Guest guest Posted December 2, 2005 Report Share Posted December 2, 2005 Hi , I found out about the ldn on the ldn website about three and a half years ago, It has been the best thing I ever did. Judi On Dec 2, 2005, at 1:29 PM, Fontenot wrote: > Wow! Judi has 3 yrs and Bren 2.5? How did you veterans first find > out about it? I know now that it's word of mouth. Any one on it > longer than 3 yrs? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2005 Report Share Posted December 3, 2005 --- In low dose naltrexone , Fontenot <kitefest5@y...> wrote: > > Wow! Judi has 3 yrs and Bren 2.5? How did you veterans first find out about it? I know now that it's word of mouth. Any one on it longer than 3 yrs? > ======== I read about LDN at GoodShape's forum 4 years before I decided to try it...A HUGE MISTAKE in waiting that 4 years to try LDN...like many I thought it was too good to be true. The real pioneers are Jeanie Zeis a few others who post at GoodShape's and GoodShape's wife(now deceased of other health problems besides MS). Jeanie's been on LDN I think more than 6 years...possibly 7 or 8 years. She has not had any progression of her chronic progressive MS since starting LDN. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2005 Report Share Posted December 3, 2005 I heard about it in October 2002 from Steve, who started it 3 weeks earlier. I started the next April, 961 days ago. http://www.larrygc.com/mystory [low dose naltrexone] Re: LDN Pioneers >> Wow! Judi has 3 yrs and Bren 2.5? How did you veterans first find out about it? I know now that it's word of mouth. Any one on it longer than 3 yrs?> ========I read about LDN at GoodShape's forum 4 years before I decided to try it...A HUGE MISTAKE in waiting that 4 years to try LDN...like many I thought it was too good to be true. The real pioneers are Jeanie Zeis a few others who post at GoodShape's and GoodShape's wife(now deceased of other health problems besides MS). Jeanie's been on LDN I think more than 6 years...possibly 7 or 8 years. She has not had any progression of her chronic progressive MS since starting LDN. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2005 Report Share Posted December 3, 2005 I am pleased to say that after 2.5 years, here in Italy we have no reasons to believe LDN stops working for MS. Also, 100% sure it has not side effects and wont hurt you. Look at the first messages in this group. You might find some old LDN users and their email starting posting in this group since 2002. Good Luck Max > > Wow! Judi has 3 yrs and Bren 2.5? How did you veterans first find out about it? I know now that it's word of mouth. Any one on it longer than 3 yrs? > > > --------------------------------- > DSL Something to write home about. Just $16.99/mo. or less > Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.