Posted 8/6/2011 1:03 PM (GMT 0)
Hi neurogirl, I had the exact same symptom. Came on after about a year into treatment with an infectious disease dr. At that point he did a brain MRI and found lesions on my brain. Don't know if that is what is causing it but I then went on neurontin and haven't had it since. When I switched to LLMD she said she believed it was trigeminal neuralgia. It is very painful. My eye on the side of my face that was burning has been blurry off and on for years now which I believe is related. Are you treating with LLMD?