Guest guest Posted November 24, 2004 Report Share Posted November 24, 2004 Hi Carol, I have progressive ms and started taking LDN on 7/8/03. Have had significant improvement with urinary urgency and frequency, improved leg strength from the first day. No further improvements and no progression. Regards, Tom ----- Original Message ----- From: sunynbrite56@... low dose naltrexone Sent: Wednesday, November 24, 2004 9:13 AM Subject: [low dose naltrexone] Progressive help Hi Everyone. First, I'd like to wish you all a Happy Thanksgiving Next ~ I have a question for anyone who has Progressive MS and is taking LDN. I'd like to know if LDN is helping, and in what ways. I have a friend who is asking for his brother in law. I only know what wonderful changes LDN continues to do for me, I am RRM. so I can't very well give him the right information. I'd appreciate any replies. Again, Happy Thanksgiving. We all have so much to be Thankful For God Bless Carol Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 24, 2004 Report Share Posted November 24, 2004 --- Carol I am Secondary Progresseve and have been on LDN for just about a year now. I have had great results, slow but great results! I have had MS for 10 years and it has always been progressive but in my latest MRI in September there were no new lesions! Steve In low dose naltrexone , sunynbrite56@a... wrote: > Hi Everyone. > First, I'd like to wish you all a Happy Thanksgiving > Next ~ I have a question for anyone who has Progressive MS and is taking > LDN. I'd like to know if LDN is helping, and in what ways. I have a friend > who is asking for his brother in law. I only know what wonderful changes > LDN continues to do for me, I am RRM. so I can't very well give him the right > information. I'd appreciate any replies. > Again, Happy Thanksgiving. We all have so much to be Thankful For > God Bless > Carol Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 24, 2004 Report Share Posted November 24, 2004 I have either SP or PP not sure, neither are docs. I have been on LDN since July 4th 2003 (almost 1 1/2yrs) Like Tom, my bladder is better, more energy, sleep alot better . My walking has not improved, but I am no worse, and that is the most important thing. Happy Thanksgiving to you Carol and to all the great supporters on this LDN site. We have much to be thankful for!!!!!! Kiki Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 24, 2004 Report Share Posted November 24, 2004 Your results may vary from others on LDN if you are PPMS or SPMS. or even RRMS! My friend (SPMS) has gone downhill fairly rapidly while on the 4.5 mgs one year now and myself (SPMS) have kinda held stable with a slight downward trend while on 3.0 mgs(also one year now) but then 4.5mgs was way to powerful for me. My brother (SPMS) is much the same as he was a year ago on 3.0mgs but then we all have had MS for over twenty years. I have another lady friend with PPMS that LDN does nothing for at all. Yet most with RRMS are doing fine to amazing. Really only by trying can you determine how you will respond. I also firmly believe that Suppliments play a very large roll in our health.I may be hanging in there only because of the very large amount of Vitamins and other things I take daily. Reg. -------Original Message------- From: low dose naltrexone Date: 11/24/04 07:14:46 low dose naltrexone Subject: [low dose naltrexone] Progressive help Hi Everyone. First, I'd like to wish you all a Happy Thanksgiving Next ~ I have a question for anyone who has Progressive MS and is taking LDN. I'd like to know if LDN is helping, and in what ways. I have a friend who is asking for his brother in law. I only know what wonderful changes LDN continues to do for me, I am RRM. so I can't very well give him the right information. I'd appreciate any replies. Again, Happy Thanksgiving. We all have so much to be Thankful For God Bless Carol Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 24, 2004 Report Share Posted November 24, 2004 Carol, For myself, being very progressed to begin with, the slightest improvements are welcome! I don't believe I have progressed. It is more difficult for me to transfer now than one year ago, but I blame this on lack of movement and not enough stretching. Not progression! Better bladder control, improved sleep, no L'hermettes (sp) sensations, and more energy are good. I have been on LDN for just over 1 year now. 4.5mg now. Time will tell! Marcie Quote Link to comment Share on other sites More sharing options...
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