Multiple Sclerosis
"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&#039;t have and have never had &quot;flare ups&quot; but at the rate I was going downhill before Copaxone, this is great.  I don&#039;t like the shots, but I know they are worth it."