Fetal Surgery for Morgan & Abigail

Our family was full of hope, excitement and anticipation for our 20 week ultrasound.  We brought our 9 year old son with us and  I don't know who was more excited our son or us!  After telling us it was a GIRL, the tech told us to wait for the doctor and then we could leave.  After what felt like a lifetime our Doctor came in and his face said it all.  Everything we had planned for our little girl changed once he said " I'm sorry but I don't have good news" We learned that Abigail has Open Neural Tube Defect (Spina Bifida) which was also pulling on her brain stem.  They sent us right over to Children's Hospital where we had a full day of tests and meetings. At our meeting we were able to learn more about Abigail's condition and what were our options in helping her.  Abigail's back is opened from L3 to L4, which controls her knee's ankles and bladder function, and her left Asymmetric Ventricle in her brain was dilated.  We qualified for either Fetal Surgery or post Fetal Surgery.  We have chosen to go with Fetal Surgery. The benefits out weighs the risks for us, we were ready to do what was needed to help her.  With the surgery I will no longer be able work due to being on bed rest until she is born. With this being a high risk surgery, she could be born premature, the doctors are hoping to keep her in until I'm 34 weeks though they would love if I made it to 37 weeks. Our insurance will only pay a little which is better than nothing, though with me not working it makes paying these medical bill near impossible. We are asking for any financial help in giving our new daughter the best life possible.