When i was on meds, copaxone then rebiff, took them with understanding that they would prevent or reduce severity of relapses. As mri’s attested, ms was active at that time and i believed the injections were necessary to prevent a terrible worsening. Eventually course of ms seemed to change, two consecutive mri’s showed no active lesions, and i made decision to come off dmds, and began to concentrate on removing inflammation, taking vitamin supplements, diet change, exercise. Thats where im at today, no relapses, but dealing with a few ever present symptoms; heat intolerance, leg weakness, balance and memory issues, but overall feel grateful and pretty good

Ocrevus has been a game changer for me. I have been on it since January, no new lesions, plus after my last infusion on August 1st I'm walking without a cane & my gait is better. I also have been taking supplements, calcium, magnesium, vitamin D & MCT oil powder.

So glad so many were willing to respond.

Am taking Tysabri, Dalframidie,,Muti-vitamin etc. Was wearing a foot brace due to foot drop. This actually helped,to where I don't need o wear right now.