I am about to enter my depressing time of the year: the appointment with the Neurologist. However I am interested in the disparity of treatments available around the country.
Is there anything izzy whizzy I should be asking about for PPMS? I am on nothing so far (except solifenacin)I was dx 2009 and I feel there should be something to repair/ slow down MS by now surely? They seem to be happy to manage the decline rather than take a more pro active approach. Bit sick of being told to be patient. Rant rant