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Bernadette's avatar

Presumably people with MS are undergoing a similar fate? Neurological services nationally have major resource shortfalls and have for years. Cinderella services & bottom of the pile sadly

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Sarah Tyler's avatar

I suppose it's something, which should be better than nothing. But when this 'service' is being transferred to the private sector, is that the slippery slope of the first of many?

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Miles Mandelson's avatar

When we reached the age of 70 we realised that living the dream in rural Cumbria could become a nightmare of needing to access limited health services scattered over a wide geographical area. So we decided to move back to Merseyside and felt vindicated in our decision when I became seriously ill and was able to access health care of the highest quality almost on our doorstep. I’m pleased that a solution of sorts has been found to reinstate neurology services in S Cumbria but, as others have intimated, it does feel like the thin edge of a wedge.

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M. Dowrick's avatar

A good friend in Exeter with a significant lung issue does not have access to a respiratory consultant because….there are not enough to go around. She is struggling.

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Shane Roche's avatar

You don’t always need a Neurologist to manage patients with Parkinson’s disease. I am a Geriatrician/General physician and have a special interest in Parkinson’s disease for over 25 years. I run a service in Westminster and Kensington and Chelsea for Parkinson’s patients. We need to make more use of specialists like me who are not neurologists.

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