Author Archives: sMiles 4 Sammy

In the News at the Ripken Foundation!

In the News at the Ripken Foundation!

Check out the In the News section on the Cal Ripken, Sr. Foundation’s Webpage, http://www.ripkenfoundation.org/news.php and scroll to the August 3rd entry!  The Ripken Foundation  asked us to send in an article and pictures of the silent auction and 5K, but we never imagined that they would be posted front and center on their main webpage!

To give you an update on the progress of the field:  To date, $65,000 has been raised for the field.  The Ripken Foundation and the East Wilco Challenger League of Hutto are working hard on grant applications, sponsorships, etc. to raise the remaining $285,000 to make this All Ability field a reality in Central Texas.  If you have some time, go to http://www.ripkenfoundation.org/ydpark.php and check out the many cities that the Ripken Foundation is impacting.  It’s amazing all that they have done to help children with special needs and disadvantaged youth through these fields and the game of baseball!  It takes time (sometimes years!) to complete projects like this, but both the Ripken Foundation and the EWCL are committed to seeing this project completed for the youth in our area.

Our group was blessed to be able to raise money in memory of Samantha for this awesome cause.  We are grateful that there are groups like the Ripken Foundation and East Wilco Challenger Sports that we can support!

Welcome to sMiles 4 Sammy

Welcome to sMiles 4 Sammy

 

The mission of sMiles 4 Sammy is to encourage people to see that life is not about the length of time we live, it’s about the way we live in the in the length of time we are given. Every day is a gift and a healthy body is a gift. What can you do in 10 months?

The sMiles for Sammy Team was created in memory of Samantha Scott.  Diagnosed with Trisomy 18 several months before birth, Sammy was expected to be stillborn as this condition is considered incompatible with life. She defied the odds and was given ten gift months with her family. During these ten months, her family made a decision to see each day as a gift and to focus on living life instead of being defined by a diagnosis.