Remarkably, Akshaj remains blissfully unaware of his medical condition. To him, his oversized leg is a unique gift that he believes will empower him to become a superhero, a perspective that fills him with gratitude.
Unfortunately, societal discrimination and the fear of potential infection often compel people to keep their distance from Akshaj. His family harbors concerns about the potential for bullying as he grows older and ventures into the school environment.
Mr. Khadelwal, Akshaj’s father, recognizes that his son is still too young to comprehend the harsh reality of his illness, especially considering the absence of a cure for Klippel-Trenaunay Syndrome.
He shared, “My son is oblivious to his ailment. We’re hesitant to impart any distressing information. In his eyes, his larger-than-life legs are the key to his superhero dreams. He’s too young to grapple with the complexities of his condition, holding onto the belief that his substantial leg makes him a superhero. It’s a positive outlook we’re determined to foster.”
Despite seeking assistance from multiple hospitals in New Delhi, the Khadelwal family faces challenges, with medical professionals at Fortis Hospital expressing uncertainty about successfully treating Akshaj.
Klippel-Trenaunay Syndrome is a rare genetic disorder impacting blood vessel, soft tissue, and bone development. Dr. Krishan Chugh, head of pediatrics, elaborated, “KTS is a malformation primarily found in children, where veins aren’t properly developed. Akshaj experiences intestinal bleeding tendencies, and tests indicate irregular blood supply to the intestines, causing vein expansion and subsequent bleeding.”
Akshaj’s parents persist in their search for a cure, acknowledging the heartbreaking reality of witnessing their son’s suffering. Shruti, Akshaj’s mother, lamented, “We’ve consulted all available doctors in Delhi, yet a viable treatment remains elusive. His health is diminishing, his stature is decreasing, and the leg size continues to swell, a source of profound heartache.”
