Guest guest Posted June 3, 2004 Report Share Posted June 3, 2004 I was diagnosed with MS eight years ago, at the age of 44. I have been taking BetaSeron for the past six years. I heard about LDN the other day from an aquaintance and would like to know more. She is using it, but combines it with Copaxone. I would like to know if that is common, or if it would be possible to switch entirely, dropping the BetaSeron, but I am a little nervous. I don't think that it is working as well as it used to, and the expense is a great hardship. If anyone can tell me more, I would appreciate it very much. I have relapsing remitting, but a good friend has chronic progressive and I am hoping to be able to pass on any information I get to her as well. Thanks Gail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 3, 2004 Report Share Posted June 3, 2004 Hi Gail, I have heard that you cannot take LDN with the interferons but you can with Copaxone. I personally was on Avonex but was so disatisfied with it that I dropped it. If you are not getting the results from BetaSeron that you used to, perhaps you should try something else for a while. If the something else doesn't work as well, go back to it. God Bless, Penny(the cheese) > I was diagnosed with MS eight years ago, at the age of 44. I have > been taking BetaSeron for the past six years. I heard about LDN the > other day from an aquaintance and would like to know more. She is > using it, but combines it with Copaxone. I would like to know if > that is common, or if it would be possible to switch entirely, > dropping the BetaSeron, but I am a little nervous. I don't think > that it is working as well as it used to, and the expense is a great > hardship. If anyone can tell me more, I would appreciate it very > much. I have relapsing remitting, but a good friend has chronic > progressive and I am hoping to be able to pass on any information I > get to her as well. Thanks > > Gail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 3, 2004 Report Share Posted June 3, 2004 I am sure there will be direct responses to your post. I would like to suggest taking a bit of time and going back through as many old posts as possible. You will find a wealth of information and many answers to your questions. Just " View all messages " and keep choosing previous. It is what I did, and found it not only helpful, but enlightening. I found answers to questions I had not yet thought to ask. Best Alan RRMS Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 11, 2004 Report Share Posted July 11, 2004 Alan, Thank you very much for your advice. I appreciate it and shall look into it soon, (several family crises here are interrupting my available PC time unfortunately). Go well and I wish you ever improving health, Gladys ----- Original Message ----- From: " alanms1579 " <alanms@...> <low dose naltrexone > Sent: Thursday, June 03, 2004 4:01 AM Subject: [low dose naltrexone] Re: LDn and MS > I am sure there will be direct responses to your post. I would like > to suggest taking a bit of time and going back through as many old > posts as possible. You will find a wealth of information and many > answers to your questions. > > Just " View all messages " and keep choosing previous. > > It is what I did, and found it not only helpful, but enlightening. I > found answers to questions I had not yet thought to ask. > > Best > Alan RRMS > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 16, 2004 Report Share Posted August 16, 2004 > > I would like to hear from some MS people who have experience with LDN. Many times, when I hear about something that sounds " too good to be true, " that turns out to be the case. > > Your replies directly to me would be fine, and would also be greatly appreciated. > > > > Wilmington, NC > > beme7627@y... =========== , Go to my LDN forum and read old and new posts, this should help. Low Dose Naltrexone Forum - Home http://ldn.proboards3.com/index.cgi? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 16, 2004 Report Share Posted August 16, 2004 Friday, I know that is what we are about. Since I just joined the group, I am trying to get caught up. I have only seen a few days of posts and a number of them were just about problems with neurologists. Several peopk,e have replied to me directly and I am most appreciative for the reinforcement. Friday <paraschick@...> wrote: thats what we are here doing . thousands of posts about exactly that - lnd n ms.> > I would like to hear from some MS people who have experience with LDN. Many times, when I hear about something that sounds "too good to be true," that turns out to be the case.> > Your replies directly to me would be fine, and would also be greatly appreciated.> > > > Wilmington, NC> > beme7627@y... Quote Link to comment Share on other sites More sharing options...
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