Kris was left paralyzed from the neck down after a car accident.
“I couldn’t drink, I couldn’t feed myself, I couldn’t text or pretty much do anything. I wasn’t really living my life, I was existing,” said Kris.
In April 2016, Kris participated in a clinical trial at USC funded by California’s stem cell institute. He received a single injection of 10 million oligodendrocyte progenitor stem cells (cells that insulate nerve cells).
Since the stem cell transplantation, Kris has regained significant use of his upper body. He can text, play with his dog, and lift weights over his head.
“After the stem cell surgery, I’m able to live my life again,” said Kris.
The stem cell treatment Kris received advanced to Phase 2 clinical trials, with results showing improved motor function in over 95% of patients.
Rosie thought she may never be able to see her twin daughters.
Rosie had slowly been losing her eyesight since childhood, but doctors couldn’t figure out why. While in her 30s and pregnant with twins, she was diagnosed with Retinitis Pigmentosa, a genetic eye disorder that can lead to complete blindness.
“It was absolutely devastating to know that I would be a mom and that I would eventually go blind,” said Rosie. Eventually, she did.
In 2016, Rosie participated in a clinical trial funded by California’s stem cell institute. She received an injection of retinal progenitor stem cells (the cells that give rise to the nerve cells in the eye). Seventeen months after the treatment, Rosie was able to see her twin daughters, make out her own handwriting, and look into her own mother’s eyes.
“People say hindsight is 20/20. But now when I think about it, I think, oh no, my future is 20/20,” said Rosie.
Every participant in this Phase 1/2 study experienced improved eyesight as a result of this treatment. The trial has advanced to Phase 2.
Evangelina was born with severe combined immunodeficiency (SCID), also known as “Bubble Baby disease,” a deadly genetic disease that causes babies to be born without functioning immune systems.
Her parents, Alysia and Christian, were among the first to put their faith in a groundbreaking clinical trial conducted at UCLA. Evie’s own blood stem cells were isolated, the missing gene was added, and the “corrected” cells were returned to Evie.
Evie is now cured of the disease. Alysia describes her daughter as “a healthy 5-year-old, vibrant, nonstop little girl with a functioning immune system."
Her father, Christian, was also astounded by the positive outcome: “It’s hard to believe until you actually see the results.”
Over 50 children have now been cured of Bubble Baby disease using this approach. The treatment has been fast-tracked to receive FDA approval.
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