My Neuro Survey

[HelenPSPA]

Have you shared your experience of neuro services with The Neurological Alliance yet?

The information collected via #MyNeuroSurvey will be given to decision-makers to help bring out change.

Share your experience below 👇👇👇

facebook.com/.../a.11951898...

[Sk7lar7]

I haven’t had a confirmed diagnosis as yet although the private consultant thinks it is CBS following the MRI in March 2021. But I am now on cobenaldopa to eliminate Parkinson’s.I am now with King’s neuro and awaiting a DACT scan and a 2nd MRI

[HelenPSPA Administrator PSPA in reply to Sk7lar7]

Thank you for sharing. PSPA are available if you need to chat to anyone - you can get in touch at 0300 0110 122 or by emailing [e-mail]

[messier]

The links seems to be broken. Is there a link that is not on Facebook for those of us who don't use that.

[HelenPSPA Administrator PSPA in reply to messier]

Morning, here is the direct link to the Neurological Alliance web page about the survey: neural.org.uk/share-your-ex...