A few years ago my daughter Julie was diagnosed with an illness called Dysautonomia and Postural Orthostatic Tachycardia (POTS). Julie had numerous hospital visits requiring many tests and procedures. The costs were astronomical. Julie continued to be covered under my insurance through my employer who provided a great plan. Julie's insurance was to soon come to an end because of her age but her illness was getting worse and Julie's health deteriorated severely at the end of 2010. Julie was blacking out daily and unable to continue work or school. There were days when she only had the energy to crawl to the bathroom. Julie had a heart monitor installed as her doctors believed there was a possible underlying heart condition.
said, "Mom, they're pink!"  It had been a long time since blood had reached her extremities.  Holding her warm hand after surgery, warmed my heart.  As I stared at the heart monitor now pulsing with a regularity I hadn't seen all week, I swear I could see the changes in her face as the blood seemed to be bringing the needed oxygen to her every part of her body.  Julie's heart is now beating more regularly and helped daily by her pacemaker.  She is not completely healed.  The coming months will show how many of the symptoms of Dysautonomia remain.  Since the pacemaker though she has not blacked out which previously was an almost daily occurrence rendering her unable to do almost anything most days.P.S. I want to add: I find so many people that I talk to aren't aware of their options and don't know where to go. Here's a terrific resource to help you get started if you're in this position: http://www.gettingcovered.org/toolkit/#
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