Spina Bifida Stories


You are not alone in carrying your child with Spina Bifida to term. Here is what Angeline’s dad has to say to parents who have been given the adverse prenatal diagnosis of Spina Bifida:

“From the first day when we saw our daughter’s heart beating on the ultrasound monitor, Angeline became a real, living member of our family. Since then, we were committed to do anything humanly possible to improve her chances of having a better life. Emily and I are delighted with our little angel and we thank God for having given us the opportunity of partaking in one of His miracles. And we thank Him every day for having given us Angeline Marie.”

If you have a Spina Bifida story to share, please submit it to us by contacting mary@prenatalpartnersforlife.org.


The support, information and encouragement provided by the PPFL parents is not meant to take the place of medical advice by a medical professional. Any specific questions about care should be directed to a health care professional familiar with the situation.


Phone: 763-772-3868

Fax: 866-870-9175

Prenatal Partners for Life
PO Box 2225
Maple Grove, MN 55311

Email: mary@prenatalpartnersforlife.org