News & Publications
ALS at any age is devastating, but when Dave was diagnosed in the Summer of 2023 at age 44, our children were just 13 and 10. Obviously, you can’t pause…
In the summer of 2022, several months after my husband’s legs didn’t seem to work anymore, we learned that they suspected he had ALS. I recall one day, soon after I…
When my dad was diagnosed with ALS at 73, he was the most active human I knew. He had the energy to live life to its fullest—on top of being…
On November 11 at Pier Sixty, ALS United Greater New York hosted its annual Lou Gehrig Legacy Gala, bringing together supporters, advocates, and leaders in the ALS community for an…
In early spring, ALS United Greater New York partnered with Assemblyman Steve Stern and Senator Jessica Scarcella-Spanton to introduce the ALS Registry Legislation (A7845/S6413), a groundbreaking bill designating ALS as…
This is a story of love and caregiving – spoiler alert, not all stories of love and caregiving necessarily have completely happy endings. I’m Elliot, and in April 2022, my…
Publications
- Fall 2025 Newsletter
- Summer 2025 Newsletter
- Advocacy Newsletter July 2025
- Protect Medicaid Letter
- Spring Newsletter 2025
- FY 2026 Federal Funding Requests
- Cuts to NIH Letter
- 2024 Year in Review
- Fall 2024 Newsletter
- Summer 2024 Newsletter
- Medical Aid in Dying Memo of Support
- Spring 2024 Newsletter
- 2023 Year in Review
- Fall 2023 Newsletter
- Summer 2023 Newsletter
- Spring 2023 Newsletter
- 2022 Year In Review
- Fall 2022 Newsletter
- 2021 Year In Review
- Fall 2021 Newsletter
- Summer 2021 Newsletter
- Winter 2021 Newsletter
- Fall 2020 Newsletter
- Summer 2020 Newsletter