Copaxone
"I was diagnosed July 2012.  Finally!  I could no longer walk, my legs had gotten so weak.  Was in a wheelchair already.  PPMS is not fun.  I have noticed that my legs are stronger, but still not able to walk.  And my MS has not gotten any worse.  Don't have and have never had "flare ups" but at the rate I was going downhill before Copaxone, this is great.  I don't like the shots, but I know they are worth it."