About I AM ALS
I AM ALS is a patient-centric movement revolutionizing how to end disease. The nonprofit provides critical support and resources to people with ALS, caregivers, and loved ones. We empower advocates to raise awareness and lead the movement against ALS in driving the development of treatments and cures. Founded in 2019 by husband and wife team Brian Wallach and Sandra Abrevaya, I AM ALS was born out of their desire to rewrite the ALS story for Brian and the tens of thousands of other people with ALS. Learn more at www.iamals.org.


Industries
Entertainment & Media
Film and Motion Picture

Contact Information
MEDIA CONTACT:
Shawna N. Prince
Director of Communications & Marketing
872-529-1873
[email protected]

Latest

May 22, 2024, 09:02 ET I AM ALS Hosts Inaugural Community Summit and 3rd Annual Flag Event in Washington, DC for ALS Awareness Month

I AM ALS – a nonprofit movement supporting and mobilizing people impacted by Amyotrophic Lateral Sclerosis (ALS) – kicks off its first ALS Community...

May 06, 2024, 17:03 ET INSPIRING AND HOPEFUL DOCUMENTARY ABOUT I AM ALS CO-FOUNDERS AND REVOLUTIONARY COMMUNITY STORY WILL STREAM ON PRIME VIDEO

I AM ALS announced today that the film documenting its co-founder's fight and the revolutionary movement they built to end ALS will soon be streaming ...

Nov 23, 2022, 14:44 ET I Am ALS and Veterans with ALS send an Open Letter to FDA Requesting an Advisory Committee Meeting to Discuss NurOwn

To the Honorable Dr. Robert Califf and Dr. Peter Marks: We represent Veterans with ALS who support Brainstorm Cell Therapeutics' request for the FDA...

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