Life\’s For the Living
When the summer started I had this grandiose idea that I would blog all summer. Like real, meaty posts rather than just the quick “Five for Friday” check-ins that allow me to keep a quick record of life.
Just a "zebra" trying my best to live life to the fullest with EDS and POTS...and loving the ride.
When the summer started I had this grandiose idea that I would blog all summer. Like real, meaty posts rather than just the quick “Five for Friday” check-ins that allow me to keep a quick record of life.
For documentation sake, the following are Allie and my speeches from the Life as a Zebra Foundation’s second annual, “An Evening With Chris Trapper and opener, Joshua Davis Trio, to Benefit Invisible Illness Research” held at the Kellogg Hotel and Conference Center on April 13, 2013.
1. Medical Stuff:
Let’s face it. It’s hard to feel attractive in your own skin when you feel like your body is turning on you.
Topic: What questions do you have for other patients?
One of the most important things for me is sharing with fellow zebras. There is nothing like being able to talk to someone who is living a life similar to mine. I’m sure many of you will understand what I mean when I say what an amazing feeling it is to meet someone who just “knows” what you are going through, because they are living it too.