Be a light of hope this holiday season. Ignite more progress, restore more freedom, and inspire more hope for families living with neuromuscular disease.

#Drive2DoMore for MDA Families with Jiffy Lube

Visit a participating Jiffy Lube service center and help transform the lives of children and adults with neuromuscular disease.

Make a Donation Find a Participating Service Center
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Visit a Participating Jiffy Lube Today and Drive2DoMore!

When you visit participating Jiffy Lube Service Centers during the month of August, you can Drive2DoMore and support the Muscular Dystrophy Association’s unparalleled services, including medical care at over 150 clinical care centers and world-wide therapeutic research.

With a donation of $3 or more, you will receive a Drive2DoMore savings book of Jiffy Lube discounts.

Thank you, Jiffy Lube, for 10 years of support as you #Drive2DoMore for the neuromuscular community!

Since launching its first fundraising campaign for MDA 10 years ago, Jiffy Lube has raised more than $7 million to support research, care and educational programming – all making impacts for families living with neuromuscular diseases.

"At Jiffy Lube, we understand the importance of mobility, and through the Drive2DoMore initiative, we are honored to work alongside MDA so those living with neuromuscular disease can participate more fully in their communities,” said Sara Smith, Director of Marketing for Jiffy Lube International, Inc. “It’s incredible to see the impact that our long-standing collaboration has had on driving life-changing research, and together with Jiffy Lube franchisees and customers, we are committed to do more for the MDA families in their communities."
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Meet MDA's Ambassadors

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    Meet Maddee, MDA's Ambassador of Louisiana

    “I’m so happy to be part of the Jiffy Lube campaign, because it is raising awareness about muscular dystrophy that I live with.  It’s important to me, that people understand we need to raise money so we can get care and new treatments to help us live our lives.”

    Meet Maddee. She loves dancing and even had the opportunity to create a touch down dance with Kelly Rowland for her brother who plays in the NFL! Maddee was born with and lives her best life with Congenital Muscular Dystrophy (CMD). By participating in MDA Summer Camp and other events, Maddee has met a wide range of awesome people who truly appreciate her larger-than-life personality, she exudes confidence and has a deep desire to help others in our community.

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    Meet Ethan, MDA’s National Ambassador

    “MDA’s support has allowed me to have access to the care I need to live my life. Thanks to your support there are more breakthroughs to come, if we all drive to do more together!”

    Meet Ethan. Ethan is diagnosed with Duchenne Muscular Dystrophy (DMD). He is currently serving as MDA’s National Ambassador, meeting with MDA partners and sharing his story. MDA Summer Camp has helped Ethan as he navigates new challenges, like getting a wheelchair, because he has seen his friends from camp use wheelchairs as well. MDA helps Ethan’s family feel like they are not alone in this journey, and he has continued to make us all laugh with his Joke A Day for MDA campaign to raise awareness, and make people smile!

  • A picture of Jordan.

    Meet Jordan, MDA's Ambassador of Minnesota

    “I’m always happy to share my story living with muscular dystrophy so people understand what I’m going through, and how they can help MDA support the care I need.”

    Meet Jordan. He dreams of his future employment at his favorite store, and volunteers to help medical students learn about the neuromuscular disease he lives with, spinal muscular atrophy (SMA). He has had to overcome obstacles all his life and has adapted well. He does not let his disease define him and his love for life is undeniable. Everywhere he goes he makes a new friend and is well known in his school and community.