Project ELI is a documentary containing stories of families that have children with spina bifida designed for new parents who just received their baby's diagnosis. Instead of being a medical look at spina bifida, it gives people the opportunity to "meet" families touched by this birth defect. You can request copies of the videos by e-mailing jodie@teameli.com. I am sending my copy to a local pregnancy center my friend runs (they just did an ultrasound on a mom and believe the baby may have spina bifida) and plan to order more to the specialist's office I had for our pregnancy. Spread the word... every life is worthy, and every life inspires!
I have just been catching up on your blog. Glad to hear that Madi is doing so well. I LOVED to see her move around in the bumbo chair. Her squeals were so cute.
I have just been catching up on your blog. Glad to hear that Madi is doing so well. I LOVED to see her move around in the bumbo chair. Her squeals were so cute.
ReplyDelete