My ‘Ninja Turtle baby’ boy was born with a shell — he’s my superhero…

James McCallum, a proud father has shared the remarkable story of his newborn son, who was born with a rare congenital condition that gave him a shell-like structure on his back, akin to a turtle’s shell. Despite the initial shock, James and his family have embraced this uniqueness with love and admiration.

James McCallum. Meet the baby who was left with a “turtle shell” growth on his back after being born with a rare skin condition – and was called a “little ninja-turtle” by his parents. See SWNS story SWSMnevus. James McCallum, 19 months, was born with a large mass covering most of his back – leaving both his parents and doctors baffled. His mum, Kaitlyn, 35, claims ultrasounds did not reveal anything before she gave birth to the tot on August 19th 2021, 6lbs 14oz, at Morton Plant Hospital in Clearwater, Florida, US. The new mum was “concerned” when she noticed scabbing and lumps on what she thought was a birthmark. Kaitlyn and her husband, Tim, 41, a medical staffing recruiter, waited months for a diagnosis as the mass grew into what looked like a large mole that covered most of James’ back. After two month and undergoing multiple consultations, little James was diagnosed with giant congenital melanocytic nevus – benign, tumour-like malformations resulting from faulty development of pigment cell. James’ parents were reassured the growth could be removed in a series of operations.

Clearwater, Florida, toddler James McCallum earned the nickname “little Ninja Turtle” from his parents due to a rare skin condition resembling a turtle shell on his back. Despite inconclusive ultrasounds, concerns arose when scabbing and lumps appeared on James’ back post-birth. The mysterious condition covered 75% of his back, growing rapidly, impacting his sleep and daily life.

Facing uncertainty, James underwent an MRI to assess internal growth risks, leading to surgery at 2½ months to remove the nevus. Fortunately, no internal growth was found. Post-surgery, parents Kaitlyn andTim discovered a supportive Facebook group, learning about potential side effects like itchinessConnecting with a specialist, they initiated tissue expansion in September 2022, injecting saline weekly to replace affected skin. Despite challenges, James is now happier, and his parents anticipate complete removal by summer, prioritizing his comfort over potential scarring.

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In an exclusive interview, James McCallum expressed his feelings of amazement and pride in his son, referring to him affectionately as his ‘Ninja Turtle Baby’. He shared, “When I first saw him, it was like meeting a superhero. His shell makes him unique, but it’s his spirit that truly makes him special.”

Despite the challenges that may lie ahead, James and his family are determined to provide their son with all the love, support, and care he needs. They have already received overwhelming support from their community, with messages of encouragement pouring in from friends and well-wishers.

As they embark on this journey, James McCallum and his family hope to raise awareness about their son’s condition and inspire others to embrace differences with compassion and understanding. For them, their ‘Ninja Turtle Baby’ is not just a child with a unique physical trait but a symbol of resilience and strength.

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