Unbelievable Me

After contracting an acute case of bacterial meningitis when she was 15, Paralympian Veronica from Bologna, Italy, has decided to share her scars with the world in the hope of inspiring body confidence.

In Austin, Texas, despite being born with no legs, skateboarder Kanya is living her life to the extreme. Abandoned at the side of a road at just three months of age, she is now thriving and is pursuing her dream of becoming a successful actor and model.

25-year-old wrestler Zion from Ohio, born without legs, is battling to become a successful athlete on the world stage after a troubled start in life. Meanwhile, in Northern Carolina, Sabrina had grown used to being held back by her severe Psoriasis.

In Texas, cancer may have taken 43-year-old Tina’s nose, but it certainly hasn’t taken her fighting spirit. At first, Tina struggled with how she looked, but has now embraced her appearance and aims to inspire others.

In South Africa, Shrivani, who was told her rare skin condition would prevent her from ever starting a family, has proved the naysayers wrong. And in Idaho, in the US, Trisha, who has brittle bone disease.

Inspirational father of two, Ryan from Detroit, lives without limits, despite missing parts of both his arms and legs. Fully adapted to life without limbs, he has taken it upon himself to help other families in similar circumstances.

After contracting meningitis at a young age and losing both of her arms, make-up vlogger Tilly from County Durham is getting to grips with her new bionic arms, whilst in Guayaquil, Ecuador, social media sensation Victoria tries to further her ambitions.

Seren has Tourette syndrome, and in order to combat misinformation, the 18-year-old from Worcestershire in the UK has taken to social media to share educational and humorous videos of her condition.

Gabe from Utah was born without limbs, but uses dance as a way to express himself. As Gabe moves out of his family home, he finds the courage to come out to his adoptive parents.

Tiny teacher Megan, from New Jersey, is proving that size is a reason to hold you back, even though some of her year three students tower above her. Megan has an extremely rare form of dwarfism, and has gone through a difficult time at school herself.