by Fetal Health Foundation | May 30, 2019 | Blogs, front-page, Myelomeningocele/Spina Bifida, News, Story
Most mothers would probably tell their child to sit down and stop standing on the chair in the middle of their family photography session. But when you’re told your son will never walk and he mischievously climbs onto a chair with no help and stands there, posing for the camera … well, you let him do it.
by Fetal Health Foundation | May 13, 2019 | front-page, Myelomeningocele/Spina Bifida, News, Story
This time last year, I was taking a pregnancy test. Today, I’m the mother of a healthy four month-old little boy who loves to smile and kick his legs like crazy.
by Fetal Health Foundation | May 13, 2019 | front-page, Myelomeningocele/Spina Bifida, News, Story
Johnna Kerres tells her story of the surgery she and her son underwent before he was born. The fetoscopic surgery contributed to medical research.
by Fetal Health Foundation | May 6, 2019 | front-page, News, Story
After a dangerous experience, mom Paula Yost Schupp encourages all pregnant women to be familiar with the signs of preeclampsia, even if they, like her, seem to have no initial risk factors. She tells her story of how she was diagnosed, and what happened as a result.
by Fetal Health Foundation | Apr 29, 2019 | front-page, Hydrocephalus/ Ventriculomegaly, Story, Ventriculomegaly
Logan’s story is so much bigger than his diagnosis. To fully understand you have to know I had a stillborn baby named Andrew 12 years before I had Logan. Andrew had the same diagnosis as Logan. I can never forget the day I knew something was wrong with Logan. We went...
by Fetal Health Foundation | Jan 23, 2019 | Cystic Hygroma, Fetal Hydrops, front-page, Story
Gina Harris is the CEO of Now I Lay Me Down To Sleep. In this piece she shares how important nurses have been in her life. “When I went into labor with my first baby on October 24, 2007, I did not know what to expect. I knew that our baby David would either be stillborn or he would die shortly after birth. He had Potter’s Syndrome, which means his kidneys never developed, thus preventing his lungs from developing…”