Watch this video for my son. "He is no different then you my friend" I feel so blessed to have Tyson in my life. He is no different then anyone else. I would have loved to have viewed this video when I was pregnant. These babies deserve a shot at life. When I was at SB clinic this Friday. Dr. walker told us that in Utah 15-20 babies are born each year with Myelomeningocle Spina Bifida. Utah has the highest rate. He said mostly because not many abort. It makes me sad to think so many babies don't get a chance at life just because they have Spina Bifida. They are no different the you my friend. I have learned so much and want an feel learned so sooo blessed to have Tyson. Watch this for our Family!!!!
We are The Thomas Family! I am Jessica mom, wife and nurse. Jared is a railroad man. He works for Union Pacifc Railroad Jared and I have been married for 6 years. We have a 5 year old princess Chloe and a 2 year old stud Tyson. Tyson was born with Spina Bifida and Charii I Brain malformation. We had sugergy in utero on him and I on Feburuary 26, 2009. We were part of the MOMS study. To read more about Tyson read his blog by clicking on his name. Also for more information on the MOMS study visit http://www.spinabifidamoms.com/. Enjoy!
Chloe Anna Thomas
She's 5. She is 100% girl. Her favorite Color is pink. she is obsessed with Disney Princesses and claims she is one. She loves to get dressed up and already has a opinion on what she wants to wear. She also loves her baby brother. She keeps us busy and makes us laugh everyday.
Click on the image to visit Tyson's "website
Tyson Jared Thomas
"Our miracle baby". 2 Years old. He was Born at 4lb.s 3 oz with Myelomeningocele Spina Bifida and severe Charii I brain malformation. He is so chill! He has aready brought much joy into our lives. We love him so much! He is such a boy and loves making messes and the outdoors.