A mother’s narrative of sorrow and superstition unfolds in a rural community set among the scenic mountains of Apayao, Philippines, wrapped in the mystery of a rare medical illness known as ‘werewolf syndrome.’ Alma, a dedicated mother, describes her journey of worry, remorse, and, eventually, hope as she deals with her son Jaren’s unusual and perplexing condition.
Jaren Gamongan, now two years old, was born with a unique feature: a full head of hair, black sideburns, and patches of hair covering his face, neck, back, and arms.
Alma and the townsfolk were both perplexed by Alma’s unusual look, which resembled a mythological werewolf. However, beneath the mythology and superstitions lies a deeper, more painful story.
Alma recounts her pregnancy, which was characterized by excessive desires for wild cats, a delicacy popular in the hilly region where she lived. Desperate to fulfill her appetite, she gave in to superstition and tradition, believing that eating a wild cat would satisfy her needs while also protecting her pregnant child. She had no idea how serious the ramifications would be.
Alma’s worst worries were realized when Jaren was born, as he showed clear evidence of ‘werewolf syndrome.’ Consumed with sorrow and remorse, she struggled with the idea that her actions during pregnancy had cursed her kid. The stigma and traditions surrounding their town only added to her misery, leaving her feeling alienated and alone in her struggle.
Understanding ‘Werewolf Syndrome’
Hypertrichosis, sometimes known as ‘werewolf syndrome,’ is a rare medical disorder marked by abnormal hair growth on various parts of the body that exceeds the normal range for age, race, and gender. This ailment, which can be present at birth or emerge later in life, affects only a small number of people globally, making it a medical anomaly of great curiosity and mystery.
Contrary to popular belief, hypertrichosis is not caused by elevated amounts of male hormones, but by hereditary traits acquired from one’s parents. The illness provides distinct physical and mental obstacles for people affected, frequently resulting in social shame and psychological misery.
We develop a deeper understanding and empathy for people like Jaren and his family by bringing light on ‘werewolf syndrome’ and the difficulties that folks with hypertrichosis endure. Through education, advocacy, and support, we can help these people embrace their differences and navigate life with courage and dignity.
