They are bringing out the big guns! Help me out

First of all I appolizes if this do not make sense as my cognitive function have been geatly affected. Can't follow recipes stuff like that whcih makes me feel very unconfident etc.
Anyway just saw my neuro. and had an MRI and it light up like a Christmas Tree.nearly half of my brain. I've been on Avvonex, Copaxone and they did not work....i've had 4 relapses this year alone. My use of the solumedral is so frequent its not nearly as effetice as before.

I have a hard time walking I have alot of wearkness and balance problems. Its gone too far they believe and so big guns means Tysabri.
Just waiting on my insurance to approve.

kind of freaked out yet kind of excited to feel like myself again, very active etc.
ANybondy know how long before its gets working? I'm not finding a lot on line. So ANY information would be helpful.
I've heard great things. It been back out now for a year and no PML reports.

Its just a hard time right now, my husband being my support though through this will not be too bad.
I'm not in too bad condition right?

If it doesn't work they have one more...chemo.

thank you
sorry if it doesn't make sense
Dana

Kimber, thank you for forwarding that thread of questions and answers. It was great. Sooo many links. I can't look at them all today is there a way to save this some how?

Hey Dana,

Wow, I am sorry!! You have had a really bad time!  Hang in there.  I don't have any advice I just wanted to offer my support.  I am really hoping the tysabri works for you.  I too, have heard great things about it.  It is supposed to be very effective.  You're remaining quite positive despite your tough year.  You are very inspiring.

Good luck and please keep posting.  I would like to know how you are doing.

Love and prayers,

have you asked about ldn?