Hi guys, sorry not been on, not feeling special, but have tried to drag my sorry botty back onto computer and do something and stop feeling sorry for myself. Still feeling and grieving for my lovely mum i lost recently.
Anyway had a copy of the letter from my Neurologist to the pain clinic which i finally have an appointment for in June. He is mentioning perhaps Lidocaine Patches.
I have asked a few MS friends and no one has been offered them, i please they are some sort of blocker.
Anyone on them would be interested in any feedback. Not sure i like the way they read lol.