Arya Permana, an Indonesian teenager who once weighed 421 lb (191 kg), was so big that he had to take showers outside in a specially constructed pool. Although he has been labeled the “world’s fattest kid,” he proves that hard work and setting goals always pay off. Let’s learn more about Arya’s story.
The boy was dubbed “the world’s fattest child.”
Arya Permana is 15 years old and used to eat 5 meals daily, including rice, fish, meat, vegetable soup, and a traditional soy patty. It was enough food to serve 2 adult people, on average. The little kid had to stop attending school since he’d quickly run out of breath while walking. Because his parents could no longer find clothes that fit him, Arya had been wearing nothing more than a sarong for a long time.
But eventually, he decided to make a change.
Arya Permana changed into a much slimmer version of himself from a boy weighing 421 lb (191 kg). The Indonesian student has lost a significant amount of weight at just 183 lb (83 kg), and he’s even been motivating others to adopt healthier lifestyles. Ade Rai, his trainer, assisted him in learning about physical activity and a balanced diet.
Arya is now a symbol of hope.
His trainer said that Arya initially weighed 187 lb (85 kg) before his appetite drastically grew. Now he is slimming down without losing his spirit. Notably, among adults, this is a rare quality. He’s become a symbol of hope, and now people say things like, “Even Arya can lose weight, so why can’t I?” The kid combines a strict training schedule with a nutritious diet and medical care. Ade Somantri, Aria’s father, claimed that his son’s weight loss was made possible by medical care, a strict exercise routine, and a diet.
Arya used not to be able to stand for more than a few minutes at a time. He can now play football and other sports with his pals and walk to school after undergoing a major operation to reduce the amount he eats. And we are so happy for him!
What are your goals that you’re determined to achieve no matter what? Do you have an inspiring story you want to share? We can’t wait to hear it!
Preview photo credit AFP/EAST NEWS, Future Publishing / Future Publishing / Getty Images
“People Only Know Me as a Freak,” The Wolf Man Struggles to Find a Job Outside the Circus
Jesús Aceves has hypertrichosis, which makes his hair grow abundantly over his face and back. Because of his condition, he’s also known as The Wolf Man. But he’s tired of this alias and wants to live a normal life.
Meet Jesús Aceves, a 55-year-old man born with a condition called hypertrichosis, which means he has abnormal hair growth over his body, especially his face. Although married with kids, Jesús isn’t fully happy with his living conditions. He says he and his family suffer discrimination. In an interview, one of his kids mentioned, “People call me names, and they even tell their kids not to be my friends.”
© Chuy, El hombre lobo / Chuy, The Wolf Man / Facebook
He worked in the circus all his life, traveling through several cities. But now, he’s tired of being seen as a freak. As a consequence of years on the road, he’s been known as The Wolf Man.
Back home and not in the circus anymore, he’s facing another challenge: finding a “normal” job. He needs to support his family since his wife works in temporary jobs.
After several failed job interviews, he agreed to try something he had always avoided: shave his face. He relied on his family barber to transform him, even creating eyebrows and lashes.
The experience was difficult since the face is an extremely sensitive body area, but both he and his wife believed that simply by shaving, he would be able to find a job.
Jesús did several interviews, and it’s confident that now he’ll find somewhere to work besides the circus. If this happens, he must shave his face every 2 days.
Although rare, some conditions aren’t impossible to have. Luckily, people find a way to overcome the difficulties a rare condition brings and strive in life. Hannah Tyre, for example, was born with osteogenesis imperfecta, meaning that her bones break very easily. But her love for makeup made her an internet influencer, reaching millions of followers. We hope that, by reaching the mainstream media, people with genetic diseases won’t suffer more discrimination.
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