Life at three foot tall: Woman with rare dwarfism defies trolls by becoming TikTok star

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 has also stunted her growth, which impacts several areas of her life, with doctors believing Isabella would never walk – but she has "proven them completely wrong".

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