Human motor neurons viewed with spinning-disk confocal microscopy

Student-founded · Funding ALS research

Moving ALS
research
forward.

We are high school students in Indiana and Arizona raising money for ALS research and patient care. Every donation goes to the ALS Therapy Development Institute.

$25,399

raised for ALS research

The total includes research grants and funding for patient care, not just individual donations.

Research grants
Funding secured for ALS research programs.
Patient care funding
Money for the care of people living with ALS.
Community fundraising
Events and individual gifts, like the pickleball tournament.

Partners

ALS Therapy Development Institute
Chipotle
Current Publishing
Society for Science
American Junior Academy of Science
Troy Times

Interview

Thirteen years inside ALS research.

Recorded over a video call in September 2026.

Alan Premasiri runs clinical research operations at the ALS Therapy Development Institute. We asked him what has changed in the field since 2013, what the public gets wrong about ALS, and what the community needs from people outside the lab.

Eight questions, 27:49.

Regeneron ISEF 2025

We won first place at ISEF.

Our PT150 project won first place in Computational Biology and Bioinformatics at the 2025 Regeneron International Science and Engineering Fair. The video is from the awards ceremony.

The Regeneron ISEF 2025 Grand Awards ceremony, at the moment our category was called.Society for Science on YouTube
Samarth Dunakhe standing beside the NeuroGraph research poster on ALS biomarkers at the American Junior Academy of Science meeting
The poster

Presenting at AJAS in Phoenix.

Samarth presented the project at the American Junior Academy of Science in February 2026.

Read the research →

Fundraiser recap

The pickleball tournament was a great success.

The full recap →

Twenty-four players at Gilbert Regional Park raised $120 for ALS research.

Phone footage from the tournament on August 15.
All nine photos and the recap →

New · White paper, August 2026

The year before a diagnosis.

In the United States, people with ALS wait ten to sixteen months between their first symptom and a diagnosis. Median survival is two to five years. Our white paper looks at why the wait is so long and what local groups can do to shorten it.

10–16 mo
from first ALS symptom to a confirmed diagnosis in the United States.
60%
already fail ALS clinical trial criteria on the day they are diagnosed.
$47,000
in medical costs during the first year after diagnosis, before anything a family pays out of pocket.

From the founders

We started ALS Forward to keep working on ALS after the science fair.

We’re Aryav and Samarth, high school seniors in Indiana and Arizona. Our research on PT150 won first place in Computational Biology and Bioinformatics at Regeneron ISEF 2025.

We are still doing research, and we raise money for the ALS Therapy Development Institute, which uses it for lab work on ALS treatments and for patient care.

Where your gift goes

Donations go directly to ALS TDI, which processes the payment and sends your receipt.