I had multiple lesions 2 in my brain and 7 or 8 in my spine. Diagnosed with MS. After 90 days Rocephin my MRI was almost clear you could barely see a couple on my spine. My MS specialist was amazed still won"t talk about
Lyme but told me to keep doing what I was doing because it was working.
I stayed on low dose Amoxy for a couple years decided to stop i felt great. Now I have a bunch of new lesions. They are tying hard to push Copaxone, I am almost considering it. But I am going back to Conneticut to see Dr.K and hopefully get more IV antibiotics. In my opinion the only way to really touch nuero Lyme.
MS and Lyme topic together sucks, in my opinion.