I know the dangers of researching medical conditions online (seem to always find the
bad stuff) so its nice to hear some
good stuff. I of course am worried about PML especially since I am currently on Prednisone & also revieved Rituxan less than 4 months ago. The reason I don't have clinical ms is because I have lung involvement, ms never leaves the CNS & never effects lungs. I have also met with a NMO specialist and while although quite similar to my disorder, still not it.