Let's Cure ASMD with the Wylder Nation Foundation ~ Project For Awesome 2023

Neimann-Pick Type A is a form of ASMD that robs children of their minds and bodies until it eventually kills them. Join me in raising money to fund the life-saving treatment that is currently being produced to fight Acid Sphingomyelinase Deficiency. Money will expedite the research and get it to the kids whose lives absolutely depend on receiving treatment as soon as possible. Raising awareness of this rare genetic disease and its treatments is also an incredibly important part of this process. I hope we can be part of getting a cure to these sweet children so they can flourish. Photos of Damain are used with his mom's permission. Vote for my video on the Project for Awesome site: https://projectforawesome.com/watch?v=KtNoOCIficc&fbclid=IwAR1z3MSyLiNlxeIQ6p5OcB98QOw2XUnn97hR0qTUOGLM-gNcIFSeB3cxrzw Check out and donate to the Wylder Nation Foundation here:  https://wyldernation.org/ Follow Damian's story on IG:  https://www.instagram.com/pleasesavedamian/?hl=en On his mom's blog: https://www.savedamian.com/On Brittany Markham on Youtube:  https://www.youtube.com/@pleasesavedamian Check out Jillian Arnold's IG. She has two children with ASMD: https://www.instagram.com/confessionsofararediseasemama/?hl=en #P4A2023