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The Best Possible Chance at a Fantastic Life

The Best Possible Chance at a Fantastic Life

by Fetal Health Foundation | Aug 28, 2019 | front-page, Myelomeningocele/Spina Bifida, News, Story

I saw my physician’s name come across my phone screen, and my heart sank. He explained that the ultrasound showed an abnormality, and he predicted a spina bifida diagnosis. I had no idea what that meant, and the rest of the words coming out of his mouth became a blur.

Spina Bifida Research at UC Davis Provides Hope

Spina Bifida Research at UC Davis Provides Hope

by Fetal Health Foundation | Aug 6, 2019 | front-page, Myelomeningocele/Spina Bifida, News, Spina Bifida

Spina bifida, which literally means “cleft or split spine,” is the most common permanently disabling birth defect in the United States. According to the Centers for Disease Control and Prevention, about 1,645 babies are born in the U.S. with spina bifida each year.

Curing Spina Bifida

Curing Spina Bifida

by Fetal Health Foundation | Jun 12, 2019 | Blogs, front-page, Myelomeningocele/Spina Bifida, News, Resource News, Sponsor

Growing up in the 1960’s, Dr. Diana Farmer’s mother taught Sunday school for disabled children where she first met children who had spina bifida.
“It was a really crummy disease,” Farmer said. Dr. Farmer is now leading innovative research, which holds promise of saving lives and lifetimes.

VIDEO: Fetal Surgery to Treat Paralysis Associated with Spina Bifida

VIDEO: Fetal Surgery to Treat Paralysis Associated with Spina Bifida

by Fetal Health Foundation | Jun 10, 2019 | front-page, Myelomeningocele/Spina Bifida, News, Resource News, Sponsor

In the video she discusses the improvements that resulted from the initial fetal surgeries, including a reduction in the need for shunts.  She now believes that with the latest breakthroughs involving fetal surgery and stem cells that the paralysis associated with spina bifida will be cured in her lifetime.

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