Featured Fundraising Initiatives


Are you living in Massachusetts? If so, we hope you’ll DRIVE TO END ALS by getting the official Massachusetts ALS Charity License Plate. 100% of proceeds support critical research and care! Learn more about how you can get yours at: ALSplate.com

Featured Event


7th Annual ALS ONE Snow Ball Gala
January 29, 2022
7th Annual ALS ONE Snow Ball Gala
Our most magical and important event of the year will be back IN-PERSON and we hope you’ll join us on Saturday, January 29th, 2022 for our 7th Annual ALS ONE Snow Ball Gala! We couldn't be more excited to join with ALS families, friends, and supporters for a night of inspiration, fantastic food, top-notch entertainment, dancing, friendship, community, and an unsurpassed level of joy and hope as we celebrate the season and the many accomplishments despite a very difficult past year, while raising critical funds for ALS research and care.
January 29, 2022
Save the date for our most magical night of the year - our annual Snow Ball Gala! Our hope is to be able to once again hold this event in-person! We've got it booked for Saturday night, January 29th, 2022 at the Boston Marriott - Quincy and our fingers are crossed that the pandemic will be long behind us! Stay tuned for more information as the date nears.

Ongoing Support Initiatives

Take Action

A Little Something campaign

If you own or work for a business, you have the unique opportunity to offer employees a chance to give A Little Something™ to ALS ONE in the form of an ongoing payroll deduction. A little goes a long way, especially when we are so close to discovering effective treatments.

Unity makes us stronger. Will you be ONE with us?

Start your own fundraiser today to help benefit ALS ONE

Our founder, Kevin Gosnell, always said “If everyone would have just ONE fundraiser per year, just ONE, imagine what could be done? Imagine the difference we could make.”

Will you be the next one to host a fundraiser? Contact us and we’ll help you create a great fundraiser that’s fun for you and crucial to ALS ONE. Please email Jen DiMartino to learn more about getting involved.

Press & News

Healey ALS Platform Trial Update
The latest updates on The Healey ALS Platform Trial were provided via zoom webinar on 7/7/20. This hour-long informative session by Dr. Merit Cudkowicz and team includes many answers to frequently asked questions by pALS and families.
MDA grants ALS ONE $750,000
MDA and ALS ONE form new partnership to accelerate ALS biomarker research