'I just want to keep my son alive': Mom tries to find donor for 7-year-old

MIAMI – Everyday, Mayra Garcia wakes up with the same thoughts.

Is today going to be the day? Will she get the call telling her there's a match for her young son? Will he finally get the bone marrow transplant to save his life?

"It's getting harder every day," she said. "He's only a little kid. We need help."

Garcia, 31, who lives in Homestead, Fla., with her husband, Dany Morales, 34, said her life has been a waiting game since her 7-year-old son Julian was diagnosed with Dyskeratosis Congenita, a rare genetic disorder in which the marrow does not produce sufficient blood cells, when he was 3.

While he's on a medicine that has stabilized him, there are only a few more years it will work, doctors say. The only long-term treatment for him is a bone-marrow transplant, which replaces the damaged cells with healthy blood stem cells from the bone marrow.

Through the Minneapolis-based nonprofit, Be the Match, Garcia has held donor drives and had dozens of friends and family members tested, but none completely match Julian's DNA profile, necessary for the transplant. Complicating matters, according to Be the Match: Garcia is from Mexico and her husband is from Nicaragua, making it harder to match Julian's DNA profile, as there are fewer Hispanic donors.

"The more ethnically diverse your background is, the more difficult it is to find a match," said Amy Alegi, vice president of marketing and communications for Be The Match.

Brandyn Harvey, a former NFL player, said he is a true believer in being a donor. He was in college at Villanova University when he first learned about becoming a donor through an outreach campaign around 2005. In 2016, he got a call saying he was a perfect match to save someone's life.

"I believe in second chances in life," said Harvey, now a Los Angeles personal trainer. He later learned his donation saved the life of a 66-year-old man with leukemia.

Garcia said when Julian was born on Sept. 18, 2011, he was a happy baby. As time went on, though, she began to notice her baby looked yellow, was crying a lot and "wasn't acting right."

She took him to several pediatricians and was told to take him out in the sun. Then she noticed a lesion on his tongue. One day, a pediatrician said she thought Julian had cancer.

Garcia took him to Baptist Hospital. He was there for four months, being treated with steroids and hormones. But he didn't seem to be getting better.

Along the way, doctors told her it could be a blood disorder. She then started researching the best treatment centers for blood disorders and stumbled on Boston Children's Hospital. She took him there when he 3.

She finally got the diagnosis, Dyskeratosis Congenita, which is very rare.

The doctors told her it should be easy to get a bone marrow donor. She started carrying swab kits in her car, needed to collect a sample. She flew to California to ask family members she never met to get tested. She considered having another baby that possibly could be a match, but because she is a carrier of this disorder, she and husband have talked about in vitro fertilization.

All the while, she has struggled to keep Julian happy and as healthy as possible. He is now a first-grader in a small private school.

When he's not in school, his mother keeps him close. Due to his compromised immune system, he can't go to birthday parties, playgrounds, water parks — any of the typical childhood activities. "I keep him in a bubble," she said.

Julian, who likes play with his little sister Isabella, 4, says he can't wait to get his "match." She's not a match, nor are his parents.

"I'll get to go to water parks," he said. "When I feel better I can do anything."

Garcia, who set up a GoFundMe account to help with medical expenses, said seeing her child in pain is the hardest thing."I just want to keep my son alive," she said. "It's scary. Sometimes I feel it might not happen