If you, your child or someone you know has been diagnosed with 16p11.2 deletion, it may feel overwhelming or unclear. That’s how it felt for my husband and I when our 3 year old son was diagnosed in 2014. We created this website and foundation to support you in your journey and provide for you everything we wish we had. There is a lot of information on this website. We have purposefully tried to make the website calm and the information easy to digest.