Pony’s real name is Kim Hye Min, known in the industry as a blogger, makeup artist for singer CL. Her beauty-related channel currently has over 5.8 million subscribers from around the world. Pony’s most viewed video featured her transform into Taylor Swift in 2016. Difficult first days “In the beginning, it was just a diary. I introduced different trends as well as skin care and beauty. Those are my personal feelings and thoughts. However, when the channel and The number of viewers is growing, I have to know how to moderate,” Pony said. Pony once surprised many people around the world with makeup identical to Taylor Swift. Photo: Daily Mail, Pony. Pony considers herself a “first generation” vlogger in South Korea, where social media platforms have fueled the careers of many influencers over the past few years. When Pony started working on it, things weren’t completely standardized and she had to spend a lot of time being creative. She considered herself how to present her content in new mediums after spending so much time blogging. At that time, Pony’s decision was seen as a great challenge, as meaningful as a pave. She sees it as a journey to learn. The most difficult thing for a female beauty blogger is to do everything by herself, even paying attention to each punctuation mark. Kimchi makeup expert confided: “It is certainly not the easiest path. However, it is an interesting path, paving the way for those who have influence on beauty. You have to be careful even when using a basic emoji. It may be wrong in some people’s opinion. Because someone goes first, the juniors will feel less difficult.” Promoting the Korean beauty industry According to the SCMP , Pony has been instrumental in the fact that Korean products can be found in most beauty and convenience stores worldwide. Pony is now very influential in promoting the Korean beauty industry. Photo: @ponysmakeup. She said, “As a Korean, it’s surprising to me that so many people know about K-beauty around the world. But on the other hand, it’s a mixture of disappointment and optimism.” Pony thinks so because she thinks she and others have the opportunity to continue to spread news, views about Korean culture, beauty products. However, the industry has stalled. When thinking about kimchi beauty products, many people immediately know foundation, sheet masks, multi-step processes, snail cream, etc. According to Pony, these basics are still relatively new to the audience. She wanted to show people more of those things. From there, the 31-year-old makeup artist hopes to revive the industry once again through sharing her different skin care and beauty regimens with the world. In addition to beauty, Pony’s style of dress also becomes an inspiration for girls. Photo: @ponysmakeup. “In Korea there are only 2 types of foundation. In the US, it is available in different levels. Because of the lack of color variety, our products are distinguished through different finishes such as glass leather. , frosting, airbrush, velvet… with skin-supporting ingredients,” emphasized Pony. After researching, she wanted to combine the two things together so that more people around the world could “enjoy” a variety of foundations. Although Pony’s work has changed slightly due to the Covid-19 epidemic, she continues to pursue international projects as a brand ambassador, creator or event organizer. “I want to make everything accessible to everyone,” she is adamant.

Every nearly 4:30 pm, Mr. Phuoc pushes his bread cart to the markets and garment companies near his home to prepare to welcome the first guests. Bread of all kinds of shapes of Mr. Phuoc attracts the curiosity of the people around. Thanks to a predestined business relationship, he was bought by many young people for support, and from 7pm he was out of bread. The 37-year-old boss said that he has been in the business for about 20 years, but has only been engaged with animal bread for 6 years. Improving, accumulating many years as a hired man, Mr. Phuoc has opened a small bakery for about 2 years. Mr. Phuoc has worked as a bread maker for about 20 years. The difficulty of making animal bread Taking advantage of the space in front of the ground floor, Mr. Phuoc opened a small bakery. There are no eye-catching advertising signs, inside only an oven and a few baking tools. As a small business, everything from preparation to sales is done by him. After mixing, the owner rolls the dough into even pieces to shape. From the fine round dough, Mr. Phuoc skillfully molded it into many different shapes. “The shaping stage is the longest. At this time, the worker needs to be patient, careful, with many details, it is difficult to invest time in practice. Usually, I squeeze a baby about 7-8 minutes, ”the 37-year-old owner chatted with reporters while meticulously adjusting the cake. Beautiful bread rolls are baked after many different stages. Mr. Phuoc can shape more than 