Tomorrow is national day of prayer for spinabifida. A mother whose child was recently diagnosed is debating about the possibility of aborting her baby because of his diagnosis. Now as a mom of spinabifida I know this is no reason to abort. My child is handsome, smart, silly, intelligent. He has an amazing spirit and brought much love into our lives. A fellow SB mom has set up this prayer day. To get more details of when to pray and things you can pray about click on this link. This pray day is for all faiths. Join there is strength in numbers.
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.