SSM Health Cardinal Glennon Blog

Hope for Patients with Rare Genetic Liver Disease Hope for Patients with Rare Genetic Liver Disease

Jen Childress clearly remembers the day she first heard about a disease called Alpha-1 Antitrypsin (AAT) Deficiency. Learn more about her story and the advancement of treatment for this genetic disease.

Dec 27, 2023
Conner’s story: Exceeding expectations for seven years and counting Conner’s story: Exceeding expectations for seven years and counting

Read about Conner's journey with Missouri's top ranked NICU.

Oct 13, 2023
Managing cystic fibrosis is a team effort Managing cystic fibrosis is a team effort

At two weeks old, baby Robyn was diagnosed with Cystic Fibrosis.

Apr 19, 2023
Catching Up With Liam and Kaylin Catching Up With Liam and Kaylin

Their love of life continues thanks to the generous gift of organ donation.

Jun 07, 2022
My baby, his name’s Walker and he’s a warrior, he’s going to be a fighter. My baby, his name’s Walker and he’s a warrior, he’s going to be a fighter.

Gretchen shares the story of her pregnancy and new baby Walker, who was born with Down Syndrome.

Mar 18, 2022
As a young child, Abbi knew she would need a life-saving kidney transplant. As a young child, Abbi knew she would need a life-saving kidney transplant.

Abbi Penning’s family brought her to SSM Health Cardinal Glennon Children’s Hospital when she was two-and-a-half years old. Abbi was born with VATER syndrome.

Aug 03, 2021