by Erika K Wolf | Oct 17, 2024 | Blogs, Cardiac Disease, Condition, Congenital Heart Disease/Defects, front-page, Hypoplastic Left Heart Syndrome, News, Story
3-minute read
Zane and Zeke are happy and thriving today after experiencing impossibly long odds of developing the same congenital heart defect. The exceptional care teams at Children’s Hospital Colorado provided cutting edge expertise and unwavering support for the entire family throughout both boys’ fight to survive.
by Erika K Wolf | Sep 3, 2024 | Blogs, Condition, Fetal Hydrops, front-page, News, Story, Uncategorized
3-minute read
University of California at San Francisco Hydrops Center of Excellence leads the way in Hydrops research. Funding from Brianna Marie and Fetal Health Foundations helps experts continue to deliver the latest in-utero treatments.
by Fetal Health Foundation | Jul 18, 2024 | Blogs, Condition, front-page, Gastroschisis, News, Story
~ 5 Min Read ~ “I’m always amazed when I see these babies at birth, and we put the bowel in a silo how we’re able to get that bowel back into the tummy in such a short period of time,” said Paul Wales, MD, surgical director for the Intestinal Rehabilitation Center at Cincinnati Children’s Hospital.
by Fetal Health Foundation | Jul 17, 2024 | Agenesis of the Corpus Callosum, Condition, front-page, News, Story
~ 3 min read ~
Dear Lonnie,
I wanted to thank you for being with me… those were very difficult moments. My heart is as big as a house. I wish you much success & health in the new year. I am sending a picture of my perfect son.
by Fetal Health Foundation | May 17, 2024 | Blogs, Condition, front-page, News, Sacrococcygeal Teratoma, Story
~ 6 minute read ~ This sacrococcygeal teratoma article appeared in the spring 2024 edition of Connexions, a magazine for the Fetal Health Community Rural Colorado couple Lyndsy and her husband, Aaron, found out they were expecting their third child, Ella, in November...
by Fetal Health Foundation | May 16, 2024 | Condition, front-page, Myelomeningocele/Spina Bifida, News, Spina Bifida, Story
When Katarina’s unborn baby was diagnosed with myelomeningocele (MMC), “It was kind of a shock, but my doctor said the best bet was fetal surgery. He referred me to Colorado right away, and he said we needed to do it as soon as possible,” she says. “That just kind of threw me for a whirlwind, and I have other kids to take care of too. It was a lot to process.”