data
Things have changed for the better. Is that the case for your neurological condition?
Sarah Joiner, Vice Chair of the MS Trust and member of The Neurological Alliance #MyNeuroSurvey Steering Group, writes: I was diagnosed with multiple sclerosis in 1981. Back then I received care from a consultant and a small medical team. Hours of waiting all morning, an examination to see how the condition had progressed, and some […]
Neurological Alliance: Collaboration is vital in implementing new Health and Social Care Data Strategy
The Neurological Alliance welcomes many of the commitments outlined in the Department of Health and Social Care’s draft data strategy published on 22nd June 2021. However, more needs to be done to ensure that people with neurological conditions and their support groups are directly involved in shaping these initiatives – we will be working with […]
