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Andrew was born with a rare genetic disease called Duchenne Muscular Dystrophy. DMD is a progressive terminal muscle wasting disease for which there is no cure currently. Right now it is weakening his arms, heart, and lungs, and is rapidly robbing Andrew of his ability to walk. It is a cruel disease but “Little” is a bright, spirited, wild thing and he doesn’t let his condition snuff out his fire one bit.

Andrew has been loved and covered in prayer his entire life by so many people. We are continuously blown away by the generous and caring hearts of the people around us. We call our supporters “Little’s League” and we cherish every one of you.

Updates (1)

June 22, 2021

We had such a great time at “Pound for Andrew” last night and thanks to your generosity, over $4400 was donated and will be deposited into this account shortly! I cannot thank you enough! Stay tuned for more fundraising events coming soon and check out the Pound album for pics of last night.

Photo Galleries (4)

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June 23, 2021

We miss you buddy!

Scott Adams

June 22, 2021

For Andrew Palmer and his sweet mother, Katherine!

Shea Siler

June 22, 2021

God bless you Andrew! Want to help you get your much needed van! Love, Cuzn Kathy

Kathleen Jones

June 21, 2021

We love you guys so much!! Continued prayers for sweet Andrew! Love, Justin, Claire, Kaitley and Eli

Claire Powell