United In ALS research and care.

ALS ONE is an unprecedented partnership of ALS researchers, clinicians, and care providers who have joined forces to advance critical research towards a cure while simultaneously providing essential equipment and resources to individuals currently living with the disease.

No one is ever on the ALS journey alone.

Research

Research

A partnership of world-leading ALS researchers focused on a cure

Get Involved

Care

Providing care and essential resources for those who need it most

Fundraising

Fundraising

Critical funding is necessary to further our united research and care

Working together

With the strength of the most caring community, we advance research towards treatments leading to an ultimate cure for ALS while providing equipment and resources to individuals living with the disease now in order to ensure the very best support, access to treatment, and quality of life for them during their journey with the currently 100% terminal disease.

Recordings now available!

Recordings from all segments of our 7th annual ALS Research Symposium, which was held November 13-15, 2024, are now available via links on the Symposium website under each title. Whether you were able to join us but would like to rewatch, or if you missed it and are seeing the presentations for the first time, we know you’ll be inspired by hearing from over 50 speakers in total, all working towards a cure for ALS. A profound showing of brilliance, unity, collaboration, respect and kindness.

Click HERE to view.

ALS Research Publication Review Series

Review 5: “What do you think caused your ALS?” (Aired on 12/17/24)

Our 2nd review of two under the umbrella of AI in ALS Research, aired on December 17, 2024, spotlighting the publication entitled, “What do you think caused your ALS? An analysis of the CDC national amyotrophic lateral sclerosis patient registry qualitative risk factor data using artificial intelligence and qualitative methodology” with featured publication authors, Dr. Danielle Boyce, DPA, MPH, Principal Investigator, Real World Evidence at ALS TDI and Jamie Raymond, MPH, Epidemiologist at the CDC, along with panelists: Dr. John Novak, MD, Dr. Nadia Sethi, Brian Andre, and Jen DiMartino. This webinar features a poignant conversation about the analysis of an important survey that was completed by over 3,000 participants in the CDC and Prevention’s National ALS Registry who answered the question, “What do you think caused your ALS?”.

Click HERE to view the webinar.

Click HERE to read the publication.


Introducing the ALS ACE Initiative

Announcing a powerful new initiative to advance ALS research, of which we are a proud support partner! Together with the Sean M. Healey & AMG Center for ALS at Massachusetts General Hospital and the Les Turner ALS Center at Northwestern Medicine, we are thrilled to announce the launch of the Acceleration Centers of Enrollment (ACE) initiative: The ACE initiative aims to accelerate enrollment and operational improvements in ALS clinical research by increasing access to clinical trials, expanded access protocols, and non-therapeutic research studies. Support for the ACE initiative comes from an Anonymous donor, ALS ONE, and the Les Turner ALS Foundation.

The initiative will be led by a team of clinical investigators from both Mass General and Northwestern. The Mass General team will be comprised of Merit Cudkowicz, M.D., MS.C., Sabrina Paganoni, M.D., Ph.D., and Doreen Ho, M.D. Senda Ajroud-Driss, M.D., will lead the team at Northwestern. Between the two centers, the ACE initiative will provide funding for staff, training, and infrastructure to accelerate participation in research, ultimately broadening access to potential treatments and programs for people living with ALS.

“We need transformative initiatives to change the trajectory of ALS research and care,” said Dr. Paganoni. “With programs like ACE coming to fruition, we are forging new paths for those who desire to contribute to research and gain access to clinical trials, expanded access and other important studies.”

The HEALEY ALS Platform Trial has been a leader in pioneering innovation and advancing research in ALS. There is tremendous interest in participating in this study as well as other exciting research projects. The ACE initiative will improve access and efficiency, funding training and salaries of additional staff, and ultimately broadening access for people with ALS to potential treatments and programs.

“ALS ONE is honored to be a support partner of the Acceleration Centers of Enrollment (ACE) initiative. This innovative program will significantly enhance access to critical clinical trials and research studies for people living with ALS” said Jennifer DiMartino, Executive Director of ALS ONE. “ACE is a vital step towards faster, more efficient research and ultimately, finding treatments and a cure for ALS.”

Read the full press release about The ACE initiative HERE.

Events

24-Hour Picklethon for ALS Research & Care!
January 24, 2025
24-Hour Picklethon for ALS Research & Care!
Calling all Pickleball lovers! Join us for a 24-hour Picklethon for ALS starting on Friday, January 24th at 5PM through Saturday, January 25th at 5PM at Martini’s Indoor Pickleball & Athletic Club in Stoughton, MA! All ages and experience playing pickleball are welcome to pick a time slot or several during the 24-hour time frame.
SHIFSTRONG 3V3 HOCKEY TOURNAMENT
February 23, 2025
Shifstrong 3V3 Hockey Tournament
Register to play or come out to watch! Shifstrong 3V3 Hockey Tournament at at Gardner Rink St. Mark’s School in Southborough, MA. $25 per Hockey Player, $125 per Team $10 Free Skate. Schedule is on the website. Help us ICE ALS!
10th Annual SNOW BALL GALA
March 1, 2025
10th Annual SNOW BALL GALA
JOIN US or SUPPORT our 10th Annual SNOW BALL GALA! 2025's most exciting, important, and heartwarming night of the year to support ALS research as well as equipment for individuals living with ALS will be held at the Westin Seaport in Boston, MA! Tickets and Sponsorship are on sale now!! Tickets always sell out so don't delay!💚💙