So you may have seen the post back in March about the Life as a Zebra Documentary that was released. You may have even watched it…related to it in some way…or even learned something.

For the month of February, I was followed by cameras as Max, the reporter, documented my life with EDS and POTS. 

Allie and I have danced together since the time she could walk.

We have continued to dance through gymnastics.  Through celebrations.  Weddings.  Funerals.  Sicknesses.  Concerts.  Recovery.

1.  Medical Stuff:

• No PT.  I was on my own all week.
• 2 Days of Home Rehab.
• I saw Larry in the office for lots of OMM.  My body got a much needed tune-up!
• This week was much more manageable in terms of what I needed to get done, and I realized a lot of that was due to a couple of factors:

Here it is zebra friends and family!

Dear friends, family, supporters, and fellow zebras,

Finally.

After months, and days, and hours, and hours…and more hours of planning, we are finally ready to launch ticket sales for our 2nd Annual, “An Evening with Chris Trapper to Benefit Invisible Illness Research.”