Guest guest Posted February 28, 2005 Report Share Posted February 28, 2005 Hello Bev, I think the address for the mesage board is low dose naltrexone Hope that helps - Jan [low dose naltrexone] Re: Re - Just curious To the left of the message board at is a place for permanent files, databases, links,Polls, etc. I'll try to copy it: Files Photos Links Database Polls Calendar Permanent info and posts can be put in the files and other appropriate sections. Not sure how. I'm sure some of you can figure it out. > Hi Jan, > Thanks for the kind words. However I am clueless as to how to implement the site stuff. Does anyone know who set up the message board for LDN on ? Maybe they would know how to create a stationary site for different areas of LDN. Does anyone out there know how this can be accomplished? > Thanks > Aletha Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 15, 2005 Report Share Posted July 15, 2005 Hi Aletha, My name is Christy. I have been taking LDN since October of 2004 (4.5mg). I have had marvelous results. I received my initial prescription from Dr. Ayers through a phone consultation. He's in Illinois, and alas I'm in GA. He no longer does the phone consulting. So far I have not been able to find any doctors in the entire state of GA that prescribe LDN. Are there any? I would love to find a Dr. within driving distance. Even if there isn't one, I could use the list so I can do another phone consultation. Thank you so much! Keep up the good work. Christy -----Original Message-----From: Aletha Wittmann [mailto:Aletha@...]Sent: Friday, February 25, 2005 5:38 PMlow dose naltrexone Subject: Re: [low dose naltrexone] Re - Just curious Hi , This group has such a wonderful response system. Many of my questions have been answered by others that have gone through similar problems. I have been accumulating a list of doctors that prescribe LDN and giving it out when ever any one is in need of it. Maybe others can do the same with lists of supplements etc. Perhaps also we can have a stationary list of supplements, other meds, side effects (and cures) etc. on the site, to help people out and to keep chatters from having to have to repeat the same info. I always wonder about what important topics I have missed in the past etc. Thanks Aletha Just curious........................My husband brought the mail in the other day and I received a invitation from the NMSS to attend a seminar on Tysabri, and guess who the speaker is............................my neuro!! Well this got me to thinking about his financial gain in trying to get me on this stuff, since he didn't even give me the time to look into LDN like I asked! Anyway, I'm just wondering if anyone knows how much $$ the pharmaceutical co. pay the Dr's. for every patient they get to take these type of drugs? Am I thinking negatively, or are these Dr's just padding there pockets at our expense?On a lighter note, I am biting the bullet and giving up on Rebif. I am so happy with what I am seeing/feeling with LDN I didn't want the Rebif to interfere. Thanks to all of you who encouraged me to give LDN a chance! Karin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 16, 2005 Report Share Posted July 16, 2005 Hi, Christy- I live in Woodstock GA, just an hour north of Atlanta. My neuro, who is in Marietta just prescribed LDN for me, and I just started two days ago. If you want her info, I am more than happy to give it to you. Just e-mail me directly, as I do not have her permission to put her name out publicly. Hope you are well. Take care, AmyChristy <christy147@...> wrote: Hi Aletha, My name is Christy. I have been taking LDN since October of 2004 (4.5mg). I have had marvelous results. I received my initial prescription from Dr. Ayers through a phone consultation. He's in Illinois, and alas I'm in GA. He no longer does the phone consulting. So far I have not been able to find any doctors in the entire state of GA that prescribe LDN. Are there any? I would love to find a Dr. within driving distance. Even if there isn't one, I could use the list so I can do another phone consultation. Thank you so much! Keep up the good work. Christy -----Original Message-----From: Aletha Wittmann [mailto:Aletha@...]Sent: Friday, February 25, 2005 5:38 PMlow dose naltrexone Subject: Re: [low dose naltrexone] Re - Just curious Hi , This group has such a wonderful response system. Many of my questions have been answered by others that have gone through similar problems. I have been accumulating a list of doctors that prescribe LDN and giving it out when ever any one is in need of it. Maybe others can do the same with lists of supplements etc. Perhaps also we can have a stationary list of supplements, other meds, side effects (and cures) etc. on the site, to help people out and to keep chatters from having to have to repeat the same info. I always wonder about what important topics I have missed in the past etc. Thanks Aletha Just curious........................My husband brought the mail in the other day and I received a invitation from the NMSS to attend a seminar on Tysabri, and guess who the speaker is............................my neuro!! Well this got me to thinking about his financial gain in trying to get me on this stuff, since he didn't even give me the time to look into LDN like I asked! Anyway, I'm just wondering if anyone knows how much $$ the pharmaceutical co. pay the Dr's. for every patient they get to take these type of drugs? Am I thinking negatively, or are these Dr's just padding there pockets at our expense?On a lighter note, I am biting the bullet and giving up on Rebif. I am so happy with what I am seeing/feeling with LDN I didn't want the Rebif to interfere. Thanks to all of you who encouraged me to give LDN a chance! Karin Start your day with - make it your home page Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 17, 2005 Report Share Posted July 17, 2005 can you tell me, please How to order it? Thank you Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 18, 2005 Report Share Posted July 18, 2005 > can you tell me, please How to order it? > Thank you ========= Medsmex in Mexico is a good source for ReVia brand Naltrexone. http://ldn.proboards3.com/index.cgi?action=display & board=links & thread=1105152047\ & page=1 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 18, 2005 Report Share Posted July 18, 2005 I agree totally. Don't forget the fact that the big pharmaceuticals ONLY want to make money. It doesn't matter how. Everything else isn't important. Killing, murdering: everything is allowed. The sick peoples are sick, so who matters (okee: we, but...) It is hard to believe, but it is the truth. Greetings, Simon (the Netherlands) >From: " rtee54 " <xltrt@...> >Reply-low dose naltrexone >low dose naltrexone >Subject: [low dose naltrexone] Re: Re - Just curious >Date: Mon, 18 Jul 2005 00:00:42 -0000 > > > > Good point, Dave Tayler. I would like to urge everyone crying out >for clinical trials o LDN to please stop!!! The drug has already had >clinical triels and was approved, and the only way to get it off the >market is to make it into an illegal drug and a controlled >substance. Then it can be conhtrolled and made inaccessible. > > > > I talked to the wife of a renown neurologist in Texas who had been >very infuential in the Ms Society at the national level. She told me >she quit promoting the MS Society when a really high mucky muck told >her (secretly) that no cure for any major disease would ever be found >again, using polio as the example. When polio was 'cured', it took >out part of the industry!!! Since then, I tell everyone to quit >walking for MS, etc. > > > > If there was a clinical trial for LDN, it would cost millions, be >made inaccesible, and then be 'approved' at a much higher cost to >cover the cost of the trials. THINK, people. A month's supply of it >now costs only about $20-30 a month. People with no insurance and on >Medicare can afford that now. They will not be able to if it goes >through clinbical trials. We don't need clinical trials now. The >anecdotal is enough for D.O.s and other doctors to prescribe it >without the trials. Neuros may not because it jeapordizes their >profession. It would empty their offices. > > > > That is a GOOD thing! > > > > Jan > > >-- >I must agree with the author of this post. It's legal and available. >We know about it and use it. We recommend it to those we think would >benefit. Why change things now? > >Artie > > _________________________________________________________________ Nieuw: Beeld en geluid met MSN Messenger 7.0 http://messenger.msn.nl/ Quote Link to comment Share on other sites More sharing options...
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