An MDA Summer Camp Love Story

Looking back, neither one of us went to camp expecting to meet the person we’d one day marry. … I can’t imagine my life without Zach. We can’t imagine our lives without our camp family or MDA Summer Camp.

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Ethan Lybrand, MDA Summer Camp, and His Wheelchair Named “Bumblebee”

Ethan Lybrand loves his Bumblebee. On Oct. 27, the 7-year-old became the proud owner of his first power wheelchair. Black and yellow, the chair’s color scheme is inspired by, and named after, his favorite Transformers character, Bumblebee. For Ethan, who has Duchenne muscular dystrophy, getting a wheelchair could have been a tough transition. Instead, Ethan . . .

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Albertsons Companies Employee Lives Unlimited at MDA Summer Camp

Albertsons Companies Employee’s Daughter Develops Connection for MDA Summer Camp As the second-largest grocery retailer in the country, Albertsons Companies and the Albertsons Companies Foundation, continue to show their passionate support of the Muscular Dystrophy Association (MDA) across the country for over 20 years through in-store fundraising campaigns with their customers, partnering with Acosta Sales . . .

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Why I Walk: For Community, Camp and Cures

  Editor’s note: The following is adapted from a letter Stephanie Hoover wrote to family and friends to ask them to support her in the Louisville Muscle Walk. We thought her characterization of the impact of her disease and her eloquent description of the community she has found within MDA were worth sharing. We hope you . . .

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ERA Helps Hundreds of Kids Have the “Best Week of the Year” at MDA Summer Camp

For more than 35 years, ERA Real Estate has been committed to enriching the lives of children and adults living with Muscular Dystrophy and other neuromuscular diseases through its support of MDA. In particular, the ERA network has been helping kids living with muscular dystrophy, SMA and related muscle-debilitating diseases have “the best week of the . . .

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From MDA Camper to MDA Staffer: An MDA Double Life

For the past seven months, I have been working at the Muscular Dystrophy Association’s National office in Chicago. This is my first job since graduating from college (I attended Illinois State University and graduated with a degree in broadcast journalism in May 2015), and it truly has been an eye opener. For starters, the people . . .

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MDA Summer Camp Celebrates 60 Years of Changing Lives

Barrier-free, weeklong camp for kids with neuromuscular disease offers ‘Awesome Adventures’ CHICAGO, May 20, 2015 – The Muscular Dystrophy Association (MDA) is set to kick off another season of summer camp. Now in its 60th year, MDA summer camp supports families by hosting thousands of kids fighting muscular dystrophy and other life-threatening diseases that severely . . .

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