Hi. I’m looking for anyone with the same problem as me.
For 6 years I’ve been taking amitryptiline for what was diagnosed as facial neuralgia.
Starting dose was 20mg and I was “instantly cured”. Over the last few years I have tried to reduce the dose but every time I do I end up going higher as the pain becomes worse and the original dose can’t cope. I feel like the medication acts as a “curtain” which blocks the pain.
Currently I take 100mg each night. I recently saw a neurologist and have had a CT scan plus an MRI & MRA All have come back clear.
I know stress makes it worse. Doctors are desperately trying to call it migraine but my symptoms don’t match. Pain only usually in the centre of my forehead. No light issues, no sickness and no visual disturbance.
I am at the end of my tether. I’ve suffered for 8 years in total and am now going to try changing my diet to remove caffeine initially and then other foods too.
Am I the only one????