Life at three foot tall: Woman with rare dwarfism defies trolls by becoming TikTok star
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Isabella Lamanna, 19, from Ontario, Canada, works as a content creator and has just finished her first year of university, doing an undergraduate degree in psychology. The student was diagnosed with diastrophic dysplasia when she was a baby, a rare condition that is one of 400 types of dwarfism, affecting her cartilage and bone development. It ...
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Replying to @malawijay Correction: Vickie has pseudoachondroplasia! I apologize for the error ❤️ Peet Montzingo and his mom Vickie are a great reminder that families with dwarfism all look different. If you want to know more of their story, you can check out Peet’s newest book, “Little Imperfections: A Tall Tale of Growing Up Different” #EduTok #LearnOnTikTok #BookTok #family #disability
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