Guest guest Posted February 19, 2006 Report Share Posted February 19, 2006 nn, So good to hear from you. I've had MS since 1983, walk with a cane, sleep 16 hrs./day on Copaxone 2 yrs. I read the book, " Up The Creek With A Paddle " , excellent- talking about her husband's success w/ LDN. I called Copaxone (medical advisor) and my son is an M.D. Both said no problem with LDN at 4.5 mgs.--kind of a double insurance against MS progressing. I would not wait until your MS progresses to take LDN. I wish I would have known about it a long time ago. If your neuro does not prescribe (as mine would not) find another M.D. (G. P. or someone). Neuro's don't want to know anything about LDN-mine would not even return my phone call OR read anything. No money in it for them. Take care. Pat Gove >From: " nn Covert " <jcovert@...> ><pgove5@...> >Subject: ldn >Date: Sat, 18 Feb 2006 18:48:31 -0500 > >hi Pat, > I just read your post on the low dose naltrexone . I'm >debating taking LDN, I have been on Copaxone for 2 years also. While on >copaxone I haven't had any new symptoms but my old one just gets worse. I >have a limp on my right side where if I get really hot, really cold or very >nervous it really stiffens up and it's very hard to walk. I have talked to >my Nero and my family MD and they will not prescribe ldn for me. I'm know >perusing a phone consultation with Dr. Sullivan. I live in upstate NY and I >just wish I was completely 100% sure on taking ldn. If I could ask what >made you sure? I scared of ms and I am not doing well excepting I have it. >The group and posts are making stronger in excepting ms and I hope that >when I attend the LDN conference that it will help. Thanks for reading this >I hope you are doing well nn jcovert1@... Quote Link to comment Share on other sites More sharing options...
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