|Date||Sunday, May 05, 2013|
It’s that time of year for the Spina Bifida Association of Colorado’s Walk N Roll. This year is going to be the best year yet, but we need your help. We would love to have you join us on May 5 at Washington Park.
On June 10, 2008 our lives were changed when we were told our unborn child had Spina Bifida. I remember feeling like I was in a dream. I couldn’t have imagined anything worse. Today, our life is a dream. I am blessed by an amazing family, a great husband and two sweet children. Although Evan has some extra needs he is my inspiration. At the age of three he has endured 17 surgeries, countless nights in the hospital, doctors appointments, therapies and more. After all these things, Evan continues to amaze us each day and prove that you can overcome anything.
Along the way the Spina Bifida Association of Colorado has been by our side. We have made friends, had advice, encouragement, and assistance both financially and emotionally. Please help support a cause and an association very close to my heart.
Support Lisa Maskus here!