A while ago I moved to a different county to my neuro clinic. He was not my original neuro. He has never examined me but last year wrote to my gp and said I was slowly progressing
This years examination by phone as I admitted to having a few UTI,s he said I was having continuing progression
I have had MS for 20 years and felt quite ill and a bit disabled in the first 5 years, they were awful years He didn’t know me then as I was diagnosed in the county I live in now
I do not agree with his ideas about progression, Now my real question is I get a Sativex prescription from him. if I try and change to a neuro nearer to home would I still be able to get ?Sativex? I think probably not
Has anyone else been denied drugs they were on due to Postcode lottery when they moved?