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I'm courious also about the correlation between lesions and sx. I only have 2 small lesions. I have sx all the time, lead legs, TN, the hug, pain in my hands, slow digestion, foot pain. My neuro doesn't understand why I have the pain I do, I guess, because it doesn't correlate to my lesions.
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Not everything is related to MS. There could be something else entirely going on that's causing your pain. I have to remind myself not to blame everything on MS. It's hard not to.....because 9 times out of 10 it is because of MS. :rolleyes: But there's always that time it's not.
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Hi all-
I have read much of this thread. I do not have MS, but I do have chronic pain from a spinal cord injury two and a half years ago. I recently started on LDN, and am on 1.5mg per night now (started at 0.5mg one week ago). I'm working up to 3mg, or even 4.5, depending on how I feel. I just wanted to say hi and introduce myself. :) Libby |
Hi Libby and welcome to NT! Glad to hear you're trying LDN. Once you work your way up in dose I hope you can report some positive feedback from it. I've been taking it for a couple of years for MS. It's helped considerably with symptom management for me.
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Watch This Video!!
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And yet another interesting study reported recently.....A very interesting and informative read!!
http://beforeitsnews.com/story/1051/...altrexone.html |
I know LDN sometimes causes you to dream vividly. But I've been taking it for a few years now and I still get the most ridiculously vivid and sometimes disturbing dreams. They seem so real.....and I remember them clearly and think about them all day. Almost like they really happened.
Had another one early this morning. This time it was about my DH who passed away 10 years ago. It was so real. Just like he was right here. Really makes me feel strange. Anybody else have these dreams? Most of the time they don't bother me but sometimes they really shake me up. |
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anyone here take copaxone and LDN together?
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