980-224-0398 [email protected]
Fetal Health Foundation
  • HOME
  • FETAL SYNDROMES
  • STORIES
  • ABOUT US
    • ABOUT US
    • SOMERS FAMILY STORY
    • OUR MISSION
    • OUR TEAM
    • FINANCIAL DOCUMENTS
    • MEDICAL BOARD OF DIRECTORS
  • MAKE A GIFT
Select Page
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.

Cord Blood Banking: What Expectant Parents Should Consider

Cord Blood Banking: What Expectant Parents Should Consider

by Fetal Health Foundation | Jul 13, 2024 | Blogs, News, Story

Is cord blood banking something you should do?
As you eagerly await the arrival of your little one, nothing is more important to you than ensuring the health and safety of your child. At this incredible time of your life, have you considered cord blood banking?

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...
« Older Entries
Next Entries »
Share Your Story

Fetal Syndrome Stories

  • Abdominal Wall Defect
  • Agenesis of the Corpus Callosum
  • Alloimmune Thrombocytopenia
  • Aortic Senosis
  • Bowel Obstruction
  • Cardiac Disease
  • Cleft Lip and Palate
  • Cloaca Exstrophy
  • Congenital Chylothorax
  • Congenital Cystic Adenomatoid Malformation
  • Congenital Diaphragmatic Hernia
  • Congenital Heart Disease/Defects
  • Conjoined Twins
  • Esophageal Atresia with Tracheosphageal Fistula
  • Fetal Cardiac Abnormalities
  • Fetal Chylothorax or Hydrothorax
  • Fetal Hydrops
  • Fetal Hypothyroidism/ Hyperthyroidism
  • Gastroschisis
  • Hemolytic Disease
  • Hydrocephalus/ Ventriculomegaly
  • Hypoplastic Left Heart Syndrome
  • Intrauterine Growth Restriction
  • Kidney, Bladder, and Genital Abnormalities
  • Lower Urinary Tract Obstruction
  • Meningocele
  • Myelomeningocele/Spina Bifida
  • Neurological Defects
  • Non-Immune Hydrops
  • Omphalocele
  • Pericardial Teratoma
  • Pleural Effusion (Hydrothorax)
  • Pleural Effusions
  • Pulmonary Agensis
  • Pulmonary Atresia with Intact Ventricle Septum
  • Pulmonary Sequestration
  • Rh Disease
  • Sacrococcygeal Teratoma
  • Selective Intrauterine Growth Restriction
  • Twin Reversed Arterial Perfusion Sequence
  • Twin-to-Twin Transfusion Syndrome
  • Ventriculomegaly
  • 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

    Make a Donation

    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

    Our Medical Board of Directors

     

    Who We Are

    A Parent-Founded Nonprofit

    What We Do: Our Annual Impact Report

    Renny and Benny’s Story

    Our Founders Story: The Somers Family

    Learn about our Flagship Fundraiser, The Great Candy Run

    Contact Our Staff

     

    980-224-0398
    9786 South Holland St.

    Littleton, CO 80127

    Privacy Policy