Epidermolysis Bullosa is a rare collagen disorder, and Debra of America is dedicated to helping families affected by it, raising awareness, and funds for research. I am part of their Youth Leadership Committee, which is super exciting! We'll be working together in the future and doing a lot with body image and self esteem, which is something I'm incredibly passionate about. You can read an interview I did with them here, and head over to their website here to see the great work they're doing for the community. 

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