My name is Trevor. I am now almost 11 years old. This is me when I was almost 4. I was born with a cranio-facial disorder called hemifacial microsomia but Mommy & Daddy had no idea what that was or that I would be so special. I am just like every other normal boy on the inside - I like video games, basketball, playing with my friends, and I'm really smart too. But my outsides are different than most other kids, mostly just my face. I have been through five operations before I even turned 5 years old but Mommy & Daddy were there with me every step of the way. I don't really understand it all - to me I'm just a normal kid - but Mommy said that when I was in her belly this is how I grew, and my mouth wasn't big enough so the doctors had to make it bigger for me to eat properly and not choke, and for all my big boy teeth to come in. I had a lot of trouble walking & talking when I was a baby and I have had all kinds of special people in my life help me grow up to be who I am today. I only have one ear - the other one didn't finish growing when I was a baby and so Mommy & Daddy said that's just how God made me and that's exactly what I tell other people when they ask me. I call it my "little ear" and I don't ever want it to go away. I ask Mommy if I can keep it because I don't want the doctors to take it off. I don't really like going to the doctor very much although I do spend a lot of my time there. Since I have had so many things happen that I don't really understand, the doctors now say that I have Anxiety Disorder, but I just tell Mommy that I have lots of worries and thoughts in my brain that I can't stop and sometimes it feels like my head will explode! I know that there are other kids out there just like me because I see them every time I go to Children's Hospital of Philadelphia to see my team of doctors who make my outsides match my insides - beautiful. So Mommy, Daddy and I have decided that it's time to give back to all the people who have given to me - and that's what this website is for. You can see my journey here and the foundation that helps us and that we would like to help BACK so that they can continue to help other families who have kids just like me and more... I hope you will help us give some more hope to more families who need it!