Skip to main content
Live Action LogoLive Action
10409051_821261014613707_6594081574724687776_n

Parents call baby born without a nose ‘perfect’

IssuesIssues·By Becky Yeh

Parents call baby born without a nose ‘perfect’

In the late afternoon of March 4, 2015, Eli Thompson was born a healthy, happy boy — but to his parents’ surprise, he was born without a nose.

Weighing at 6 pounds, 8 ounces, doctors told parents, Brandi McGlathery and Troy Thompson, that their newborn son was diagnosed with complete congenital arhinia, a life-threatening condition that results in the complete absence of the nose at birth.

11068273_870426066351008_2544388789832924830_n

“I pulled back and said, ‘Something’s wrong!’McGlathery told reporters. “And the doctor said, ‘No, he’s perfectly fine.’ Then I shouted, ‘He doesn’t have a nose!’ I was the first person to see it. Even when they took him away, my family still didn’t know something was wrong, due to being caught up in the excitement of his arrival. It wasn’t until they opened the blinds of the nursery that everyone else saw.”

There are roughly 30 reported cases of the condition, globally.

Shortly after birth, Eli naturally started to breathe out of his mouth. He spent his first few days outside of the womb in the Women’s Hospital’s neonatal intensive care unit, and required a tracheotomy and a feeding bag inserted into his stomach, but he has now transitioned to life at home.

13375_825794030827072_8524201772309570317_n
11057319_828665740539901_5422136031708922021_n

The condition affects Eli’s pituitary glands, McGlathery said, and he will be unable to undergo facial surgery to construct nasal passageways until past puberty. However, Eli’s parents explain that the decision for an artificial nose will be his to make —his parents love him just the way he is.

“We think he’s perfect the way he is,” McGlathery said. “Until the day he wants to have a nose, we don’t want to touch him. We have to take it day by day.”

“We’re going to do our best to make sure he’s happy. The rest of him is so cute, sometimes you don’t realize he doesn’t have a nose,” she said.

Live Action News is pro-life news and commentary from a pro-life perspective.

Contact editor@liveaction.org for questions, corrections, or if you are seeking permission to reprint any Live Action News content.

Guest Articles: To submit a guest article to Live Action News, email editor@liveaction.org with an attached Word document of 800-1000 words. Please also attach any photos relevant to your submission if applicable. If your submission is accepted for publication, you will be notified within three weeks. Guest articles are not compensated (see our Open License Agreement). Thank you for your interest in Live Action News!

Dear Reader,

Have you ever wanted to share the miracle of human development with little ones? Live Action is proud to present the "Baby Olivia" board book, which presents the content of Live Action's "Baby Olivia" fetal development video in a fun, new format. It's perfect for helping little minds understand the complex and beautiful process of human development in the womb.

Receive our brand new Baby Olivia board book when you give a one-time gift of $30 or more (or begin a new monthly gift of $15 or more) to fuel Live Action’s life-saving content.

Read Next

BREAKINGMifepristone tablets in box. RU-486 Medical abortion pills. Used in combination with misoprostol 3D rendering.
Abortion Pill

Missouri AG files lawsuit against FDA to restore abortion pill restrictions

Bridget Sielicki

·

Spotlight Articles