Hi. My GP has referred me to the neurologist. I think to reassure herself that my symptoms are compatible with my PA diagnosis. I can’t get too excited as it seems from reading here that the neuro may only have a basic knowledge of PA. But I may be lucky! How to best use this opportunity? What should I ask? Are there tests I should try to get? What can a neuro add to my care?!! Ideas please! Thank you so much. PS I have been SI for about a month now, alternate days as per BNF guidelines. My only ‘unusual’ symptom is that my bladder does not now let me know when it is full!
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