Next generation treatments are here NOW

Help keep ALS research on the fast track! [Help keep ALS research on the fast track!]( [View Online.]( [MDA]( [Donate Now]( May is ALS Awareness Month [Progress accelerates every time you give - Help MDA raise $300,000 by May 31]( Dear {NAME}! ALS is a tough enemy. It does not discriminate. It can strike adults at almost any age. It’s almost twice as likely to arise in fire fighters and members of the military. It affects men and women of all races and ethnic backgrounds. And as of today, there’s still no cure. [But as tough as this enemy is, the MDA community is tougher.]( Thanks to your support, scientists are steadily learning more about how ALS works and translating those discoveries into new treatments. [ALS Progress 101]( {NAME}, this next generation targeted therapy is here NOW, and it’s giving people with ALS more quality time with their loved ones. But we can’t let up. ALS moves too quickly and too many lives are at stake. We can’t stop until there’s a targeted treatment for every genetic culprit. We can’t stop until there’s a CURE. [Please give generously during ALS Awareness Month to keep critical research and groundbreaking treatments on the fast track!]( Gratefully, Donald S. Wood, PhD President & CEO, Muscular Dystrophy Association [Give Now]( [MDA]( [Donate Now]( [Facebook]( [Twitter]( [YouTube]( [Instagram]( [LinkedIn]( [MDA.org]( © 2024 Muscular Dystrophy Association, Inc.. All rights reserved. 1016 W Jackson Blvd #1073 Chicago, IL 60607 1-800-572-1717 State Fundraising Notice The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization. [View Online]( | [Privacy Policy](