Hi Brenda,

Welcome to NT. You've received some great advice already, and I second what Cherie said below, it makes a lot of sense if you plan to use LDN. I've been on Avonex, then Rebif, then Copaxone and finally, Tysabri. I sometimes think about what I'll do if I need to switch again, and for me it's a toss up between Avonex and Copaxone. I like the once a week shot, except for the fact it's a harpoon type of needle, lol.

I don't like to take a lot of meds, but the disease has made that decision for me. I try to reduce stress, eat well, exercise and get enough sleep and that helps too. Keep us posted on your decision.

I appreciate that Wiz. I too use no other medications - just the Avonex and I take two ibuprofen prior to the injection each week.

I am definitely leaning towards Copaxone and LDN...perhaps just LDN. Lot to think about.

My suggestion is to try the LDN for 6mos and see how you do, then, if you feel the need, add copaxone. I know a few on both and wouldn't give up either one, 'cause they dont know which one to give up..

I was on Copaxone for about a year and I still progressed rapidly to SPMS.. I haven't progressed in MS disabilirty since starting LDN 5.5 years ago.

It is great that you have taken charge of your care and I wish you well with whatever your choice of Med..