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Brian Wallach is an American businessman, lawyer, and amyotrophic lateral sclerosis (ALS) research and patient advocate. He became known for his activism after being diagnosed with ALS in 2017. Since then, Wallach has founded a nonprofit, I AM ALS, and a telemedicine company, Synapticure.
5 juin 2024 · NPR's Juana Summers checks in with Brian Wallach, who has been living with ALS for seven years, and his wife Sandra Abrevaya on their ongoing advocacy for ALS patients, families and caregivers.
5 juin 2024 · Brian Wallach is a former White House counsel who was diagnosed with ALS at 37 and fought for more funding and access for research. His story and his wife Sandra Abrevaya's are featured in a Prime Video film, For Love & Life: No Ordinary Campaign.
- Kate Hogan
30 juin 2023 · Sitting in his wheelchair, 42-year-old Brian Wallach looks out over the park, rooting for a very particular outcome that has nothing to do with baseball.
Founded by ALS patient Brian Wallach and his wife, Sandra Abrevaya, I AM ALS is revolutionizing how we cure ALS by empowering and mobilizing patients, engaging with policy-makers and offering vital resources for people impacted by ALS.
Founded by ALS patient Brian Wallach and his wife, Sandra Abrevaya, I AM ALS is revolutionizing how we cure ALS by empowering and mobilizing patients, engaging with policy-makers and offering vital resources for people impacted by ALS.
14 janv. 2022 · Brian Wallach was diagnosed with ALS in 2017 and given six months to live. He used his time to change how medical research and advocacy work for ALS patients, securing historic funding and access to treatments.
