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.
We were delighted to welcome our regular blogger, Richard Littledale, as keynote speaker at the Sue Ryder annual lecture last week. The event was hosted by Rachel Reeves MP at the House of Commons and discussed the topic of bereavement.
At the end of last year, the Scottish Government produced the country’s first national action plan on neurological conditions. But, now it’s been created, next comes the most crucial step: its delivery. Sue Ryder's Policy and Public Affairs Manager for Scotland Elinor Jayne, who helped shape the plan, reports.
“Initially, I thought no one could help me as no one could change what happened, but I’ve discovered that that isn't really the point of counselling at all.” Blogger Jess reflects on how, five years after her Dad’s death, counselling and therapy have helped her come to terms with her loss.
Following a successful pilot with residents at Sue Ryder Dee View Court, we are now rolling out the use of virtual reality as a form of mood-boosting therapy across all of our neurological care centres.
Bereaved people in Scotland are not receiving the support they need, according to new research commissioned by Sue Ryder and Hospice UK.
Containing analysis carried out by independent experts, the report shows that proactive care early in someone’s life, such as self-management support and advice or respite care, can save in the region of 30–50% annually when compared to reactive care, i.e. when someone’s health requires urgent care.
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