10 animal models such as dragons, spiders, turtles, crabs … However, he only chooses his favorite models for sale. Each one has its own unique features, but the best-selling models are still crocodiles and horses. These are also the two most difficult pictures to do because they have to cut and graft the dough, it takes more effort. When forming, the dough is incubated for one more hour. It takes almost 2 hours from the first step to the finished product and then 15 minutes of baking on high heat. “With baking, baking time is the most thrilling. Because I thought it was beautiful when I did it, but it didn’t look like I wanted it, it took time to correct it, ”added Mr. Phuoc. With animal-shaped bread, the cake will have a soft intestine when it is finished, but other parts such as the legs and beard are always more crispy or easy to be hard if baked over heat. Strange animal-shaped bread Mr. Phuoc’s baking job started from late evening to early morning in order to make it in time to sell. In the morning, Mr. Phuoc made about 1,500 small loaves of bread. Around 2-3 pm, he continued to bake big cakes, priced from 25,000-70,000 VND depending on the model. “My regular customers are mostly workers and students, so I only sell them at affordable prices for everyone to buy. They also love my bread, they buy it every afternoon. Someone bought them as gifts for their children and grandchildren ”, confided the baker’s owner. Mr. Phuoc often sells in areas near his home. Animal-shaped sandwiches received a lot of attention when he joined the show Challenging comedians season 3 (2016). In his skit, Mr. Phuoc impressed two judges Truong Giang and Tran Thanh with the charming and friendly style of selling bread. “That was the first time I brought animal bread on stage. After the show, my bread was known by many people. One day there were people selling them to the market, they asked for a photo together. Although there are no awards at all, it is also the most memorable memory since entering the profession “, Mr. Phuoc shared. His bread is loved by both children and adults. Minh Thu (23 years old, Binh Tan district) often stops to buy bread from Mr. Phuoc on his way home from work. Two of Thu’s most favorite patterns are the crocodile and the turtle image. Thu said that the intestine of the cake was already soft and fragrant, so just dipping it with a little condensed milk was delicious. “Every afternoon I see the owner selling here. Sometimes when we come out late, we run out of cake. People buy a lot, especially around 5am, ”said Thu. Although not a bread fan, every time I visit, Huynh Trang (25 years old, Binh Tan district) still buys at least 5 loaves because he likes the strange and unique shape. “I bought it for a long time. Every time I came over, I saw Mr. Phuoc making more new ones such as spiders, snakes, crickets… I often bought them for my younger siblings at home to eat together. It was strange, so the kids enjoyed it, ”Trang said.

Virsaviya Borun. Born with rare syndrome In 2017, a 40-second video showing a dramatic scene of a girl’s heart pounding out of her chest caught the attention of many people. The little girl in that amazing video is said to be Virsaviya Borun, from Russia. Despite living with such a disability, Virsaviya loves life very much. In a clip on YouTube, Virsaviya surprised everyone when chatting innocently, making a playful gesture with the heart outside his chest, making many listeners shed tears. Virsaviya is also regularly posted by her mother on Instagram, the latest picture shows the mother and the child in swimsuits. “I like to paint Jesus, foal and angels. I don’t go to school and don’t ballet, but at home I still study and dance. This is the heart, you are the only one with it. When wearing clothes, children undergarment soft so that the heart does not hurt. You go, run, jump. I shouldn’t be able to run, but I like to run, ”she said. Born in 2011, the baby girl Virsaviya Borun suffers from a syndrome of “lost heart” also known as the Pantalogy of Cantrell. This syndrome prevented her ribs and abdominal muscles from being properly formed during her pregnancy. The Pentalogy of Cantrell has varying degrees of severity. Some newborns may have only mild malformations, some more severe can have life-threatening complications.In those cases, the extrasoracic heart is the most common form and are also the most dangerous, accounting for 59% of all heart defects. In practical terms, the only two types of heart that are out of place of clinical significance are the extrasoracic heart and the heart outside the chest-abdomen area. Virsaviya Borun has a rare syndrome called the Pentalogy of Cantrell, meaning “lost heart”. Virsaviya Borun is one of these unlucky ones, because her heart is completely exposed on the outside of her chest and only protected by a very thin skin layer. While it doesn’t cause too much physical pain, it