LDN

[Guest guest]

Good for you Marcie, for being your own patient advocate. I have been on LDN consistenely since Sept.1,2006. Was given tysabri Aug. 25,2006. Foolish me stopped LDN for tysabri. Next morning MS symptoms all were worse, with new sx's. Knew then I would never take anymore tysabri. Called neuro 1 week before next infusion that I would not be taking tysabri anymore. Neuro asked why and I told him what had happened. He told me it takes 3 treatments for the ty to work. My body said NO. Have been taking LDN, it has helped with alot of things. My slogren's and raynaud's that occured after a immunosuppressant drug, given to me by the neuro, LDN has stopped all there sx's. Not doing alot for the MS at this time, I am a patient person. It has helped in other areas, no reason to stop it. LDN I did have the terrible stiffness

that lasted over 2 months. I did feel I was getting worse MS- wise. Things that it has done for me, I am not giving up on LDN.. The reason I started LDN was for a terrible tightness in my buttocks. It did eleviate the tightness. Feel I did my body an injustice stopping the LDN. Even though I restarted the LDN a few days after the tysabri, it takes time for ty to leave ones system. This is just my experience with LDN. __________________________________________________