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Hi all,

I just joined. I've recently learned of LDN and am very excited and

hopeful about it. I was diagnosed with RRMS in 10/2000. That year

(6/2000 - 4/2001) I had 3 bouts of optic neuritis. Since then,

nothing until now.

Now I am having a MAJOR attack of spasticity, and had trouble

getting my doctor engaged. The doc pretty much pushed IV steroids

(I had 5 days of Solu-Medrol in fall 2000, and vowed NEVER AGAIN --

plus, the IV didn't get rid of the optic neuritis any faster than

the other two non-steroid-treated attacks). So I switched docs, and

have an appointment with the new one at the end of the month.

I was wondering if anyone can suggest arguments to help persuade my

new doc about LDN?

THANKS!

:)

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