Sometimes the scariest things in life are the unknown. For Lea Whitehurst-Gibson and her husband, Monty, this became their reality when they adopted Samaj four years ago.

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Sometimes the scariest things in life are the unknown. For Lea Whitehurst-Gibson and her husband, Monty, this became their reality when they adopted Samaj four years ago.
Pediatric Therapy helps Ezra explore his community on a new prosthesis, spreading smiles and awareness At her 20-week ultrasound, Jessie received unexpected news: her son, Ezra, had proximal femoral focal deficiency (PFFD). PFFD is a rare birth defect where the upper part of the femur is missing or not fully formed. While Ezra’s knee, calf, ankle, and foot...
The following article was first published by the Robins Foundation. To view the original version, click here. Partner Spotlights are a platform for Robins Foundation grantees to highlight their important work and for Robins Foundation to recognize the incredible efforts and successes of our partners. This month, our Administrative and Operations...
Jack’s diagnosis is rare. So rare, that only ten cases of Warsaw Breakage Syndrome have been reported worldwide!
Luckily, Jack’s SOAR365 physical therapist is pretty rare, too. Sam Cipolla specializes in helping medically complex kids. “Jack is actually the one who made me realize that’s what I enjoyed,” says Sam.
Dr. Joe and April Niamtu donate generously to SOAR365, where their sons received pediatric therapy. When parents first learn their child has a disability, it can be a disorienting experience. “You don’t know what to do. You’re lost,” says Dr. Joe Niamtu. He and his wife, April, are parents to two sons with cerebral palsy: Joey and Evan. When...
SOAR365’s Pediatric Therapy program worked with the Haas family’s daughter, Betsy.
Now, nearly two decades later, the Betsy Haas Fund for Children is gifting Summer Camp scholarships to two young women.
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