HEALEY ALS Platform Trial Q&A
VirtualJoin us for a HEALEY ALS Platform Trial Q&A Our investigators and study team will be available to answer any and all questions that the you might have about the […]
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HEALEY ALS Platform Trial Q&A
VirtualJoin us for a HEALEY ALS Platform Trial Q&A Our investigators and study team will be available to answer any and all questions that the you might have about the […]
Making an Impact on ALS Advocacy in Your Community
VirtualJoin our upcoming Virtual Event: Making an Impact on ALS Advocacy in Your Community, on Wednesday, January 13, 2021, at 1:30 p.m. (Pacific). Request an invitation and RSVP here.
HEALEY ALS Platform Trial Q&A
VirtualJoin us for a HEALEY ALS Platform Trial Q&A Our investigators and study team will be available to answer any and all questions that the you might have about the […]
COVID-19 Vaccines Update: FDA and CDC Leaders Address the Rare Disease Community
VirtualThe National Organization for Rare Disorders (NORD), along with The ALS Association, Cystic Fibrosis Foundation and Muscular Dystrophy Association, is pleased to host a special webinar with leaders from the […]
NEALS Webinar: Expanded Access to Investigational Drugs
VirtualExpanded Access to Investigational Drugs Friday, January 15, 2021 4:00 - 5:00 PM EST Join us for a webinar on Expanded Access Programs (EAPs). In EAPs people with ALS who are […]
HEALEY ALS Platform Trial Webinar: Pridopidine, Mechanism of Action and Science
VirtualJoin us for a HEALEY ALS Platform Trial Webinar, "Pridopidine, Mechanism of Action and Science" with representatives from Prilenia, who will discuss Pridopidine, which is Regimen D in the HEALEY […]
Webinar – ASK ME: ALS Research and Care in 2021
VirtualASK ME: ALS Research and Care in 2021 Please save the date and join us with your coffee and breakfast on a Saturday morning! This informative event will feature leading […]
HEALEY ALS Platform Trial Q&A
VirtualJoin us for a HEALEY ALS Platform Trial Q&A Our investigators and study team will be available to answer any and all questions that the you might have about the […]
My ALS Communication Passport to Quality Care with Karen Steffens, RN, CHPN, CCM
My ALS Communication Passport to Quality Care is a tool for individuals living with ALS and their families. The 12-page Passport document, which is available in hard copy and online, […]
The Hermstad Legacy: Advances in Treatments for ALS
VirtualOn February 4th, we invite you to join special guest and ALS research advocate Ben Stiller, foremost ALS clinicians, leading researchers, and dedicated patient advocates to learn how Jaci and Alex […]