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Parent Project Muscular Dystrophy invites you to attend:Addressing Lifelong Care Needs in Duchess Muscular Dystrophy With Leslie Vogel, PT, MS Seattle Children's Hospital & Tina Dong, PT, MPT Stanford
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Who needs parent project muscular dystrophy?

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Parent Project Muscular Dystrophy benefits individuals and families affected by muscular dystrophy.
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Anyone who has a loved one with muscular dystrophy or believes in supporting research and advocacy for this condition can contribute to the parent project.
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Patients, caregivers, medical professionals, and anyone interested in finding a cure or improving the quality of life for those with muscular dystrophy can benefit from the services and initiatives of Parent Project Muscular Dystrophy.
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Parent Project Muscular Dystrophy (PPMD) is a nonprofit organization focused on finding a cure for Duchenne muscular dystrophy.
Individuals, families, and organizations interested in supporting research and advocacy for Duchenne muscular dystrophy.
You can fill out the form on the PPMD website or contact them directly for more information on how to get involved.
The purpose of PPMD is to accelerate research and support programs to end Duchenne muscular dystrophy.
Information on fundraising activities, research progress, advocacy efforts, and impact on the Duchenne community.
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