Looking for recommendations for neurologist/neuromuscular physician in NJ or will travel to ends of earth for doctor for my cousin Robert Anderson. I'm a physician assistant, I am researching and researching. While I'm not dismissing the diagnosis of MMN, I think he requires a new set of eyes to evaluate him. He has a significant medical history treated for NHL which included chemo, radiation AND intrathecal chemotherapy. Any recommendations would be greatly appreciated.