Posted 3/15/2012 6:20 AM (GMT -5)
Yes when I started having some neurological problems, my ID dr. did a brain MRI. It revealed numerous lesions. However, neither the neurologist or the ID dr. had a clue. They indicate that it did not "look" like MS but they weren't sure and agreed it was "probably" from the lyme. I have to say it caused me great anguish but feeling wonderful now, I realize that many of us have these such things and never know about it. I do however think it is crucial to get proper treatment before they increase. My worse symptom that I think was from the brain lesions was the facial burning on one side of my face for which I continue to take a small dose of neurontin.