnership working.
Sue Ryder's Specialist Neurological Care Centre, The Chantry, had a recent visit from MP for Ipswich, Sandy Martin, who discussed the centre's crucial role providing care in the local area and the upcoming expansion of this key service.
“Running teaches us to keep moving forward, one step at a time – especially in our most painful moments.” These are the words of Sarah Riley who, five months ago, lost her dad to cancer. Since then, she has been fundraising in his memory and is taking on the London Marathon 2020.
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.
Pets can be a great support during illness and beyond – as volunteer Barry discovered when, following his wife Sarita’s death, he signed up their puppy Bella to become a certified Pets as Therapy dog.
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.
Over 15,000 people with neurological conditions are being placed in nursing homes for the elderly, our shocking report reveals
Our new report, 'Time to get it right' published today, gives a comprehensive picture on how people with neurological conditions such as motor neurone disease, Parkinson’s disease, multiple sclerosis, Huntington’s disease and acquired brain injury are being let down by health and social services in England.
“When I found out Dad had cancer, I worried about my graduation – and about my future beyond it. I thought of every single day ahead when he wouldn’t be there,” writes Jess Bacon, whose dad died at our Thorpe Hall Hospice five years ago. Here, she recalls all the (dreaded) milestones that have come and gone since then.
It’s a tough question that Sue Ryder are trying to tackle. Our latest marketing campaign has been launched to encourage people to start the conversation about death, and to cement our position as experts in this area.
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