This year we will be walking and raising awareness  for our daughter Neena Rey , born with a rare form of Hypoplastic Right Heart Syndrome if she is recovered from her heart surgery taking place in July. This little girl is a warrior amongst a lot of other children. CHD life is not easy but with new technology and research it can make a huge difference in these kiddos lives. 

We are asking our family and friends to join us at Willam Land Park on August 14th for the walk even if you cannot donate to the cause ❤

Raising funds for congenital heart defect (CHD) research is not only critically important to all babies born with, and children and adults living with CHDs, it is also personally meaningful to me.

By donating to help me reach my fundraising goal, you’re helping to fund the most promising research into CHDs - America’s most common birth defect.

Together we can make a life-saving difference! Thank you in advance for your support.