A girl, once labeled “wolf girl” and “monkey face” by her peers, knew that her condition wouldn’t stop her from finding happiness. Eventually, she discovered the love of her life, and her story reveals the profound impact it had on her life.
Supatra “Natty” Sasuphan, once dubbed the world’s hairiest girl, faced ridicule and fear from her classmates due to her unique appearance.
On August 5, 1999, something important happened in Supatra’s family. Usually, when a new baby is born, parents feel really happy and excited. That’s how Supatra’s mom and dad, Sompon and Samrerng, felt when she was born.
But their happiness was mixed with surprise, fear, and disbelief because the doctortold them their baby had a lot of hair. At first, they thought it was normal, but when they saw her in the incubator, they were shocked by how much hair she had. Supatra’s hair covered almost her whole body, and even the doctors in Thailand had never seen someone like her.
Later on, doctors figured out that Natty had a very rare skin disease called Ambras syndrome. This condition is so uncommon that there have only been 50 cases like hers documented in the world since a long time ago.
Ambras syndrome causes excess body hair growth, sparing only the palms, soles, and mouth interior, likely due to a sudden DNA change.
When Natty was born, and her mom wanted to leave the hospital, the doctors didn’t want to let her go because they were worried she might leave her child behind. Sompon told the doctor that she would never abandon her child, no matter what. She said, “We are lucky that she was born into our family.”
Natty grew up in a loving family, but not everyone was understanding of her condition, and she had to deal with some unkindness from strangers and peers.
As Natty grew up, her face remained hidden behind thick hair due to her incurable Ambras syndrome. Regular methods like laser removal couldn’t slow down her hair growth. At school, she faced ridicule because of her unique appearance. Kids called her names like “wolf girl” and “monkey face.”
Natty, however, didn’t understand why they teased her, as she considered herself a normal girl with just a bit more hair. She stated, “It’s the way I am.”
Natty’s teacher, Kuljira Posaeng, revealed that other kids were initially scared of Natty’s appearance, making her early school days difficult. Over time, though, Natty proved she was just like any other student. Teachers described her as hardworking with good grades, and she eventually became one of the most popular kids at school.
Natty’s teachers said she was a lively girl who loved to sing, dance, and act. Her parents treated her just like any other kid, and they never made her feel like she was less important. They took her everywhere and weren’t embarrassed that she looked different from other children.
Later on, Natty found her love.
Natty has come to terms with her condition, understanding that there’s no cure for it. She decided to keep her body hair the way it naturally grew from the time she was born, only shaving her face when she became a teenager. As she grew older, her self-esteem and self-image became more important to her, and she also found love.
She shared: “It began from friendship, then we became a couple.” Their conversations brought her happiness, and being together was comfortable, with a love she didn’t anticipate: “It was a kind of love that I didn’t expect would happen to me.”
Natty later married her boyfriend, calling him “the love of my life.”
She also posted pictures with her lover, showing her face without facial hair. Some people thought she might have been cured, but her dad explained that she had chosen to shave her facial hair to reveal her new look. Now, her eyes, face, mouth, lips, and cheeks are visible, with only her forehead covered by her head’s hair.
Natty, who has found love and happiness, is determined to lead a positive life and continue making a beautiful impact on society. She believes that everyone is beautiful and unique in their own way, and she wants to inspire others to embrace their individuality and radiate their inner beauty.
Before you go, be sure to check out another article where a woman shares her story to emphasize that body hair shouldn’t be criticized, highlighting the importance of self-acceptance and embracing one’s uniqueness.
Preview photo credit Guinness World Records / Facebook, truly / Youtube
The First Ever Albino Twins Born In Argentina Will Leave You In Awe
Virginia and Catalina are two albino girls from Argentina who became viral on social media when they were born four years ago.
In 2018 Jorge Gomez and his wife received the good news that they were going to become parents to two twin baby girls. The couple already had a son and became ecstatic when the doctors told them they were expecting twin girls.
According to Gomez, the pregnancy was completely normal, and his wife used to visit her doctor regularly.
“When they gave us the news that we would have two babies, it gave us a lot of happiness, and when they were born, and we saw that they were albinos that happiness did not change at all. For us it is a blessing,” he told a local news outlet.
The father-of-three said that there were no complications and everything went smoothly. However, in the 36th week, doctors told him that they had to deliver the babies immediately.
So, the girls were born prematurely in the 36th week. But they were healthy and weighed normal. Catalina was born two minutes earlier than Virginia. They both weighed 5.95 lbs and 5.5 lbs, respectively.
The unusual thing about the newborn girls was their milky white hair. Gomez and his wife didn’t see any kid like that before in their lives, nor did anyone else.
So, the girls became an overnight sensation in Argentina in 2018 and made headlines in many media outlets and newspapers.
The pictures of them went all over the internet, and people were amazed to see two small girls born with snow-white hair.
According to LV12, the twins were born with a rare genetic disorder, albinism in which there is a lack of pigmentation in the skin.
People with albinism do not have enough melanin pigment in their skin and are born with either white or blonde hair. This condition also affects their coloring and eyesight. Some babies even have ginger hair, depending on the amount of melanin in their skin.
Catalina and Virginia were the first-ever kids born with albinism in Argentina. Their rare condition made them popular in the country.
“When they gave us the news that we would have two babies, it gave us a lot of happiness, and when they were born, and we saw that they were albinos, that happiness did not change at all,” Jorge Gomez told LV12.
He said he felt super blessed to be their father and never once thought that they were different from other kids or something was wrong with them.
“There were some precautions that we as parents had to bear in mind. For example, the girls are extremely sensitive to UV rays, which affect their skin and can cause sunburn and even cancer in a worst-case scenario,” said Gomez.
“So, we have to be extra cautious all the time and make sure that they are not going in the sunlight and are well protected from extreme weather conditions, especially hot weather.”
The twins are now four years old and look even more beautiful as they are growing up.
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