Lyza is living proof there’s more to life than SMA 💪

Double your impact for people living with neuromuscular disease. [Double your impact for people living with a neuromuscular disease.]( [View Online.]( [MDA]( [Double Your Impact]( [You have TWICE the power to help people like Lyza thrive]( Dear {NAME}, “MDA is one of the greatest support mechanisms that I’ve had in my entire life,” says Lyza. This 22-year-old trailblazer, who lives with spinal muscular atrophy (SMA), is determined to experience everything life has to offer. That courage was always within her — friends like you just helped her find it! [Today, you can provide TWICE the support for people like Lyza by joining our August Challenge. Any gift you give, combined with challenge funds, will double in impact!]( When you see what Lyza has achieved in spite of her limited mobility, I think you’ll be inspired to step up: Lyza’s Life Without Limits {NAME}, this is what real empowerment looks like! And it’s what makes our August Challenge so important — because MDA’s #1 goal is always to help more people like Lyza live longer and stronger. [Please give the most generous gift you can. Combined with August Challenge funds, it will make TWICE the life-changing impact today!]( Gratefully, [Alicia Dobosz] Donald S. Wood, PhD President & CEO [Double Your Impact]( [MDA]( [Donate Now]( [Facebook]( [Twitter]( [YouTube]( [Instagram]( [LinkedIn]( [MDA.org]( [MDA.org]( © 2024 Muscular Dystrophy Association, Inc. All rights reserved. 1016 W Jackson Blvd #1073 Chicago, IL 60607 1-800-572-1717 [Unsubscribe]( | [State Fundraising Notices]( The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization. [View Online]( | [Privacy Policy](