Guest guest Posted June 23, 2008 Report Share Posted June 23, 2008 INGRID - my guess would be frequent testings!! how else would it be possible to know that ANYTHING has changed, healthwise!!?? marshiris@...Gas prices getting you down? Search AOL Autos for fuel-efficient used cars. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 23, 2008 Report Share Posted June 23, 2008 How soon will you know that LDN stops the progress in MS? Ingrid [low dose naltrexone] Re: LDN and MSResults. Everyone wants to see results (I hope you do).I saw positive results after two weeks. Fatigue lessened, blurry eyesight improved, better balance. It was quite amazing, I thought.A good 6-9 month trial is what you should give LDN before thinking it's not working.Art-->> Hello,> I have a MS for 4 years. I would like to know how long it takes before > results are seen? Thank you,> Svetlana>------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 23, 2008 Report Share Posted June 23, 2008 what dose do you take? From: Gunn Dybfest <gunn.ingrid@...>Subject: Re: [low dose naltrexone] Re: LDN and MSlow dose naltrexone Date: Monday, June 23, 2008, 1:46 PM How soon will you know that LDN stops the progress in MS? Ingrid [low dose naltrexone] Re: LDN and MSResults. Everyone wants to see results (I hope you do).I saw positive results after two weeks. Fatigue lessened, blurry eyesight improved, better balance. It was quite amazing, I thought.A good 6-9 month trial is what you should give LDN before thinking it's not working.Art-->> Hello,> I have a MS for 4 years. I would like to know how long it takes before > results are seen? Thank you,> Svetlana>------------ --------- --------- ------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 23, 2008 Report Share Posted June 23, 2008 How long is a piece of string? Gunn Dybfest wrote: > > How soon will you know that LDN stops the progress in MS? > > > > Ingrid Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 23, 2008 Report Share Posted June 23, 2008 That depends on the individual. For me it was after being on LDN for a few months. I realized I didn't desire IV Solumedrol and oral Prednisone, which I would request when I was going through an exacerbation. Some of my symptoms improved and some stayed the same, but none really got any worse. I have been on LDN since March 2005. Before that I was on a roller coaster using the FDA-approved MS meds, all without success and all with terrible side-effects. I'm still not sure what Avonex, Copaxone and Novantrone may have done to me long term. Same goes for the steroids. If I had been prescribed LDN in 1996 when I started having MS-related problems again I wouldn't have the handicaps (god, I hate using that term when referring to me) I now do. Art -- > > How soon will you know that LDN stops the progress in MS? > > Ingrid Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 23, 2008 Report Share Posted June 23, 2008 I take 4.5mgs every night. Art -- > > what dose do you take? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2008 Report Share Posted June 26, 2008 I just had to ask that question.... the text prior to it confused me a bit.... Ingrid Re: [low dose naltrexone] Re: LDN and MS INGRID - my guess would be frequent testings!! how else would it be possible to know that ANYTHING has changed, healthwise!!?? marshiris@... Gas prices getting you down? Search AOL Autos for fuel-efficient used cars. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2008 Report Share Posted July 8, 2008 Hello ALl. I have a MS and I take LDN 3.0 mg for 3 weeks. I don't have a siteeffects but I don't feel better too. No energy, the same spastisity and stiffness. Maybe I have to take LDN 4.5 mg. Does anyone have the same problems? Thank you, Svetlana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2008 Report Share Posted July 8, 2008 4.5mgs is considered the optimal adult dosage. Taking it is entirely up to you. Art -- > > I understand that 3 weeks is not enough but if I don't have any side effects maybe i can take 4.5mm? > > Thank you Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2008 Report Share Posted July 8, 2008 Thank you From: Art H. <rtee54@...>Subject: [low dose naltrexone] Re: LDN and MSlow dose naltrexone Date: Tuesday, July 8, 2008, 7:06 AM 4.5mgs is considered the optimal adult dosage. Taking it is entirely up to you.Art-->> I understand that 3 weeks is not enough but if I don't have any side effects maybe i can take 4.5mm?> > Thank you Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 22, 2008 Report Share Posted August 22, 2008 hi stephen,i do not really know how is the way to get these posts or articles,but there is a space on this forum/site where are reported all the patz.life experiences. there you will get the answers to your question. my best emiliano > > Hello Everybody > > Does anybody have any information on whether it is wise to start LDN > therapy during an exacerbation of MS? I read one neurologist - who > isn't totally dismissive of LDN's use in treating MS - say that he > would not recommend this. > > I'd be particularly interested to hear of people's real life > experiences with this. > > Thanks > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 22, 2008 Report Share Posted August 22, 2008 Thanks for that, Emiliano. I'll take a look at the LDN forum...Regards [low dose naltrexone] Re: LDN and MS hi stephen,i do not really know how is the way to get these posts or articles,but there is a space on this forum/site where are reported all the patz.life experiences. there you will get the answers to your question. my best emiliano > > Hello Everybody > > Does anybody have any information on whether it is wise to start LDN > therapy during an exacerbation of MS? I read one neurologist - who > isn't totally dismissive of LDN's use in treating MS - say that he > would not recommend this. > > I'd be particularly interested to hear of people's real life > experiences with this. > > Thanks > > > Send instant messages to your online friends http://uk.messenger. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 22, 2008 Report Share Posted August 22, 2008 When I switched from Copaxone to LDN, March 2005, I was going though an exacerbation. Not only stopped it, but started to reverse symptoms. Art -- > > Hello Everybody > > Does anybody have any information on whether it is wise to start LDN > therapy during an exacerbation of MS? I read one neurologist - who > isn't totally dismissive of LDN's use in treating MS - say that he > would not recommend this. > > I'd be particularly interested to hear of people's real life > experiences with this. > > Thanks > > > Quote Link to comment Share on other sites More sharing options...
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