My neuro is quite happy to chat and tell me what advances are being made into MS. He pretty much writes whatever prescription I ask him to (which is usually only for Ty, a low dose of an antidepressant, and an occasional sleeping tablet to take on the nights when my brain doesn't switch off or my legs/feet won't stop burning. There is no longer any examination, but he does interpret my MRI results.

Then he charges me 5 times what my GP charges.

Lyn