I've had trigeminal neuralgia since 2015 when I was diagnosed. It's become a bit more prominent and a problem in my life since my MS diagnosis. I was previously on tegretol (carbamazapine) for a period of time, unfortunately that stopped working even when increasing. I was then given the option of a nerve block every 8-10 weeks, longer as long as it wasn't needed. I've been having them now for the past year and a half, maybe longer and they have worked for me. Saved me if anything. I found out this week that my neurologist was told he was no longer able to run this clinic. So now I am dealing with unmanaged trigeminal pain and I have a 4 month old son. I'm also just about over a relapse too (which I've not heard from) - pals don't seem to be helping. This is more of a vent if anything because I'm in constant pain every day, I cry most of the time now because of it. It's destroying me. I do not know what to do as I've been provided with no alternative, I've been left. Oh and I had to find this information out myself about the clinic being stopped, no one was going to tell me. :/