Who will accompany you on the journey to explore the world. In the previous section, we have talked about weird babies, and in this section, we will continue to talk about 10 abnormal babies. And the first baby will be the one that will surprise everyone. Let’s come with me
10. Shiloh Pepin
Shiloh Jade Pepin was born in 1999 in the United States. Right from birth, Shiloh had a rare disease called ‘mermaid syndrome’. Shiloh’s legs stick together, and she also has some defects in the body, such as the bladder, uterus, rectum, vagina with only 1/4 kidney, and one-sided ovary. At the age of 3 months, Shiloh’s kidneys stopped working, causing her to live through the day of dialysis.
Over the next few years, she underwent many surgeries and lived with medicine. Most babies with mermaid syndrome cannot live longer than 72 hours after birth. But Shiloh is one of only three people in the world who continues to live for many years without surgery to separate the legs. She wrote a wonderful story about her own life.
Her parents always love and encourage her. Mr. Elmer once encouraged his daughter that it is our differences that make the world special… God makes everyone different, and each of us is special in our own way.
On social networks, many people have praised Shiloh. She has participated in many talk shows which are really sympathetic. But Shiloh died in October 2009, when she had just turned to 10. Oh my god ☹ it’s a pity! And now is the most interesting part of the, which is Ask and Answer.
9. Marcia and Millie Biggs
Marcia and Millie Biggs were born in England. They are twin sisters but Marcia inherited her mother’s appearance with blue eyes, blonde hair, and white skin, while Millie’s appearance resembles a Jamaican father with dark hair and dark skin.
This makes many people do not believe they are twins. From the young age to adulthood, the two sisters always attract attention and curiosity from others when traveling. When Marcia and Millie were in Osborne Kindergarten, the teachers had a hard time believing they were siblings.
The mother of the two girls said: “Like many twins, her children are no different. But after only a few months, changes began to take place. Millie’s skin suddenly became darker. We thought it would happen to Marcia but not at all.” Despite their differences in skin color, their faces are almost identical. “My children are all very beautiful and I take pride in it every day”
8. Tiyo Satrio Poor
Tiyo Satrio is an Indonesian. Right from birth, he did not have 2 arms, 2 legs like other normal children. When pregnant, Mrs. MiMi did not know that her child encountered this malformation. When he was born, she was really shocked about her son.
Every day, Tiyo Satrio is brought to school by her mother. He excelled in math and activities related to religion research. His mother also said that she always follows Tiyo everywhere, if she goes to work, she will not be able to take care of her child. Many will ask, how does he write? The answer is that he can write with his mouth and play games with his chin. Oh my god!
7. Vincent oketch
10-year-old Vincent Oketch lives in the Republic of Uganda for years, wearing girl dresses because his huge legs cannot fit in any kind of pants. At the moment, doctors in the village are calling for help from international health organizations because his situation is increasingly dangerous if still not intervened by advanced medicine.
At birth, he was completely normal until he was 18 months old, these abnormalities were discovered. But because the family was too poor to take him to the hospital for treatment. Until the legs became more and more swollen, the doctors here were confused and could not diagnose exactly what the problem was.
For many years, Vincent’s life has been almost on the bed and all activities such as travel, personal hygiene are almost impossible. And the boy is faced with having to cut off his legs to stay alive. A charitable organization of England has come out to call for charity for the boy. And let’s all wish that he will soon return to normal life!
6. Ollie Trezise
Ollie Trezise, a 21-month-old boy in Wales, England suffers from a rare brain hernia. Because a part of the brain overflows through a crack between the skull and the nose, the boy’s nose grows like Pinocchio in the popular cartoon.
After going through many painful surgeries to close the crack in the skull, the young Ollie was able to play normally like other children. However, many people discriminated against the boy because of his different appearance, which made Amy Poole, Ollie’s mother extremely sad. But the maternal love made her love her child even more.
It is known that during the 20th week of pregnancy, Amy was informed by the doctors about a strange soft tissue developing on the baby’s face but she still decided to give birth to him. Until February/2014 at birth, she was shocked to see her son for the first time.
In November 2014, Ollie had to undergo a 2-hour surgery at Birmingham Children’s Hospital to remove excess brain fluid and the nose orthopedic surgery was successful. But in the future, the boy still has to undergo many more surgeries.
For the boy’s mother, Ollie is the perfect child. She considers her son a real-life Pinocchio and is very proud of him. It is true that nothing more than the love of parents for their children, right?
5. Jaxon Buell
Jaxon Emmett Buell, a young boy from the US, was born on August 27, 2014, but suffered from a brain defect called Microhydranencephaly, which caused the skull to be half the size of a normal baby. Most people were surprised, and even the doctors could not imagine the miracle that Jaxon had done.
During the pregnancy, the doctors let his parents know about the condition. They were shocked, deeply thought, and then decided to give birth. The boy was born by surgery and weighs 1.8kg.
When Jaxon was just 1 year old, his parents created the Jaxon Strong Fanpage, which attracted nearly 180,000 likes. Also, Jaxon’s fund to support the situation also increased to 41,800 Pounds. And lots of foundations have helped with the hope of a better life for him.
His story has been spread all over the world media, becoming the focus of discussion for everyone. There are those who admire the strong will of the unfortunate boy. He has to be completely brave to live and until 10/2015 he spoke for the first time, making the whole family absolutely happy.
4. Jagannath
The boy named Jagannath suffered from a rare skin genetic disease called Lamellar ichthyosis. This disease causes the skin to abnormally grow, dry, and peel off like reptiles. In Jagannath’s case, the illness was so severe that the boy changed his skin every 4-6 weeks.
He had to take a shower every hour and apply moisturizing cream every 3 hours to try to ease the symptoms. Here are some shocking images of the young boy, which showed his dry and scaly skin all over his body like fish scales.
Jagannath’s skin is also so tight that he can’t walk normally, and needs a stick to help him stretch the limbs. Unfortunately, there is no cure for Jagannath’s disease. Hopefully, in the future, the charities will help him so that he can live well.
3. Maddison Gill
Maddison Gill, a 2-year-old girl from Somerset, England, has been unable to cry since her birth. At birth, babies can only squeal instead of crying like all normal children. Maddison could not even suck, swallow, and cough.
Therefore, the baby’s food and medicine must be done regularly through a tube that is constantly monitored. Doctors think that this is probably the only patient in the world suffering from this disease.
The 21-year-old Maddison’s mother always has to implement a strict care program right in her bedroom. In addition to not being able to cry, swallow, or cough, Maddison is as normal as any other child. She was able to stand on two legs and has begun to walk the first steps.
2. Charlotte Garside
Born in Withernsea, England, at birth, Charlotte weighed less than 1 kg with a height of 25 cm. Diagnosed with Primordial Dwarfism, at the age of 5, our little girl weighs only 4 kg and is 68cm tall, only a little bit more than a newborn baby.
This congenital dwarfism will appear in young children if both parents carry the gene. She was very disadvantaged and laughed at by her friends whenever they saw her. However, she still lives in love and happiness.
1. Bayezid Hossain
Living in southern Bangladesh, 5-year-old Bayezid Hossain was unable to go to school just because other children were terrified of his appearance. Progeria, a rare disease, makes the boy’s body as old as an adult, but the brain is still of a child.
While his intellect is above average, the sagging skin and other abnormalities in the body due to the disease make him look like an 80-year-old man. The boy’s parents had to go to lots of medical clinics all over the country, from doctors to traditional healers, but the boy was diagnosed that he might not survive the age of 15. Let’s all wish that he could overcome the fate.
