RoyalBlak007's Posts
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ifyan: ![]() ![]() |
Nice [color=#F5A215] Script[/color] |
olihilistic: So many options [color=#F5A215]( or over 2.5)- (x2& -(2 or )- (First HalfUnder 1.5 sef) [/color] |
[color=#1161C3]Chelsea-2 [/color] [color=#B90050]Barcelona-2[/color] |
This girl go sabi [color=#F5A215] cross ball pass David Beckham o na joke oh! ![]() |
ladycomfort: ![]() |
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Sirgay:Now I think I understand why you find it so hard. [color=#F5A215]Enjoy yourself. ..... as usual [/color] |
Sirgay:Why do you find it hard [color=#F5A215] to respect people's opinion. It's the easiest task ever[/color] |
[color=#F5A215] [/color] |
ლლლლლ [color=#F5A215] [/color] |
Something [color=#F5A215]isn't right ![]() [/color] |
BeeBeeOoh:One could rest on the smoothly smooth pole [color=#F5A215]all night long. Feeling comfy Pole [/color] |
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How I wish ßilßao could stun Åtlętico at the Calderon ![]() [color=#F5A215] ßut...but...[/color] |
Only if you're a [color=#F5A215]Weak Man[/color] |
Truth be told [color=#F5A215] NIGERIANS ♡ SĘX ALOT [/color] |
They weren't having sex [color=#F5A215]He was only humping [/color]
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kimbraa: ![]() |
Johncris Carl Quirante 300 Teeth In Cebu, Johncris Carl Quirante was born with a rare condition known as multiple hyperdontia which gives him more teeth than the average person. As his family was unable to afford a dentist until he was in the fourth grade, his mother didn’t know about his condition. However, she did notice extra teeth pushing through his gums. So she saved the money for a trip to the dentist. There, they discovered that Johncris had around 300 teeth. That is almost 10 times the number of teeth in an average adult mouth! Since the discovery, Johncris has been undergoing operations to have the extra teeth removed from his mouth. Otherwise, they could cause severe gum disease and eating discomfort as he gets older. It will take eight operations to remove all his extra teeth. These procedures will be spread over a few years to allow the gums to properly heal between each group of extractions. So far, he has not had any setbacks associated with his condition. He is excelling at school and on the playground. He remains happy and positive despite his upcoming operations. Fortunately, his condition was caught before it affected his quality of life.
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Ben Underwood Echolocation Bats are born with the instinct to use a system known as echolocation. They make noise and wait for it to reverberate off the objects around them so they know where such objects are. This brings us to Ben Underwood, who was just three years old when he was diagnosed with retinal cancer . To prevent the cancer from spreading to the rest of his body, both of his eyes were removed and replaced with prosthetics. This rendered him completely blind. Ben grew up in California with his family and lived an almost completely normal life. He had taught himself to use echolocation by creating a sharp clicking sound with his tongue. The sound echoed off nearby objects. Due to his trained ears and his insane ability to accurately determine where things were around him, he successfully lived a blind life with no guide dog and no cane. Even more incredible, he could play basketball, skateboard, and even ride a bike home from school. Unfortunately, Ben died in 2009 from the same type of cancer that had taken his eyesight. When the cancer came back, it spread to his spinal cord and brain. Ben was just 16 years old when he passed away.
