Caden Benjamin already weighed 90 kilos at the time he was 10 since he suffered from the rare Prader-Willi syndrome,…
Caden Benjamin already weighed 90 kilos at the time he was 10 since he suffered from the rare Prader-Willi syndrome, a condition characterized by obsessive obsession. On November 15, he died at the Steve Biko Hospital, Pretoria, in South Africa’s Gauteng province, Daily Mail reports.
Because of the condition, Caden was never full because his brain could not detect that his body did not have to eat more directly after eating a full meal. Eventually, the eleven year old was eating toilet paper and dirt if he could not consume anything else. The caden had to undergo a tracheotomy several years ago because of his obesity, after which he was permanently breathed through a tube that sat in his trachea, reports said. In addition, he suffered from an expanded heart, diabetes and depression due to his condition.
After her mother, Zola could not afford Caden care, but the Gila Sacks family started a crowdfunding campaign to get money for the kid. After his death, the campaign was expanded to support his funeral expenses. According to sacks, Zola was “devastated” by “losing her only child” and said that Caden was her “whole life”.
The troubled mother had described the condition of her son last year. “At a time, Caden had a toilet paper. He would eat rolls of it,” she said. “In fact, he would eat some paper he would find in the house. If there is nothing for him to eat, he’ll scrape the dirt he finds on the floor and eat it.”
That said, thousands of people worldwide suffer from physical, mental and behavioral problems because of the incurable Prader-Willi syndrome. What’s worse is that patients need less food than their peers because their bodies have less muscle mass and tend to burn fewer calories. However, they stop eating a lot more. Zola said last year: “At three years he was 40 kg (6 pounds 4 kg) and by that time we did not know what was wrong with him. We went to a number of doctors and no one could tell us what was wrong and why He got so much weight. “
It was only later that a doctor at the Steve Biko Academic Hospital in Pretoria diagnosed Cadden’s disease after driving several tests. Benjamin continued: “Normally he would start the day by eating four slices of cheese bowl and for an hour later he would drink Coke and eat leftover food from the night before. He would eat two big pieces of chicken at lunch. He would eat an hour for the rest of the day. “
Could not find a solution for its ever increasing weight and impairment of health. Doctors provided a diet for the young Caden ̵
1; who had men XL size clothes because of their size. Zola described every day as a “match” when she had to lock all the kitchen cabinets and the fridge and hide all the food items in the house. Having been unable to live as a normal child and play with the other children, the caden was often affected by depression. Many times he would break into tears and say he would go out and play with his friends.
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