A Girl Is Called “Hulk” Due To Her Rare Condition, But She Has the Perfect Response to All the Trolls

Olivia Klopchin was born with a rare vascular malformation that caused her arm to swell and discolor. What began as a small bruise at birth soon became a lifelong condition — and a powerful platform for self-love.

Now 19, Olivia shares her journey on TikTok, where she’s earned both admiration and unwanted attention. While many praise her confidence and beauty, others have left cruel comments, even comparing her to the Hulk.

Still, Olivia doesn’t let it get to her. “I knew from a young age that people would stare — and that was okay,” she says. With humor and honesty, she responds to trolls, often turning negativity into teachable moments. “There’s always going to be negative people online. That’s something we can’t escape.”

Her openness has inspired many, including parents of kids with similar conditions. One follower wrote, “Your videos have given us hope for our son’s future.”

Olivia’s mom says she’s always stood strong: “It’s her normal, even if it’s not everybody else’s.” And Olivia agrees. “My arm hasn’t held me back. I still played sports, made friends, and answered questions without shame. I could focus on the pain — but I choose not to.”

Her story is a reminder that confidence can silence cruelty — and that kindness matters more than ever.

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