A woman who tattooed her boyfriend’s name on her forehead is defending her face art, suggesting that anyone who refuses to do the same, isn’t really in love.
Ana Stanskovsky, who penned a permanent love letter to Kevin on her face, insists it’s an expression of love, but online users are saying “it’s stupid” and that her “next boyfriend will hate it.”
Polish-born Ana Stanskovsky surprised her 588,000 TikTok followers by sharing a post of her newly transformed face.
In a viral TikTok clip, Stanskovsky is seen sitting in a chair, having some work done to her forehead.
The “my new face tattoo” video, which has 18.3 million views since it was first shared November 6, shows Stanskovsky getting her boyfriend’s name, penned in large black cursive letters, across her forehead.
The clip zooms in on the artist permanently inking over the stencil that reads “Kevin,” and Stanskovsky wincing in pain.
When the art is complete, she stands up to view her extreme expressions of love in the mirror
“Done? Okay let’s see. Oh my God, I love it. Wow, Kevin’s gonna love it,” she says.
She finished the clip by asking her followers “Do you think he will like it?”
Responding to her question, one netizen jokes, “He’ll love it! Your next boyfriend will hate it though.” Another user writes, “I don’t know who Kevin is, but wherever you are…. Run!”
As the video hits the eyes of the puzzled social community, people are warning her of future regrets.
“Great decision here. I don’t see how you could ever regret this,” one fan shares.
Replying to the overwhelming suggestions of regret, Stanskovsky fired back with another clip saying she will never regret the Kevin tattoo.
Stanskvosky replies, “I know many of you said I’m gonna regret that and what if we break up and all of this stuff, all of this horrible stuff and I just wanna say this is how I’m expressing my feelings so if I love someone, I’m doing this.” She continues, “I’m loving it, I’m definitely never gonna regret that. How can I regret this? It’s beautiful.”
“A handwritten note is a precious way to express your feelings,” quips one cyber citizen.
Fans still aren’t convinced, and many think her outrageous announcement of love must be a joke.
“Wait. Wasn’t it a joke?” writes one while another says, “I was waiting for them to say it’s just a prank but they never did.”
The influencer then tells viewers that every time she looks in the mirror she is “in love.”
“I’m in love with the tattoo and I’m in love with my boyfriend,” she said. “I think if you really love someone, you’ve just got to show it you know, you’ve just got to prove it…So I think if your girlfriend doesn’t want to tattoo your name on her face, you just need to find yourself a new girlfriend because I don’t think she loves you.”
Shocked by her comment, users jumped in saying she needs to reconsider her shows of love.
“‘if [your] girlfriend doesn’t want your name on the forehead she doesn’t love you,’” One netizen writes, quoting her. Then offering this advice to Kevin, the user continues, “dump her ASAP.”
Given the uncertainty of relationships, one netizen asks, “and if he breaks up with you what then?”
Stanskovsky answers: “What if we break up? I’ll just have to find myself a different Kevin.”
But one person has a better idea: “It would be better if you wrote on it that I am stupid.”
At the moment there’s been no response from Kevin.
What do you think of this woman getting her boyfriend’s name tattooed across her forehead?
There are far better ways of expressing your love, and if you insist on a grand gesture, maybe a smaller tattoo in a place it’s not so visible?
Mom of Boy with Rare Condition Shares Their Life, People React Differently
Logan Pacl stands out among teenagers. At 17, he faces a rare illness known as Sanfilippo syndrome. Often called “childhood Alzheimer’s,” this cruel disorder gradually takes away a child’s cognitive skills, mirroring the effects of Alzheimer’s in older people. But he keeps fighting and uses social media to spread awareness about his condition.
At first, everything seemed normal.
Logan Pacl’s life is a battle against time. Diagnosed with Sanfilippo syndrome, often known as “childhood Alzheimer’s,” the 17-year-old from Silverdale faces a relentless genetic disorder that viciously strips away the very essence of childhood. Caused by a single defective gene, this neurodegenerative disease attacks the brain and spinal cord, leaving behind a cruel wake of lost abilities, seizures, and constant pain. It’s a ticking time bomb, as most children with this terminal illness don’t survive beyond their mid-teens.
