Un site LDN en francais : http://www.sep.over-blog.com

A board to discuss Low Dose Naltrexone (LDN) as a treatment for Multiple Sclerosis

Un site LDN en francais : http://www.sep.over-blog.com

Postby renaudjba » Sat Mar 19, 2005 10:41 am

Enfin un site LDN en francais : http://www.sep.over-blog.com
Fin de Màj 1 sept 2013

please to pardon the weak quality of my english. My native language is french. Nobody's perfect.

Please, let me know how many people are estimated to have LDN for MS.

Is it possible to know your sources?

THanks for your replies.

Last edited by renaudjba on Sun Sep 01, 2013 7:42 am, edited 1 time in total.
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Hi there...

Postby JoyceF » Sat Mar 19, 2005 11:11 am

Not sure if anyone can tell you just how many people are using the LDN but I'd guess probably thousands. I, myself, have been taking if for just about 3 years now and I think it has been somewhat of a miracle in my life. You might be wise to join the yahoo group that if affiliated with the www.ldninfo.org site. Just don't select single e-mails as you will be swamped. There is a lot of activity by LDN patients there. I get the daily digest which is one e-mail or so a day with all of the messages in it. I do believe that there are some members in France so it might be worth it to join and post a question there. Good luck to you and let me know if I can help you further. Oh and btw, your English is fine. It is much better then my French..*s*. JoyceF
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Postby PhireX » Sat Mar 19, 2005 6:47 pm

I would estimate about 3,000+ but that's just my guess.
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