Multiple Sclerosis

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June 27, 2023

Our response to the Major Conditions Strategy call for evidence

Today, The Neurological Alliance is submitting a response to the government’s call for evidence for the Major Conditions Strategy. The scope of the strategy as currently stated neglects to include hundreds of neurological conditions. Our response to the call for evidence addresses this. All members of the Alliance were invited to input into our response […]
December 15, 2021

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 […]
December 8, 2021

We have never needed patient advocacy and citizen advocacy more than we need it now

Caroline Clarke, CEO at the Royal Free London NHS Foundation Trust, writes: Thank you for giving me the opportunity to speak at your AGM and to restate what I said then to your members in this blog. I am the CEO at the Royal Free London NHS Foundation Trust, a group of hospitals in North […]