A New Normal for the Torres Family
Patient StoriesJacob Torres is a loving, animated boy, who his mom Jessica describes as beating to the sound of his own drum. He loves sports, he loves to be...
Jacob Torres is a loving, animated boy, who his mom Jessica describes as beating to the sound of his own drum. He loves sports, he loves to be...
Seven-year-old Astraea is a bright and bubbly girl who loves swimming and feeling the sun on her face. Born with a rare genetic mutation of the STXBP1...
On Friday August 21st, The Joe Andruzzi Foundation (JAF) partnered with Munroe Dairy to host the first ever Scoops of Kindness event, bringing the...
At just 11 months old, Everly was diagnosed with neurofibromatosis type 1 (NF1), a genetic disorder that can cause tumors to develop along nerves. For...
Alexandra Clithero is a teacher living in Southern Maine with her husband Brandon, their 10-year-old son Austin, and two black labs. In 2021, Alex was...
Sunday, August 16, was one to remember as 45 incredible athletes hit the pavement at the 54th ASICS Falmouth Road Race, proudly representing the Joe...
Ella Schwarz has always spent her summers in Falmouth, Massachusetts. The house where her family stays each year sits directly along the Falmouth...
Justin and Kiki Fossbender, father and daughter, have both been running since childhood. Justin, who had a father who was a runner, followed in his...
Let's be honest. Writing a will probably isn't on anyone's list of favorite things to do. It's one of those tasks that's easy to put off. Life gets...
At the Joe Andruzzi Foundation, we're fortunate to have supporters who show up for cancer patients and families in so many ways. Some make an...