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Tayma Salim: Dystrophic

Tayma is 8 years old and was diagnosed with Dystrophic Epidermolysis Bullosa at birth. Her journey has been very long and hard for our family, but despite the trials she faces, Tayma has a vibrant spirit and continues to approach life with the spirit of any other young girl, full of dreams and aspirations. 

Tayma dreams of becoming famous one day and shares her passions through her Instagram account (Tayma_usa), where she shares cooking videos and makeup tutorials with her followers.

Tayma is a social butterfly. She loves being surrounded by friends and loved ones, meeting new people, and making friends at school. 

One of Tayma's biggest dreams is to become a doctor. Inspired by her experiences, she hopes to help others and make a difference in the medical field, just as her own outstanding doctors are doing for her.

As Tayma grows older, her symptoms may progress, but her family’s love and support, combined with her doctors’ care and her own determination, help us face each day with courage and optimism.

- Laalej Family 


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  • Epidermolysis Bullosa
    • What is EB?
    • Life with EB
    • Resources
  • Research
    • Our Impact
    • Scientific Advisory Board
    • Clinical Trials >
      • Filsuvez
      • Vyjuvek
      • ZEVASKYN
    • Town Halls
    • Apply for a Grant
  • Get Involved
    • Donate
    • Sponsor
    • EB Active
    • Events
    • The Effect
    • Shop
    • Give Cryptocurrency
    • Give Stocks
    • Give through Donor Advised Funds (DAF)
    • Accelerator Fund
  • Media
    • Matter of Time Film
    • Press
    • Videos
  • About Us
    • Our Mission
    • Financials
    • Venture Philanthropy
    • Supporter Spotlights
    • Leadership >
      • Board of Directors
      • Staff
  • Donate