will make her heart appear exposed as it is just below the surface of the skin. According to the doctors, not only the baby’s heart lies outside the chest, but her intestines are also protruding out. The exact cause of the Pentalogy of Cantrell syndrome is currently unknown. Almost all cases are random, for no apparent reason. It is hypothesized that symptoms of the Pentalogy of Cantrell are due to abnormalities in embryonic tissue development during pregnancy. Her phenomenon is extremely rare, only happens with a rate of 1 person per 5.5 million people. According to statistics, only 50 cases of the same disease are known to survive by the age of 12 in the world, the rest of which die a few hours after birth. Virsaviya Borun is with her mother and younger brother. Always love life, not surrender to fate While Virsaviya’s mother Dari was pregnant, she was told that the little daughter in her womb could die during pregnancy or birth. However, despite the difficulties, Virsaviya still lives healthy. “The doctors told me that my daughter could die while I was pregnant or during childbirth. But with what’s going on, I can only say that, Virsaviya is truly a miracle and I love Virsaviya. Virsaviya is unique to me. One of the millions of most special people in the world, ”said Ms. Dari. Her heart is about the size of a hand, always on the outside of her chest. Virsaviya’s family always hoped that she had a body and a normal life like everyone else, so Virsaviya needed several complicated surgeries. Because the cold weather would endanger my health, they moved me to Florida (USA) to live and continue to treat. Currently, I live in Hollywood, 32km from Miami, Florida and quite healthy. Accordingly, in 2015, with the hope of helping Virsaviya to have a normal life like many others, the mother and daughter recently arrived in Boston, but the Boston Children’s Hospital could not operate on Virsaviya because of her aortic blood pressure. baby is too tall. So far Borun’s family has taken their daughter to Hollywood, in the hope that the treatment will lower her blood pressure enough to undergo surgery. After that, Virsaviya’s condition caused her to be hospitalized for a long time. They even said that families should prepare themselves mentally for the worst situation. Having undergone many painful surgeries but Virsaviya Borun is always optimistic and loves life. Borun’s family went to the best pediatric hospitals everywhere. Several hospitals around the world have had to relocate Dari’s daughter to another because of the difficulties and risks that can be encountered if surgery is performed. In early 2020, blood oxygen levels suddenly dropped, causing Virsaviya to experience dizziness and difficulty breathing. Virsaviya was immediately taken to the emergency room and monitored by doctors to ensure complete stabilization of the oxygen intake. Since Virsaviya was born, the doctors told her mother Dari Borun that she would not live long. However, 11 years later, I still live healthy and extremely active, active, like to draw horses and take art classes like normal people. Besides, I also love to run and take dance lessons but Virsaviya’s current state does not allow me to do that. Virsaviya’s mother shared: “It is not easy for Virsaviya to live with such an outside heart because it is too fragile. She can die just from a fall. Virsaviya’s little brother – Ervin is also very fond of approaching and touching his sister’s heart. “Ervin always thought Virsaviya’s heart was something wonderful and beautiful. Ervin especially likes to lie on Virsaviya to feel the pulse of his heart and see the full miracle, ”Dari said. Although Virsaviya knew her situation could take many risks, the little girl never surrendered to fate. “Sometimes I can have some difficulty when the oxygen level in the blood drops, making me dizzy and my health is seriously affected. But I will always try to be able to maintain my life and sing and dance activities with my friends. I really like this. 2020 could be a very boring year for the whole world because of Covid-19’s influence, we were unable to go anywhere or do anything, but I chose to spend more time with my brother and my family. I realize that is really great. Not only that, but I also receive a lot of messages from people who love me on Instagram. They said that I am a strong inspiration, so even though my heart is different, it makes me special and I love it, ”said Virsaviya. The touching story of Virsaviya was first known in 2015 and has spread around the world, shocking everyone about the little girl’s extraordinary vitality. Although her body is not normal, this courageous girl is still very optimistic and loves life. I never thought I was sick but believed that, because God wanted to prove He could do special things, so created me. In the past, Virsaviya’s mother opened a fund to fund her surgery and received about $ 71,000.