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White Waves

Meet H&M Role Model
A V E R Y  J O Y

THIS RARE BIRD IS A DANCING QUEEN

Avery Joy and her Mama, Abbey, tirelessly advocate for the inclusion of children with disabilities. That's why even though she uses a wheelchair, Avery Joy gets on stage and dances her heart out. She reminds us that we can find joy and belonging, no matter the differences we see on the outside.

 

Avery, Abbey, and their friends at Rare Birds Foundation are searching for treatments that can slow the progression of Avery's rare disorder, ADSL Deficiency, which is life-limiting and currently has no treatment or cure. 

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Please follow the link below to donate to research that will lead us to a treatment and keep Avery Joy dancing for years to come! 

Shop Abbey's collection of books for children teaching inclusion and disability acceptance!
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About Rare Birds Foundation

for ADSLD

Rare Birds Foundation came together in 2023 to serve patients and families affected by ADSL Deficiency Disorder, a rare genetic disorder of purine metabolism. 

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Our Mission:

  • Find Treatment Options

  • Find a Cure

  • Support Families Affected by ADSLD

  • Raise Awareness and Increase Access to Testing

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Follow us on our Socials​

  • Facebook
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  • LinkedIn
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FIND OUT MORE

Togetherness

NEWLY DIAGNOSED?

You are not alone. 

Find ways to connect with your community and be 'rare together'. 

DNA

RESEARCH

There are teams around the globe doing research on this rare disorder. 

Donation Jar

SUPPORT US

Our all-volunteer organization needs your support. 

WHERE WE ARE

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