BEAVERTON, Ore. (KOIN) — Just 21 months ago, Tommy and Linda Pham welcomed their son Raiden into this world. But when he was 3 months old they noticed something was wrong.

“He wasn’t hitting milestones. He started puking a lot. I thought it was me. I had so much milk, so the doctor said try the bottle and I did that but he was still puking 10 times a day,” Linda told KOIN 6 News.

That launched the Phams into a series of medical visits and tests but doctors couldn’t pinpoint what was going on until this past summer. That’s when the Phams had all 20,000 of Raiden’s genes tested.

This time the doctors found something.

Raiden has a UBA-5 gene mutation, a life-threatening progressive neurological disorder.

“There’s not a lot known about it. It’s ultra rare. It’s beyond rare,” she said. “Only 30 or 40 cases in the world.”

There’s no treatment. And no cure.

Linda and Tommy Pham formed the Raiden Science Foundation to raise money for gene replacement research for their son, December 2021 (KOIN)

After a month of being in a dark place, Tommy said he started using his contacts in the medical research field and eventually heard from the University of Massachusetts. Their researchers are interested in coming up with gene replacement therapy for UBA-5.

The Phams jumped on the opportunity and formed the Raiden Science Foundation to raise money for the research.

“We decided to launch on Thanksgiving,” he said. “Oh my God, the amount of support, just a small community. People are re-sharing, re-posting.”

They need $1 million to get going. As of Thursday, just weeks into the effort, they had raised more than $156,000.

GoFundMe: Race against time to defeat UBA5

Officials with U-Mass told KOIN 6 News the money raised would be likely used for 3 purposes:

Research to develop gene therapy vectors specific to UBA5
Hiring scientific research staff who would be dedicated to this project
Conducting initial, pre-clinical studies for efficacy and safety

The efforts are boosting their spirits, even with the uncertain future for Raiden.

Raiden Science Foundation

“As a mom it’s, like, there’s nothing you can do but just hope,” Linda said.

Over time, the Phams will need to raise $2 million to $3 million. With ultra rare cases, it’s common for families to get involved in fundraising since there is typically no government funding.