Young Professionals Summer Mixer
Posted on August 2, 2023The Genesis Foundation’s Young Professionals Committee is back for another summer event in the city. Join us on Wednesday, August 23rd for a great night at Fenway Park’s exclusive outdoor […]
Blog & News
Here’s what’s happening at The Genesis Foundation For Children.
News
We’re Making An Impact, So Can You.
Updated on February 9, 2022We’re making an impact, so can you. In 2021, The Feingold Center for Children saw 950 patients, that’s a 63% increase versus the year before. Of these patients, approximately 55% […]
Blogs
Defying The Odds
Updated on February 9, 2022Your Daughter Will Never Walk or Talk. Defying the odds, Amy never thought she’d be able to have children. Her pregnancy was high-risk due to her own medical issues. However, […]
Blogs
We All Know A Chair
Updated on February 9, 2022Written by Amy Breen, a patient of The Feingold Center for Children We all know a chair. We’ve encountered that chair various times. I know I have, sometimes to get […]
Blogs
“Everything Seemed Fine.”
Updated on February 9, 2022Charlotte Couldn’t Feed Without Choking When Jenna gave birth to her second child, Charlotte, in September 2014 at Lowell General Hospital, “everything seemed fine,” she explained. However, Jenna discovered that […]
Blogs
“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 […]
News
100% Match For Your Donation Before Sunday, August 22
Updated on February 9, 2022Double your impact and donate before Sunday, August 22, 2021. Your support is needed to continue our mission and further the legacy of Dr. Feingold. Please donate today to fund […]
Blogs
Getting A Diagnosis Was Life-Changing
Updated on February 10, 2022When 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 […]
Blogs
Explosion in Medical Knowledge Doesn’t Make It Easier for Affected Families
Updated on February 10, 2022Learn 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 […]
Blogs
Patient Continues Dr. Murray Feingold’s Legacy
Updated on February 9, 2022Tom 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 […]