In a world with defined beauty standards, it takes courage to embrace one’s uniqueness fully. Rada, a stunning model, exemplifies this courage as she proudly defends the distinctive patch of hair that grows from her forehead against online trolls and critics.
She went viral for her unique look
At just 18 years old, model Rada Prelevic, also known as Rada Viic on Instagram and TikTok, has captured the attention of social media users worldwide due to a distinctive feature: long strands of hair that gracefully hang from her forehead. Despite the fascination for her unique trait, Rada often finds herself subjected to harsh criticism and hurtful comments online. Trolls label her appearance as «bizarre» and suggest that she remove the locks.
In a candid video shared with her followers, she courageously affirmed that she really loves her hair and she won’t shave it. She also questions herself about why her unique hair bothers so many people.
She was born with it.
The Serbian-born model, now based in Oslo, Norway, where she has been living since the age of 5, shed light on the origins of her distinctive feature. Reflecting on her unusual trait, Rada explained that she was born with it. And there’s no explanation as to why the hair is placed on her forehead and has grown so much. She only knows that the patch is a birthmark.
The hate doesn’t bother her.
Rada’s confidence in her appearance is not only admirable but also inspiring. Despite the online hate, she remains firm in her conviction that her forehead birthmark is a beautiful and integral part of her identity. Her refusal to conform to societal pressures sends a powerful message of empowerment and self-acceptance to her followers and beyond.
The amount of support from Rada’s followers serves as a reminder that kindness and acceptance far exceed negativity. Hundreds of supportive messages flooded the comments section of her post, applauding her confidence and praising her unique beauty.
Her hair helps her modeling career.
For Rada, the unique lock of hair coming from her forehead has evolved into a unique feature, one that she proudly embraces as her personal «trademark» within the fashion industry. She notices that fashion magazines and photographers love her appearance, making her even prouder of the way she looks.
In matters of love and relationships, Rada’s self-assurance extends to her personal life as well. She says that she would never compromise her authenticity for the sake of romantic companionship. She firmly states that she would never be in a relationship with someone who doesn’t appreciate her for who she is.
Rada’s resolute self-confidence and refusal to conform to societal standards of beauty serve as a powerful reminder of the importance of embracing one’s individuality. In the face of relentless criticism and online hate, she remains firm in her self-acceptance, inspiring countless others to celebrate their unique traits and differences without fear or hesitation.
Preview photo credit rada.viic / TikTok, rada.viic / Instagram
Jase and Missy Robertson’s journey: Overcoming obstacles and finding strength
Mia Robertson, the youngest daughter of Duck Dynasty’s Jase & Missy Robertson, has been born with a condition known as cleft lip and palate, a gap in the upper lip that can involve the gum as well.
The U.S. Centers for Disease Control and Prevention shares that about one in every 1,600 babies is born with a cleft lip with a cleft palate in the U.S.
Because of her condition, sweet Mia, who is now 18 years old, has been forced to undergo 13 surgeries, with the 14th taking place just recently. The family truly hopes this would be Mia’s last procedure before her problem is finally solved.
Throughout every surgery, the young girl remains positive. What’s most, she hopes she serves as inspiration for other young children who are born with the same condition. On her own initiative and with the help of her family, Mia established the Mia Moo Fund in order to assist in making certain that each and every child wears a smile on their face.
“One of the functions of the Mia Moo Fund is to spread awareness of the cleft lip and palate journey,” Missy Robertson told Christian Post. “The other one is to help with medical funds for the parents and the families living right here in America.”
On his podcast Unashamed, Jase Robertson shared an update on Mia’s condition and said that his daughter is recovering well.
“She’s doing great. She’s turned a corner,” he said, and then added, “Everything seems great, seems to be fine.”
“Surgery went a little longer than expected, but she is home and recovering,” the loving father told his podcast listeners. “Thank you for praying for her and for our family. She is a champion!”
Before the surgery took place, Missy spoke of her daughter’s condition and explained that she had been constantly asked about the number of procedures Mia would need to undergo in the future. “There is never any other response than ‘We just don’t know,’” Missy said. She then added that they rely on God for assistance. “Since she is 18 now, she is taking the lead in all the discussions and medical forms. It’s been a little strange,” Missy wrote. “But it’s just another reminder to lean on the Lord and that I’m not in control.”
Mia also hopes that she’s at “the finish line.”
“Hopefully the last time I’ll see my doctors in this setting! It’s been a long road but we are at the finish line,” brave Mia said.
The Robertson’s have also been preparing for a new addition to the family as they open the doors to their hearts and home for a child whose mother was unfit to take care of.
We wish Mia speedy recovery.
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