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The Life-Changing Impact of Mental Health Care in the NICU

The Life-Changing Impact of Mental Health Care in the NICU

by Erika K Wolf | Mar 14, 2025 | Blogs, Condition, Esophageal Atresia with Tracheosphageal Fistula, front-page, News, Story

The mental health support provided in the NICU was essential for Collette & Alex as they navigated the emotional challenges of their daughter Austen’s critical care. The family-focused care at Stanford Children’s enabled them to manage stress, connect with other parents, and focus on both Austen’s healing.

Meet Rami: Checking off milestones after highly rare CCMS diagnosis

Meet Rami: Checking off milestones after highly rare CCMS diagnosis

by Erika K Wolf | Mar 6, 2025 | Blogs, Condition, front-page, News, Story, Uncategorized

Rami’s parents knew when he was still in utero that there was an issue with his jaw. Genetic testing after birth revealed an extremely rare diagnosis of CCMS, which affects the jaw, mouth, and ribs. Thanks to the compassionate, expert care at Cincinnati Children’s, Rami is almost 2 and keeping his parents on their toes!

What does the Fetal Health Foundation do?

What does the Fetal Health Foundation do?

by Erika K Wolf | Feb 14, 2025 | Blogs, front-page, News, Story, Uncategorized

At the Fetal Health Foundation, our mission is to connect patients with trusted treatment options and essential support resources. We collaborate with hospitals, fetal centers, and medical companies to amplify our impact. We strive to create a brighter, healthier future for mothers and babies!

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

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

by Erika K Wolf | Jan 9, 2025 | Blogs, Condition, Fetal medicine, Fetal surgery, front-page, News, Story, Uncategorized

The field of fetal diagnosis and treatment is continually evolving. Hear from Dr. Scott Adzick, one of the foremost trailblazers in the specialty, about groundbreaking advancements he helped pioneer. Learn why he believes it’s an obligation of the field to conduct research to offer hope and health.

Baby MJ Battles an Extremely Rare, Strange Heart Defect and Wins

Baby MJ Battles an Extremely Rare, Strange Heart Defect and Wins

by Erika K Wolf | Dec 21, 2024 | Blogs, Condition, Congenital Heart Disease/Defects, front-page, News, Story

The Egan family is grateful for the “enormous team” at Stanford Medicine Children’s Health who repaired baby MJ’s rare congenital heart defect and provided months of individualized care in the Cardiovascular Intensive Care Unit. Today, their baby is a thriving toddler with normal heart ventricle function.

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