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Richard Sandrak Little Hercules (AKA The World’s Strongest Boy) In 1992, Richard Sandrak was born in a small town in Ukraine . Two years later, he migrated with his parents to Pennsylvania in search of a better life. Both his parents trained with weights, and his dad was into martial arts. At age three, Richard began training with small weights to slowly strengthen his body. This all seems good and normal. However, in 1999, the family moved to California and the media recognized Richard, then seven, as “The World’s Strongest Boy.” From there, he only got stronger as he continued to build his eight-pack abdomen and his abnormally muscled body. He headlined in many famous bodybuilding shows such as Mr. USA, The Emerald Cup, Mr. Olympia, and the Arnold Classic. Critics were worried about the way in which Richard had become a young bodybuilder. Were steroids or child abuse involved? Richard never attended a normal school, and his father had been imprisoned for domestic abuse toward his mother. Reportedly, Richard had only 1 percent body fat, which is a particular health risk for a child who is still growing. However, Richard has always denied that his parents played any forceful part in his training and claims to have simply fallen in love with it when he started. In 2005, he released a video program to inspire other kids to be fit and healthy |
Kristina Pimenova The World’s Most Beautiful Girl Kristina Pimenova has been modeling since she was three years old. By age nine, she had been internationally dubbed the “most beautiful girl in the world.” Born in Russia, she began her modeling career as a toddler who was featured in campaigns for elite brands like Dolce & Gabbana and Roberto Cavalli. Her Facebook page, managed by her mother, now has over two million likes. However, critics have begun questioning the girl’s fame due to the number of inappropriate and sometimes pedophilic comments left on her photos. Kristina got into the industry through her mother, Glikeriya Shirokova, a former model who wanted her only daughter to follow in her footsteps and have the life she had. Glikeriya got the idea from taking her baby daughter to shoots where people would tell Glikeriya how beautiful Kristina was and that Glikeriya should get Kristina into modeling. From this was born the world’s most beautiful girl. While many children are in the modeling industry at young ages, Kristina stands out because she is modeling at the level of an adult at only 12 years old.
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Chinese ‘Fish Boy’ A boy was nicknamed the Chinese “Fish Boy” after he was born with a skin condition which left him covered from head to toe in scales. Unfortunately, it is an incurable condition which limits his quality of life due to constant itchiness and limited mobility. He gets relief from cold water and several medicinal creams recommended by doctors. The scales were flat when Pan was born. Over time, they developed into thick scales which prevented him from sweating. Therefore, they affect his body’s ability to cool down. Known as ichthyosis, this rare skin disease is inherited by a child when both parents pass on the same gene that causes the disorder. Over 16,000 children are born with this condition each year. Unfortunately for Pan, it is currently incurable despite the desperate efforts of doctors who have reviewed his case. His nickname is derived from the Greek translation of ichthy, which is a root word for “fish.” Hopefully for Pan’s sake, a cure will be found which will enable him to live a life without pain and illness.
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Tessa Evans Tessa Evans from Maghera was born with congenital arhinia. This is an extremely rare condition in which the infant has no sense of smell and no sinus cavities. Her parents agreed to let her be the first patient to undergo a new procedure to help her. A 3-D printer built an implant which could be placed under the skin to give Tessa the appearance of a nose. Once she has stopped growing, a tattoo artist will be able to impress natural contours and nostrils into the skin which will give Tessa the appearance of a “normal” adult. The initial surgery was a success. The implant has given her a small nasal bump which has raised the area between her eyes. Doctors plan to repeat this surgery every two years until they are satisfied that her face is no longer growing and developing. At birth, Tessa had to be tube-fed due to a tracheostomy tube in her neck to help her breathe. Aside from the first few months when she had to learn to breathe through her mouth, doctors say that there shouldn’t be any long-term internal dangers. However, her parents are concerned about the loss of natural instincts that come with a sense of smell, including the ability to detect rotting food, poison, and burning. Tessa will have to learn to rely on her other senses, such as touch and hearing, to make up for this loss.
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Shiloh Pepin Real-Life Mermaid Shiloh Pepin was born with “mermaid syndrome,” medically known as sirenomelia. Infants with this condition are born with their legs fused together. For Shiloh, doctors gave their heartbreaking prediction that she would not survive longer than a few days after her birth in 1999. Unlike most children born with mermaid syndrome, Shiloh’s legs could not be separated due to the way her major arteries were running through her legs. The condition meant that Shiloh had no uterus, bladder, or large intestine and was only graced with one partially working kidney. Despite the circumstances, Shiloh continued to prove doctors wrong as she overcame her difficulties. In 2009, she celebrated her 10th birthday. Previously, she had undergone two kidney transplants and a number of other operations to prolong her life. She proved to the world that she was born a true fighter. She attended school, appeared on several talk shows, including The Oprah Winfrey Show , and was an inspiration to children all over the world. Unfortunately, her fight came to an untimely end at age 10 after a cold quickly turned into pneumonia. Her body was unable to fight it off. Shiloh Pepin’s story will continue to inspire children with disabilities all over the world. She was the girl who never took no for an answer, and it showed in her relationships at school and in her personality.
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-(2 or )- (First HalfUnder 1.5 sef) 


