Here’s what’s happening at The Genesis Foundation For Children.
While most parents spend the first few days after delivery basking in the joy of bonding with their newborn, Tina and Chris Stuto’s world changed forever when, just two days […]
In 1996, when D.J. DiSilva was 3 and a half years old, his speech abruptly arrested and his behavior began to change. What his mom, Annie, didn’t know at the […]
“Wait and see.” Three words parents are often told by their child’s doctor when they have not reached a specific developmental milestone yet. According to Kalli Frankel, these words can offer both hope and worry.
Christine became a full-time caretaker of three young children at 68 years old. On January 6, 2018, Christine was granted custody of her great grandson, Noah, and his two siblings […]
The Genesis Foundation for Children is proud to announce that our Foundation President, Matthew Hoffman, is being featured on iHeartMedia Boston’s “CEOs You Should Know“. This radio and podcast segment […]
Wonderful things can be accomplished when non-profits support one another. Lovelane, located in Lincoln, MA, is a pediatric, therapeutic horseback riding program for children with special needs. In a typical […]
The Genesis Foundation for Children has announced a gift of $1,160,000 to Mass General for Children (MGfC) to expand wraparound care for patients with rare genetic conditions and their families. […]
It was the morning after Thanksgiving. Julie and Rick Cincotta woke up to a dolphin-like sound on their baby monitor. They immediately ran into their 3-month-old son Joey’s room to […]
February 28th – The Rarest Day of The Year Is Rare Disease Day February 28th is Rare Disease Day. “In the United States, a rare disease is defined as a […]
Neve is not your average ten-year-old fourth grader. Although you wouldn’t know it from looking at her, Neve has a rare genetic disorder called Trisomy X. One in 1,000 females […]
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