I am happily married (10/30/05) to a wonderful full-blooded Italian. He gave me a Handsome Son who means more than the world to me. My son Robert Jr. was born on July 13,2006. Robbie was born with a Cleft Lip/Uvula and a Hypospadius; he has undergone 2 surgeries so far and both of them were a success. I started a Non-Profit Foundation called Little Robbie's Smile and as soon as we get enough funds we are going to start helping other families in need of getting the best care possible for their child with a Craniofacial Deformity. Although, Cleft's are "fixable" there are numerous surgeries to undergo and lots of money to shell out. Our son's one surgery alone was more than $70,000 and that does not cover the other surgery he had nor the surgeries he may need as he gets older. Thank heaven we had good Health Insurance, but think about the children who don't have the means to give THEIR CHILD the best care possible when our insurance company Cigna gave us such a hassle to cover our sons and who denied us 3x before we appealed for the final time. As a mother with a child whom was born with this deformity, I truly understand now more than I have ever before, that is more than why I want to be able to help those children who are not so lucky. Once our webpage is up and running I will post the website address and you can read more on Cleft Lips/Palates and the way it has become and epidemic in todays society.If you would like to know more, please do not hesitate to send me a message.MY HANDSOME LITTLE ANGEL ROBBIE JR.
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