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.
Resiliency
Unleashing the Power of Self-Compassion: A Resolution to Suffer Less
Updated on February 25, 2022By 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 […]
Resiliency
Gaining Control with Gratitude
Updated on February 25, 2022By Laura Will Reprinted with permission from www.Knowrare.com It was 3am, and I could not sleep. We had just been told that our 4-month-old son’s brain had “folded wrong” in […]
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
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 […]