Yes, Sally, I do have a verrrrrry supportive husband, and family as well. That helps a lot. My sister fiddled with her shifts at work and came on a day's notice when my lumbar puncture got unexpectedly cancelled and I had to reschedule on a day my husband was off. I am so so grateful for their support. ... and also thankful for everyone's support here, because as much as family tries, one thing they can't do is understand what it's like to have MS, to live MS.

Cherie, I'm actually not Canadian but close enough to the border! I have an appt with a supposedly LDN friendly neuro, my original, now ex-neuro is an unmentionable &^%$ and basically made it seem like he doesn't want me as a patient unless I got on a DMD, NOW. Tried to scare me by telling me of MS induced dementia cases. I need some time to think and he's not exactly helping.

Not sure about the Copaxone at this time, i think it makes sense to give the LDN a chance, I'm not so sure yet. Then I wonder if I should just play it safe and do both. I'm currently following the CCSVI work closely and would like to investigate treating that in the future.