Hi,

I have had MS for a 20 years, but it has not shown itself to be so bad until
now. I was diagnosed in 1997. I was not told it was MS in 1988 when I had
transverse mylitis.

I was doing fine up until I gave birth to my third daughter. I have
gradually gotten worse. I am currently on copaxone. It does not
seem to be working for me anymore. I cannot take avonex due to
serious side affects. I am considering tysabri.

Is there anyone out there taking this? I really need to know. You
see I am 42yrs old. I am trying to keep up with my three girls and I
I have to be there for them. I do the best I can, but I sometimes it
is hard. I have seen people doing well with tysabri, but not enough
people on this. What is your expeience? I am desperate to hear some
good feedback on this.

Thank You,

Mary Ann