Keeping it going with the art and spreading awareness for EB. I am also working on some special gifts for our lovely medical families and friends. Please visit them and give them your support, monetary to just educating others about Epidermolysis Bullosa. Through my art and gaming, I am sounding the siren to advocate for people living with or have family with EB. To learn about EB please visit
Debra-international.org.
https://www.tiktok.com/live/event/7509531116546900014?_r=1&enter_from=share_link&share_from_user_id=7383379706879345710
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