The intense "electric" like pain jolts are back. They just explode with no rhythm or reason.
All I can think of is that my body has become adjusted to flexeril.
I have had almost none of these pains since the surgery on Dec. 19th 2014.
I honestly hate going to the neurologist who I've seen for years.
I have an appointment with a new one in may - how do i describe the pain so that he listens? do I actually ask if it's trigeminal neuralgia?
I guess you have to be your own advocate - I have made detailed noted from the time this started right after the bicycle accident in July 2008. What treatments, what medications......
We'll see...