Welcome to the board!
I was on Tysabri until last September when my Neuro took me off of it because of the report that came out of Europe of 2 new people that had been found with PML. For me, it didn't seem to be doing anything anyway. It is mainly for people that have Relapsing Remitting and my Neuro diagnosed me with Primary Progressive MS in May of 2007 after first dx'ing me with RRMS in June of 2006. However, when talking to others that were on the Tysabri, they were very happy with it and it seemed to be doing them some good. I guess it would be a personal choice.
I am waiting to start a treatment of Cytoxin as soon as my Neurologist that I saw in Chicago emails his protocol to my Neuro here in Idaho Falls. I guess I am not really sure what LDN is so I can't really be of any help to you in that respect.
Hopefully you will find a home here on the board. There are a lot of good people helping everyone and the Forum Moderators here are really great! We all understand wht you are going through!
Good luck and God Bless You!
Chuck the old man :>)
AMWTP Training Instructor
Idaho Falls, Idaho
Diagnosed with PPMS May, 2006
but still working at the present.
Tried just about everything there is for MS, including Tysabri
Waiting to start Cytoxin Treatments soon.