Page 1 of 1

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

Posted: Thu Apr 07, 2005 9:53 am
by renaudjba

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

Posted: Fri Apr 08, 2005 11:15 am
by Mary
Hello Jean-Baptiste

We've "connected"in another thread so you may know that LDN is the first and only drug I've taken for MS. I too was diagnosed after just one attack based on MRI results (August '04). I found out about LDN on the internet and took the info to my doctor who (somewhat reluctantly) prescribed it for me. The neuro is kinda ambivalent about what I do (although he was favouring Avonex) and he seems a little skeptical about LDN, but agreed to scheduled another MRI for August '05 which will give me six months on LDN. Based on the results of that MRI I will decide what to do next.

I haven't been on LDN long enough to offer much feedback. I feel no real outward effects from it and at this point I'm just trying to find the dosage that best suits me.

Hope that helps...

Aylish

Posted: Fri Apr 08, 2005 2:24 pm
by renaudjba

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

thanks for your reply. I dont think it will be enough for the neuros!!

Do not worry, I'll find what I need.

You do not tell me about your symptoms, neither about what LDN has changed in it ?

Hope you feel good.

Jean-Baptiste

Posted: Mon Apr 11, 2005 8:27 pm
by LarryLDN
This is my story from when I first started.. http://www.larrygc.com/mystory will take you there.

I'm coming up on 2 years now and LDN is the only med I've taken in years, other than antiobiotics and Advair 100/50

I had an MRI in an open machine in 1/03, 3 months before I started, and had an MRI in a closed Tesla 1.5 last August. They were identical except for finding a small 7mm lesion that didn't show on the open scans.