For Logan’s family, the heartbreak began early. Born in 2007 with his twin brother Austin, Logan seemed like any other healthy baby. Both boys hit their developmental milestones—until Logan began to fall behind. A year in, the red flags emerged: while Austin was speaking, Logan remained silent. The difference between the brothers grew, signaling the start of a devastating journey.
Sanfilippo syndrome doesn’t just rob children of their future—it erases their past.
Then the news of the diagnosis hit the parents, something no one could have anticipated.
As Logan’s condition worsened, with chronic infections and a noticeably swollen belly, Noelle and William were left searching for answers. In January 2010, they learned that Logan had Sanfilippo syndrome, a terminal illness with no cure or treatment, and a life expectancy that typically extends only into the late teens. “I’ll never forget the day we got the phone call. The genetic counselor on the other end went on and on, and all I thought was, well get to the part on how we fix this. Then she said it, ’This disease is terminal, and there is no cure or treatment,’” his parents recall.
Noelle recalled her initial reaction, grappling with the news that the disease was terminal. The weight of the diagnosis was overwhelming, leaving her with a heart that felt as though it had dropped into her stomach. The severity of the situation rendered her unable to process much beyond the devastating reality.
Noelle described the experience of mourning not just the child she had but the life she had envisioned for him, a life that was abruptly stolen away. The medical advice they received was minimal and unhelpful, simply advising them to take Logan home and cherish their time with him. This lack of concrete guidance only deepened their sense of helplessness.
In their search for hope, Noelle and William discovered an experimental stem cell transplant through online research. Inspired by the success of another mother’s child, they decided to pursue the same treatment for Logan. So, Pacl went through a tough three-month treatment that was basically a bone marrow transplant. He had to endure chemotherapy to wipe out his immune system so it could accept the new stem cells. It was a risky procedure, but it seems to have helped with some of Logan’s physical symptoms.
His mother uses social media to spread awareness about his condition.
At 17, Logan’s life is very different from that of most teenagers. Losing his ability to speak at a young age was tough for him and his family, but over time, he’s become more easygoing. “Life with Logan is anything but typical. Each day is a battle to maintain the skills he still has,” his mother Noelle said.
Since 2020, Noelle has been a vocal advocate for Sanfilippo syndrome, using TikTok to share her family’s story. Her videos have reached a global audience, raising awareness about the disorder and encouraging other parents to seek early diagnosis for their children.
Although Logan’s future is uncertain, the Pacl family is committed to making the most of their time together. Noelle and William used to avoid thinking about what lies ahead, but now they focus on cherishing every moment with Logan and ensuring he enjoys his time to the fullest. Noelle notes that among Sanfilippo parents, there’s a bit of a joke that all their children seem like siblings, sharing similar features like bushy eyebrows, a low nasal bridge, and large, round stomachs.
Even with the demands of caring for Logan, Noelle keeps life as normal as possible for Logan’s siblings, Austin and Aidyn. She acknowledges that having a brother with special needs can bring its own set of benefits.
As for sharing Logan’s journey online, Noelle remains thoughtful about what she posts. While she plans to continue sharing, she’s careful to respect her family’s privacy. “We just live in the moment,” his mother said. “And if something comes up, and we’re like, we can make that, we’ll do it.”
People in comments react differently.
Mostly people express support and empathy.
- You take the most wonderful care of him. You are the greatest mom. © lauralang1108 / Instagram
But some show a bit of skepticism.
- Genuine question, what is your plan when you are gone? © devin_abq.505 / Instagram
- I just wanna know why it’s necessary. People have to publicize their children’s conditions. Why do people think that we all wanna know what’s wrong with your child? I feel sorry for the parents, but I don’t know why you want to put this all out there. I’m sure you have support group publicizing putting your child out there like this. © marlawomble / Instagram
Today, conversations about living with disabilities are becoming more open, especially on social media. Celebrities are sharing their experiences as parents of children with special needs, helping to normalize these discussions and inspire others. This shift fosters understanding and empathy, creating a more inclusive environment for everyone.
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