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{NAME}, this movie is groundbreaking ...

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mdausa.org

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MDA@comms.mdausa.org

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Tue, Sep 17, 2024 12:06 PM

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Good Bad Things tells a story that’s never been seen before! September is Muscular Dystrophy Aw

Good Bad Things tells a story that’s never been seen before! [Good Bad Things tells a story that’s never been seen before!]( [View Online.]( [MDA]( [Double Your Impact]( September is Muscular Dystrophy Awareness Month [Good Bad Things]( Groundbreaking film brings the world a new icon: a protagonist living with a neuromuscular disease Dear {NAME}, I’m thrilled to be inviting you to a special virtual screening of Good Bad Things on Friday, September 20, through Sunday, September 22. [When you get your tickets here, 25% of the purchase price will be donated to the Muscular Dystrophy Association (MDA) in honor of Muscular Dystrophy Awareness Month.]( Good Bad Things centers around Danny, a young man with muscular dystrophy who is disillusioned by failed relationships. He finds the courage to step out of his comfort zone … and into the world of online dating, where he is matched with Madi. This unexpected connection challenges him to be vulnerable and sparks a profound journey of self-acceptance. Slowly but surely, Danny discovers the extraordinary beauty of his unique body. It’s amazing to see a team of producers and actors, including some who belong to the disability community, bring to the big screen a genuine, moving portrayal of life with muscular dystrophy. This is groundbreaking because authentic representation MATTERS. All people living with disabilities benefit from being shown as protagonists. That is what Good Bad Things brings to the table: an honest — beautiful — story about one man’s experiences while living with muscular dystrophy. [“It’s just a beautiful story of friendship and love and the things that we deal with, with a disability.” — Danny Kurtzman - Star of Good Bad Things, living with facioscapulohumeral muscular dystrophy (FSHD)]( Danny says on the movie’s theme: “As a disabled individual in today's world, we can control what we want out of our lives. We are in the driver's seat, and we have the power to write our own story.” [After hearing Danny’s powerful voice, I hope you’ll consider giving a gift of $35 or more to get your special MDA T-shirt and create even more awareness in your community about the real stories and experiences of people with muscular dystrophy.]( [Mindy Henderson] [Mindy Henderson] Mindy Henderson Vice President, Disability Outreach & Empowerment [Give Now]( [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](

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