This is the joy of our lives, Cayson. He was born on November 13th, 2002 after a hard labor. We took him home after 2 days in the hospital.

They didn't know anything was wrong with him until he was about 2 months old, when they heard a heart murmur. After that, it all went very fast.

We got him diagnosed with supravalvular stenosis, periphial pulminary stenosis, renal artery stenosis and carteroid artery stenosis. He was then diagnosed with Williams Syndrome. He has high blood pressure, reflux, and he had an inguenal hernia removed. Besides that he hasn't had to have any surgeries yet.

We feel very blessed about that, and also to have him in our lives. The first few months after the diagnosis were hard. But he really has been such a joy to have in our family. He just lights up a room. I can't wait until he starts to talk, and he can almost walk.

We love him very much, and wouldn't trade him for the world.

We live in Las Vegas, and would love to hear from other families with Williams Syndrome children. E-mail us at nttamcclure@msn.com