In 2005, our family grew with the addition of our daughter Sarah. Sarah was born with Cornelia de Lange Syndrome (CdLS). Throughout her years, we have had support from our family, friends, therapists, nurses, doctors, and the CdLS Foundation. In 2008, our family began giving back to the CdLS Foundation through generous giving at "Sarah's Bowl for CdLS". Fast forward 10 years and our local bowling alley has closed. We still want to support the CdLS Foundation, so they can continue their mission of Reaching Out, Providing Hope, and Giving Help. So this year, in lieu of an actual event, we are campaigning for donations on Crowdrise or by direct donations to the CdLS Foundation.
We have had the most wonderfully generous family, friends, and strangers donate, on behalf of Sarah to the CdLS Foundation. We hope to continue this tradition, while we try to figure out a type of fundraiser that may be more appropriate moving forward.
Thank you for your time and consideration,
Mike and Anne