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Spina Bifida Stories
You are not alone in carring
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.
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