
Body Bizarre
BODY BIZARRE traverses the globe, uncovering stories of people with rare anomalies. Some of these conditions have left the medical world baffled, while others require surgery so intricate and demanding that the odds of survival are minimal at best. Each hour-long episode takes viewers behind the headlines to shed light on what life is like for the incredible individuals who live with these afflictions, from being born with an extra-long neck to having sideways feet. Through personal interviews and a look at the science behind their ailments, BODY BIZARRE provides a diverse perspective of the unknown while unveiling humanity at its best.
- 2013-2025
- 8 seasons
- TLC
- Documentary, Reality
- TV-14
BODY BIZARRE traverses the globe, uncovering stories of people with rare anomalies. Some of these conditions have left the medical world baffled, while others require surgery so intricate and demanding that the odds of survival are minimal at best. Each hour-long episode takes viewers behind the headlines to shed light on what life is like for the incredible individuals who live with these afflictions, from being born with an extra-long neck to having sideways feet. Through personal interviews and a look at the science behind their ailments, BODY BIZARRE provides a diverse perspective of the unknown while unveiling humanity at its best.
Season 8 Episode Guide
10 Episodes 2025
Episode 1
Born as One Sister
Wed, Mar 4, 2026 42 mins
In California, conjoined twins Erika and Eva Sandoval undergo a 17-hour surgery. In Mississippi, Wells Middleton battles through his new future after losing both his hands. In Indonesia, Andriadi Putra has over 30kg of tumours on his body.
Episode 2
The Worst Disease You've Never Heard Of
Wed, Mar 4, 2026 42 mins
In Staten Island, New York, 15-year-old John suffers from epidermolysis bullosa and has no indication of how long he might live. In Kansas City, 28-year-old Justice suffers from a rare sleep condition called chronic neurological disorder.
Episode 3
Tumors Forced My Eye Out
Wed, Mar 11, 2026 42 mins
Despite 22 surgeries and the loss of his right eye, Amit won't let incurable neurofibromatosis control his life. Nine-year-old Rajeshwari seeks treatment for her ichthyosis, while Mari Jade battles daily seizures.
Episode 4
Missing Half a Skull
Wed, Mar 11, 2026 42 mins
Three individuals face extraordinary medical challenges: Brandon undergoes skull removal surgery, Harper lives with a condition causing rapid skin growth, and Rafi recovers from a severe brain hemorrhage to rebuild his life.
Episode 5
Facial Tumors Won't Stop Growing
Wed, Mar 18, 2026 42 mins
In India, a man undergoes transformative facial surgery to remove massive tumors, while in California, a woman receives round-the-clock medical care to extend her life.
Episode 6
A Life Changing Accident
Wed, Mar 18, 2026 42 mins
Natalie, 18, moves forward with her life after surviving a devastating bonfire explosion that left her with severe burns. Meanwhile, 11-year-old Levi in Mississippi navigates life with a rare form of dwarfism.
Episode 7
I Have Vanishing Bones
Wed, Mar 25, 2026 42 mins
Natalia was born with a rare condition referred to as the 'vanishing bone disease'. Sanja has a condition that causes blisters to form on her skin. In Ohio, Tiffany, 41, was diagnosed with progeria when she was in her late twenties.
Episode 8
My Ankle Is My Knee
Wed, Mar 25, 2026 42 mins
After having her leg amputated, Jillian has surgery which will allow her to use her ankle as her knee. In Peachtree City, USA, Ashley Kurpiel suffers from a rare condition that turns her muscles to bone.
Episode 9
A Conjoined Life
Wed, Apr 1, 2026 42 mins
The family of conjoined twins, Callie and Carter, must decide whether to separate them. Abandoned by her birth mother and born with no arms, Deborah refuses to let her tragic early life hold her back. Josh shares his life as 'The Tourette's Barber'.
Episode 10
I've Broken My Bones Over 400 Times
Wed, Apr 1, 2026 42 mins
Both born with brittle bone disease, Dejua and Antwon have suffered over 600 breaks between them. Robert's spine is not connected to his hips. In California, Yesi, 35, was born with diastrophic dysplasia, a rare type of dwarfism.