Lisa's recent life decision

About a year ago, I announced that I was diagnosed with MS.  Within six months of that diagnosis was wrong.  My new diagnosis is Stiff Person Syndrome (SPS).  It is a neurological muscular autoimmune disorder.  Basically my body has a mind of its own.  I can not move without the assistance of medication and a walker.  SPS is a rare condition.  Doctors gave me very little information about the disease.  Little is known but they do know there is no cure and it is a progressive disease.  My life span is questionable.  They say I will live a normal life span but their is a question mark in my mind.  The reason for the question is because of how much they (doctors) really know about the condition.  I have decided to try and redefine my life and talk to you about my new life adventure.