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Kidney Defects / Potter's Syndrome
Stories
You are not alone in carrying
your child with Potter's Syndrome or other kidney defects
to term. This is what Michael’s mom has to say
to parents who have been given the adverse prenatal
diagnosis of Potter’s Syndrome or other kidney
defects:
“Even though Michael didn't
live very long, we are at peace in our hearts with the
decision we made about allowing Michael to live according
to God's will and not by our own accord. Our lives have
truly been blessed through the years and our faith strengthened,
as a result of this little saint who was given to us
for such a short time. We came to realize that none
of our children are really ours. They are given to us
from above to love and care for and eventually they
will all return to the Father. We are so thankful that
we chose life for Michael.”
If you have a Kindey Defects
or Potter's Syndrome 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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