Guest guest Posted July 22, 2003 Report Share Posted July 22, 2003 Hi Lin, I think it's a terrific idea.....just think, if LDN works for him, then he may cause the NMSS or MSAA to stand up and take notice.....But I doubt it.....there's no money in it. Just think about this....what would happen to the NMSS if there happened to be a cure???? Does out of work ring a bell...lol....I wouldn't look for that happening any time soon. We need to keep helping ourselves, and I think we are off to a good start with LDN. Hugs, Sally > I TOLD ONE OF THE GYE'S AT MSAA ABOUT LDN.HE IS GOING TO TRY IT. > HE HAS MS TOO.IT EVEN HAS EFECTED HIS SPEACH.HE'S MY PERR CONSELER > AND A VERY NICE GYE.HE COULDNT BELEAVE HOW CHEEP LDN IS.THE OTHER > DRUGS HE TAKES COST BIG BUCKS LIKE WE ALL KNOW. > I HOPE I DID A OK THING BY MENTONING LDN TO HIM. > TELL ME IF I WAS WRONG. > ALL TAKE CARE. LIN Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2003 Report Share Posted July 23, 2003 Hi Lin, It's okay to mention LDN to people. How they accept your advise is their problem. I have mentioned it to a lot of people. I think that most people have to have it proven to them first. Hey you are only trying to help them. I think that when people take LDN, they get that attitude that MS is NOT going to win. We feel good about ourselves because we are fighting this disease. I have had MS for 26 years and it wasn't until this year that I started to educate myself about it. Now I feel that I have power over it and I definetely have THE ATTITUDE.. I think that it takes a certain type of person to take LDN. It's a person that wants to get above the MS and get better. Some people are happy to sit back and listen to the doctors. I was that type of person until this year. I just didn't have the guts to go against the doctor. I am going to see my neuro in a couple of weeks. Will he be surprised when I tell him that I have gotten rid of copaxone and am taking LDN and DOING GOOD. Wishing you health. Marie ----- Original Message ----- From: " linriker " <mylinda63@...> <low dose naltrexone > Sent: Tuesday, July 22, 2003 4:14 PM Subject: [low dose naltrexone] talking msaa > I TOLD ONE OF THE GYE'S AT MSAA ABOUT LDN.HE IS GOING TO TRY IT. > HE HAS MS TOO.IT EVEN HAS EFECTED HIS SPEACH.HE'S MY PERR CONSELER > AND A VERY NICE GYE.HE COULDNT BELEAVE HOW CHEEP LDN IS.THE OTHER > DRUGS HE TAKES COST BIG BUCKS LIKE WE ALL KNOW. > I HOPE I DID A OK THING BY MENTONING LDN TO HIM. > TELL ME IF I WAS WRONG. > ALL TAKE CARE. LIN > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2003 Report Share Posted July 23, 2003 I recently saw my nuro and he was very supportive. He could see the improvement in my condition (after only about a month or so of LDN) and was impressed that I was no longer taking hordes of symptom suppressing drugs. About the only thing I now take is LDN. He even conferred with my GP about it. Both doctors are impressed with how well I am doing. My nuro also asked about the URL for Low Dose Naltrexone so he could get some info my source. I will be having a MRI next November, hopefully he will see enough improvement to be convinced to recommend LDN to others. Both doctors are impressed with my initiative to heal myself! Original Message: ----------------- From: Marie Deady Mardea@... Date: Wed, 23 Jul 2003 07:25:25 -0400 low dose naltrexone , mylinda63@... Subject: Re: [low dose naltrexone] talking msaa <html><body> <tt> Hi Lin,<BR> It's okay to mention LDN to people. How they accept your advise is their<BR> problem. I have mentioned it to a lot of people. I think that most people<BR> have to have it proven to them first. Hey you are only trying to help them.<BR> I think that when people take LDN, they get that attitude that MS is NOT<BR> going to win. We feel good about ourselves because we are fighting this<BR> disease. I have had MS for 26 years and it wasn't until this year that I<BR> started to educate myself about it. Now I feel that I have power over it<BR> and I definetely have THE ATTITUDE.. I think that it takes a certain type<BR> of person to take LDN. It's a person that wants to get above the MS and get<BR> better. Some people are happy to sit back and listen to the doctors. I was<BR> that type of person until this year. I just didn't have the guts to go<BR> against the doctor. I am going to see my neuro in a couple of weeks. Will<BR> he be surprised when I tell him that I have gotten rid of copaxone and am<BR> taking LDN and DOING GOOD. Wishing you health.<BR> Marie<BR> ----- Original Message ----- <BR> From: " linriker " <mylinda63@...><BR> <low dose naltrexone ><BR> Sent: Tuesday, July 22, 2003 4:14 PM<BR> Subject: [low dose naltrexone] talking msaa<BR> <BR> <BR> > I TOLD ONE OF THE GYE'S AT MSAA ABOUT LDN.HE IS GOING TO TRY IT.<BR> > HE HAS MS TOO.IT EVEN HAS EFECTED HIS SPEACH.HE'S MY PERR CONSELER<BR> > AND A VERY NICE GYE.HE COULDNT BELEAVE HOW CHEEP LDN IS.THE OTHER<BR> > DRUGS HE TAKES COST BIG BUCKS LIKE WE ALL KNOW.<BR> > I HOPE I DID A OK THING BY MENTONING LDN TO HIM.<BR> > TELL ME IF I WAS WRONG.<BR> > ALL TAKE CARE. LIN<BR> ><BR> ><BR> ><BR> > Quote Link to comment Share on other sites More sharing options...
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