Take a look around our website to learn more about Taylor, Histiocytosis, how to help and all of our past and upcoming events! If you have any questions please contact us at tryan@taylorshopefoundation.com.

Thank you for visiting our site!

"Just because Histiocytosis is rare doesn't mean that kids like me that have it don't matter. I just want everyone to know about Histio and to make people that are sick smile. " ~ Taylor


We have one goal... to help other "sick" children and their families, while raising funds towards  Histiocytosis awareness and research.