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Has anyone tried LDN and then changed back to a conventional treatment?

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Old 12-20-2009, 11:47 AM #11
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Perfect explanation of what LDN is, Cherie. The sx reduction is a bonus......but a BIG bonus. I wish everyone could have it. Even if LDN stopped relieving my sx I would still take it because I know it has slowed the progression of my disease.
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Old 12-23-2009, 09:55 AM #12
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I took ldn for awhile and didn't get any lasting results from it, not good ones anyway.

I'm in the process of starting Copaxone again without the autoject this time. Hopefully, I won't get the severe site reactions I got last time.

I really don't like not taking any MS med. My neuro doesn't like it either of course.
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Old 12-23-2009, 09:12 PM #13
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Quote:
Originally Posted by joellelee2000 View Post
I really don't like not taking any MS med. My neuro doesn't like it either of course.
My neuro was pretty livid with my decision, but only we know what's best for us, and at least he was rational enough to acknowledge that point.
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Old 12-24-2009, 06:10 PM #14
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I haven't used it but my thought is that as with anything MS, some things might work for some of us but not for others, or so we think. Its just a tricky damn disease.
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