Here’s what’s happening at The Genesis Foundation For Children.
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 […]
By Laura Will Reprinted with permission from www.Knowrare.com I enjoy the goal-oriented practice of setting goals. However, I want to approach this year differently. Instead of using self-critical thoughts to […]