Soda Springs family asks community for help with child's cerebral palsy treatment - East Idaho News
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Soda Springs family asks community for help with child’s cerebral palsy treatment

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SODA SPRINGS — What began as a routine prenatal appointment turned into a life-changing emergency for a Soda Springs family — and now, two years later, they’ve launched a GoFundMe to help pay for a potential treatment for their son’s cerebral palsy.

“You never think something like this will happen to you,” mother Chelsey Davids said. “And then it does. I just wish I could take away the challenges that he faces every day. And then I wish that I could just make things easy for him.”

This all started when Chelsey went to see her doctor for a routine appointment at 37 weeks’ gestation. She expressed concern that her unborn son, Clair, wasn’t moving. Medical staff found that Clair was only showing a heartbeat.

They performed an emergency C-section, and Clair was immediately rushed to the neonatal intensive care unit. Chelsey only got a peek of him before he was gone. Weighing five pounds, he stayed in the NICU for around 13 days.

While he was there, a neonatal neurologist informed Chelsey and her husband, Cache, that Clair had suffered brain damage. They warned it could be as serious as cerebral palsy or as minor as a learning delay.

More than six months later, he was officially diagnosed with Spastic Quadriplegic Cerebral Palsy, meaning the ailment affected his whole body.

VIEW THE GOFUNDME HERE

From left, Cache Davids, Clyde Davids, Clair Davids and Chelsey Davids pose for a photo. | Courtesy photo
From left, Cache Davids, Clyde Davids, Clair Davids and Chelsey Davids pose for a photo. | Courtesy photo

As Chelsey began researching treatments for cerebral palsy, she came across the Stem Cell Institute of Panama. She said they conduct additional testing of stem cells and identify six stem cells that help regenerate brain tissue the most. Of note, the treatment is not currently approved by the FDA.

“Kids with cerebral palsy, they have damaged myelin, damaged brain tissue, damaged pathways,” Chelsey said. “… They’ve actually found with stem cells that they’ve been able to reestablish some of those pathways and actually help somewhat heal the brain tissue and help the myelination process kick into overdrive.”

Chelsey said the institute has already approved Clair for treatment, and they’re set to tentatively go to Panama in early February. The only issue is that Medicaid does not cover the treatment. Therefore, every $15,000 treatment must be paid out of pocket.

Chelsey described her son as goofy. She said he’s recently finished intensive physical therapy sessions, and as they were driving back and forth from Soda Springs to Idaho Falls, he’d do little sit-ups and giggle like he’s saying, “Did you see that, mom?”

She said Clair also has his own language with his father. They click their tongues at each other.

“He thinks it’s the funniest thing ever, and I think that he knows that other people enjoy listening to him do that too,” Chelsey said. “That was a huge milestone for him to figure out his tongue placement and how to make that noise.”

Chelsey said one day she hopes to be able to sit down with Clair and have a conversation as simple as how his day is going.

“We’ve overcome it as well as we have because of our medical staff, because of our family, and because of our friends,” Chelsey said.

Our attorneys tell us we need to put this disclaimer in stories involving fundraisers: EastIdahoNews.com does not assure that the money deposited to the account will be applied for the benefit of the persons named as beneficiaries.

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