The best week of their lives is waiting

And you can help them get there [And you can help them get there]( [MDA - Muscular Dystrophy Association]( [Donate Now]( [Give them a chance to just be kids]( Dear {NAME}, Exploring nature. Making a glorious mess with crafts. Giggling with friends long after lights out. Do you believe those joys should belong to every child? If so, will you help me get hundreds of kids and young adults living with neuromuscular diseases to MDA Summer Camp this year — at no cost to their families? [I'll give today]( A shortfall is putting pressure on many essential Muscular Dystrophy Association (MDA) programs. We need friends like you to rally around so that we can give kids living with neuromuscular disease the chance to just be kids at MDA Summer Camp. 93% of parents said MDA Summer Camp increased their child’s confidence. It’s a week with benefits that last forever. [Will you help more kids and young adults get there?]( Grateful for you, [Jeremy Signature] Cheryl Edwards Muscular Dystrophy Association [I'll give today]( [Forward this email to a friend!]( [MDA - Muscular Dystrophy Association]( [Donate Now]( [Facebook]( [Twitter]( [YouTube]( [Instagram]( [LinkedIn]( © 2023 Muscular Dystrophy Association All rights reserved. Muscular Dystrophy Association 161 N. Clark, Suite 3550 Chicago, IL 60601, US | 1-800-572-1717 [Unsubscribe]( | [State Fundraising Notice]( The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization. [View Online]( | [Privacy Policy](