Originally Posted By: Orch
I am not taking LDN. I asked my AS doctor about it, he knew nothing about it. I have not asked my MS doctor about it. I will try to remember next time I talk with her.

Butting in here to offer a suggestion. My doc didn't know about LDN, but printed out the info about what diseases it works for from this webpage , and I gave her the website to read. Tomorrow I'm taking her some more info from this site, because there are links to videos from the professional conference in... (Molly? Where was that again? ) Then it took two more visits before I was able to talk her into trying it, and my mobility is SO much better it's amazing. My cousin has had MS for 27 years, and she just started LDN in late September. She's having a good time with the improved energy. Good luck with your doc!

ANA+ RF+ Rh- HLAB27+
Dx JRA 1967, GAD 1997, AS 2009, HMs 2010, CPS 2013
pulmonary edema w/ NSAIDS 2009

Movin' it so I don't lose it!