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What is HDFN?

What is HDFN?

by Erika K Wolf | Aug 6, 2024 | Alloimmune Thrombocytopenia, Blogs, front-page, HDFN, Hemolytic Disease, News, Rh Disease, Story, Uncategorized

2-minute read

HDFN is a rare fetal syndrome that affects later pregnancies. Johnson & Johnson is pioneering research to help women at severe risk. Their clinical trial is currently enrolling women who are at risk for severe HDFN who have a history of severe HDFN in a prior pregnancy.

Fetal Surgery: Seven Questions Dr. Timothy Crombleholme Answered for Us

Fetal Surgery: Seven Questions Dr. Timothy Crombleholme Answered for Us

by Fetal Health Foundation | Jul 30, 2024 | Blogs, front-page, News, Story

4-minute read

Renowned expert Dr. Crombleholme answers common questions about fetal interventions and treating babies before they’re born.

Logan’s Recovery  from Gastroschisis

Logan’s Recovery from Gastroschisis

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.

Agenesis of the Corpus Callosum and A Mom’s Letter of Thanks from Croatia

Agenesis of the Corpus Callosum and A Mom’s Letter of Thanks from Croatia

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.

Triplets and TTTS: The Craven Family Story

Triplets and TTTS: The Craven Family Story

by Fetal Health Foundation | May 24, 2024 | front-page, News, Twin-to-Twin Transfusion Syndrome

TTTS can affect Triplet pregnancies. Read about the Craven family and what their experience was like with a triplet ttts diagnosis.

Sacrococcygeal Teratoma: Complex Procedure Saves Baby with Rare Fetal Tumor

Sacrococcygeal Teratoma: Complex Procedure Saves Baby with Rare Fetal Tumor

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...
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What It Was Like For Our Family

Stories of Fetal Diagnosis and Treatment

Fetomaternal Alloimmunization: Alexandra’s Story

Fetoscopic MMC (Spina Bifida) Repair: One Family’s Journey

Spina Bifida Stories

TTTS Stories

Maternal Fetal Medicine and Fetal Syndromes: The Basics for Expectant Parents

Rose’s Prenatal Spina Bifida Story

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Expert Voices

Insight from Professionals

Gastroschisis and the search for better, earlier interventions with Dr. Geoanna Bautista

Q & A with a Trailblazer: Dr. Scott Adzick at CHOP

Dr. Chmait Performs Minimally-Invasive Fetoscopic Surgery for Spina Bifida

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What We Do: Our Annual Impact Report

Renny and Benny’s Story

Our Founders Story: The Somers Family

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Littleton, CO 80127

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