Parenting

Baby Girl with SCID saved by Cord Blood Transplant

Not so long ago cord blood was considered a medical waste. But now almost every day cord blood transplants are helping give many like baby Valentina DeLeon a second chance at life & whose rare disorder could have turned fatal if not for the transplant.

Valentina DeLeon

Living in Rio Grande Valley, Valentina was 10 months old when her parents noticed that there was a problem with their baby daughter. Valentina weighed only 13 pounds.

“She was super skinny,” says Valentina’s mother, Karina Chapa. “She was sick all the time. She was vomiting. She was throwing up all the time. She wasn’t eating.”

The couple found out that their baby had a rare disorder called severe combined immunodeficiency (SCID). The condition became widely known in the 1970s when the world learned of David Vetter, a boy with SCID who lived for 12 years in a plastic, germ-free bubble.

Valentina DeLeon with her dad

Doctors sent Valentina to Methodist Children’s Hospital in San Antonio. Here, Dr. Ka Wah Chan ordered high-dose chemotherapy and cord blood transplant.

It was a lucky match when cord blood donated by a stranger turned out to be perfect for Valentina. The cord blood cells have the unique ability to create new cells in whichever part of the body there is the need. In Valentina’s case they helped create a new and stronger immune system.

“The cord blood is thrown away anyway,” Dr. Chan explained. “Nobody saves cord blood. But it can be used. And it can particularly be used in this type of situation when you can do a transplant and save a life.”

Valentina DeLeon with her parents

Five months after the transplant, Valentina weighs a healthy 21 pounds and doctors are optimistic about her future. Her parents consider her a miracle child and are immensely grateful to the cord blood donor who remains a stranger but saved their child’s life.

“It’s changed her life and it was a miracle,” Chapa said. “She’s alive and she’s healthy and I’m just thankful. Very thankful.”

From fighting a disorder that turns fatal in most cases to being a survivor, Karina adds that every day her daughter is alive is a celebration.

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About the author

Atula

Atula is a writer, traveler, and a nature-lover. She is also mom to a boy who seems to have inherited all her creative genes. When Atula is not busy making up stories with her son, she writes for numerous magazines, websites, and blogs. She is also working on her site on endangered species called indiasendangered.com.

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