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Here’s what’s happening at The Genesis Foundation For Children.

Meet some of our inspiring patients.

Make A Gift, Change A Life

Updated on February 9, 2022

Today is Giving Tuesday, the global movement that raised $2.4 billion last year for nonprofit organizations to help transform our communities. After another unprecedented year living amidst a pandemic, we […]

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Bella and George

“She’s Fine, She’s Just Skinny.”

Updated on February 9, 2022

“She’s fine; she’s just skinny,” was what the pediatrician told Rachel Burton when her daughter, Bella, was two-and-a-half years old. Bella’s “failure to thrive” diagnosis meant that her height and […]

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Happy Thanksgiving & Get Ready for Giving Tuesday

Updated on February 9, 2022

Happy Thanksgiving from our family to yours! Last week, we discovered that $2.4 billion was donated in 2020 on Giving Tuesday from 75 different countries. To understand the sheer scale […]

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Did Someone Say, “Super Bowl”?

Updated on February 9, 2022

Did someone say that the Super Bowl is coming up? You thought that was in February, not in November. For nonprofit organizations, the equivalent of the Super Bowl is Giving Tuesday – […]

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Honor Murray Feingold’s Legacy

Updated on February 9, 2022

Some of you have shared your fond memories of Dr. Murray Feingold with us over the past four weeks as we have honored his memory by celebrating all that he […]

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Getting A Diagnosis Was Life-Changing

Updated on February 10, 2022

When Tina and her husband, Ernie, had their second daughter, Myla, they knew early on that something wasn’t right. Myla wasn’t hitting her developmental milestones. Unlike their older daughter, Myla […]

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Explosion in Medical Knowledge Doesn’t Make It Easier for Affected Families

Updated on February 10, 2022

Learn how the advances in medicine do not ease the burden on the family for children born with rare genetic disorders. Where medicine may not be able to help, The […]

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Patient Continues Dr. Murray Feingold’s Legacy

Updated on February 9, 2022

  Tom Hamel was born in 1973 with Treacher Collins syndrome, a rare genetic disorder characterized by abnormalities of the head and face. Tom’s parents brought him to Dr. Murray Feingold when […]

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Rachael Feingold Stein’s Tribute to her Father Dr. Murray Feingold

Updated on August 9, 2021

Since 1982, our mission to provide coordinated care for children born with rare diseases or genetic disorders has not wavered. In addition to funding The Feingold Center located at Boston […]

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