Body Bizarre Season 7 Episode 7 My Twisty, Upside-Down Body

Body Bizarre is an awe-inspiring series that delves deep into unique, strange and unusual anomalies of the human body. In this episode, titled My Twisty, Upside-Down Body, viewers will be introduced to individuals who are dealing with extraordinary conditions that are challenging both physically and psychologically.

The episode begins by introducing us to Evan, a young boy from the United States, who was born with a rare condition called visceral heterotaxy. Visceral heterotaxy is a condition where the organs of the body grow in the wrong place, leading to various medical complications. Evan has a twisted and upside-down colon, which has led to multiple surgeries, hospitalizations and near-death experiences. Doctors have told Evan's family that the chances of him living to see adulthood are slim due to the severity of his condition. Despite the odds stacked against him, Evan has a determined outlook on life that inspires everyone he meets.

The next person we meet is Aaryan, a teenager from India who suffers from a rare genetic disorder called Marfan syndrome. Marfan syndrome affects the body's connective tissue, causing the bones to grow longer than usual. As a result, Aaryan has elongated limbs and fingers that make him stand out in a crowd. As a child, Aaryan was bullied and marginalized because of his physical appearance, but he has now learned to embrace his body and is living life to the fullest.

Viewers will also meet John, a man from the United Kingdom who was born with an incredibly rare condition called Poland syndrome. This condition affects the development of muscles on one side of the body, making one arm smaller than the other. John's particular case is so unusual that doctors initially thought he had cancer. John has faced numerous challenges because of his condition but has never let it hold him back. He has become a fitness enthusiast, inspiring others to embrace their differences and stay fit.

The episode also introduces us to Mariana, a young woman from Mexico who spent the first few years of her life fighting for survival. Mariana was born with a rare condition called Harlequin ichthyosis, a genetic disorder that affects the skin. Babies born with Harlequin ichthyosis have skin that grows up to ten times faster than normal, leading to thick and scaly skin. The condition makes it difficult to regulate body temperature and can lead to infection. Mariana's parents were told she wouldn't survive past the first few days of her life, but she is now a thriving teenager who has learned to embrace her condition and wants to become a doctor to help others.

The final person we meet is Mark, a man from the United States who has lived his entire life with an extremely rare condition called pectus carinatum. Pectus carinatum is a condition where the chest bone protrudes outward, causing the chest to look like it has a second set of breasts. As a child, Mark was ashamed of his condition and was teased relentlessly by classmates. However, as he grew older, he learned to accept his body and has since become a successful model. Mark now hopes to inspire others to embrace their unique qualities and live without fear of judgment.

My Twisty, Upside-Down Body is a heartwarming episode that showcases the resilience and strength of the human spirit. Each of the individuals featured in this episode has faced incredible adversity, but they have all refused to let their conditions define them. Instead, they have chosen to embrace their differences and live life to the fullest, inspiring others to do the same. This episode is a testament to the power of the human will and is sure to leave viewers feeling inspired and uplifted.