TOLD SHE MIGHT NEVER SEE HER FIRST BIRTHDAY, TEEN WITH RARE FACIAL TUMOR NOW DREAMS OF STUDYING NURSING AT STANFORD

A teenager once given little chance of surviving infancy is now preparing to graduate from school and pursue her dream of becoming a nurse.
Jacqueline Rodriguez, from California, was born with an extremely rare condition known as lymphatic malformations, which caused a large tumor-like growth to develop across her cheeks and tongue.

The condition has left Jacqueline unable to speak verbally and unable to eat normally, requiring her to communicate through an iPad and receive nutrition through a feeding tube.
Yet despite spending much of her life in and out of hospitals, the determined teenager has refused to let her condition define her future.

Today, Jacqueline hopes to study nursing at Stanford University, inspired by the healthcare workers who helped care for her throughout her childhood.
“I want to be a nurse because I grew up in a hospital helping my nurses take care of others,” she said. “The future is bright.”
Her remarkable journey began before she was even born.

During pregnancy, doctors warned her parents, Evelyn Belen and Paul Rodriguez, that their daughter might face severe challenges and may not survive beyond infancy.
“When I was pregnant, doctors told us Jacqueline might not live to see her first birthday,” her mother recalled. “Now she is achieving so much. I never imagined we would be here, and I am incredibly grateful.”

Throughout her life, Jacqueline has undergone numerous procedures aimed at reducing the growth. However, the mass repeatedly returned. While there is currently no cure, doctors have found treatments that appear to have slowed the growth and improved her comfort.
“With the medication she is taking now, the growth has stabilized and softened,” her mother explained. “She can make more facial expressions, and she is feeling much better than before.”

But the physical challenges have not been Jacqueline’s only obstacle.
She admits she has often faced stares and unkind comments from strangers because of her appearance.
“People point and stare,” she said. “Sometimes they say hurtful things. It makes me sad because they don’t know who I am. I’m a normal human being.”

Rather than allowing those experiences to hold her back, Jacqueline focused on the things she loves most.
She spends her free time playing tennis and guitar and says sports have helped build her confidence.
“Tennis reminds me that I am strong enough to do difficult things,” she said.

Her family says that same determination is what has carried Jacqueline through every challenge she has faced.
“I have no doubt she will succeed in whatever she chooses to do,” said her father, Paul. “She is the most amazing person I’ve ever known. She has faced so many obstacles and still wakes up every day with a smile.”
Her older sister, Anna Belle, agrees.

“Jacky inspires everyone around her,” she said. “If there’s something she wants to accomplish, she gives it everything she has. I’m incredibly proud of her.”
As graduation approaches, Jacqueline is focused not on the difficulties of her past, but on the opportunities ahead.

Supported by a close-knit family, loyal friends, and a determination that has carried her through years of medical challenges, she continues proving that a diagnosis does not define a person’s future.
“My parents always tried to make my life as normal as possible,” Jacqueline said.

And now, the teenager who was once not expected to reach her first birthday is looking ahead to college, a career helping others, and a future filled with possibility.