Un site LDN en francais : http://www.sep.over-blog.com
Un site LDN en francais : http://www.sep.over-blog.com
Enfin un site LDN en francais : http://www.sep.over-blog.com
Last edited by renaudjba on Mon Aug 11, 2014 4:14 am, edited 2 times in total.
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
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
Enfin un site LDN en francais : http://www.sep.over-blog.com
Fin de Màj 1 sept 2013
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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
Last edited by renaudjba on Sun Sep 01, 2013 6:14 am, edited 1 time in total.
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LarryLDN
- Family Member
- Posts: 50
- Joined: Thu Dec 11, 2003 3:00 pm
- Location: Staten Island, NY
- Contact:
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.
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.