Help Jen raise money

My personal message: I'm so proud to be a member of The Healey Center for ALS' inaugural Falmouth Road Race team - running 7 miles and raising funds to advance critical research towards a cure for ALS. I've been working at MGH in the Healey Center ALS for 6 months now after leading an ALS non-profit (ALS ONE) for 10 solid years.  Meeting with people living with ALS every day in our clinic at MGH and seeing the devastation first-hand is overwhelmingly heartbreaking - but the resilience I'm privileged to witness, as well as the unwavering support of the best multidisciplinary team - inspires me every second of every day. To be a part of the help at this level is just incredible.  

I tell you - I am not a runner - it's very hard for me to run 3 miles, let alone the 7 that I'll be running at this race on August 19th, but I'm doing it in honor of one of my BF's, Michelle (shown in the photo), all whom I've known who have been devastatingly lost to the disease - and all who are living while battling ALS now. Your support in donating to my annual fundraising means more than you could possibly imagine.  I humbly ask to please give what you can.  

Hugging you tight, with gratitude,

♥️ Jen

All of us at the Sean M. Healey & AMG Center for ALS at Mass General Brigham (MGB) are extremely proud to be an official charity team in the Falmouth Road Race.

Our runners are taking on the seven miles of the Falmouth Road Race to help us stay up and running! The Sean M. Healey & AMG Center for ALS is a non-profit located inside Massachusetts General Hospital and under MGB (EIN #04-3230035), and so many of the programs, services, and research initiatives that support individuals and families living with ALS rely heavily on philanthropic support from people like you. Every contribution - large or small - directly helps fuel compassionate individualized care, family support programs, groundbreaking research, and hope for a future without ALS.

What is ALS?
ALS (amyotrophic lateral sclerosis), also known as Lou Gehrig’s disease, is a progressive neurodegenerative disease that affects the motor neurons in the brain and spinal cord that control voluntary muscle movement. As these motor neurons degenerate and die, individuals experience worsening muscle weakness, loss of mobility, difficulty speaking, swallowing, and eventually breathing. Most individuals diagnosed with ALS survive just 2–5 years after diagnosis, and there is currently no cure.

ALS devastates lives quickly and unpredictably, affecting not only the person diagnosed, but also the loved ones and caregivers who walk beside them every day. Your support helps provide hope, real help, and groundbreaking research - and means the world to all of us.

A few examples of programs and initiatives at the Healey Center for ALS  that your donation impacts include:

GROUNDBREAKING ALS RESEARCH, such as:

 The Healey ALS Platform Trial - Launched in 2020, this renowned trial is a first-of-its-kind perpetual, multi-center, multi-regimen platform trial designed to test multiple investigational ALS treatments simultaneously. Renowned for its efficiency in reducing trial cost by 30%, decreasing the average length of the trials by 50%, increasing patient enrollment by 67%, and allowing faster identification of promising therapies, this trial is now on its 8th regimen. The Healey ALS MyMatch Initiative - Launched in 2025, this is the first early-phase, biomarker-driven ALS clinical trial program to optimize participant population matching and increase early therapy response signal detection. In just a year, the Healey ALS MyMatch initiative has grown from a nascent idea to a fully operational program with a robust portfolio of high industry engagement and strong pipeline of trials, rapid site expansion and historically high trial enrollment metrics.  

MULTIDISCIPLINARY TEAM APPROACH

 Our multidisciplinary team cares for every aspect of the ALS journey. During clinic visits, patients and caregivers have access to numerous specialists and support services all in one place, allowing for comprehensive, personalized care while recognizing how valuable time and energy are for individuals and families living with ALS. 

ALS PACT PROGRAM

 ALS impacts the entire family. We provide access to child psychologists on our ALS PACT Program (Parenting At a Challenging Time) team who are right here at MGH.  They help families communicate with children - toddlers through young adults - and support their coping with ALS-related changes in a parent or grandparent. 

ALS HOUSE CALL PROGRAM

 With ALS, it can be difficult to drive to Boston for many visits. Any person with ALS who lives in the eligible area may receive visits in their home (in addition to their clinic multidisciplinary visits!) by an MGH ALS RN or NP through our ALS House Call Program, helping ensure continued access to specialized care and support. 

Because the Healey Center for ALS is a non-profit organization, all donations are fully tax-deductible.

To donate to one of our runners or our team in general via your Donor Advised Fund or personal check, please email Jennifer DiMartino at jadimartino@mgb.org.

With immeasurable gratitude to The Falmouth Road Race, all of our runners, and to you and all who are so generously supporting our work by donating to support our work.

Visit the Healey Center at: Sean M. Healey and AMG Center for ALS

#EndALS #HealeyHope