In an age where unrealistic beauty standards and airbrushed images saturate media platforms, one mother’s bold decision has ignited a fierce debate. Instead of following what everyone else thinks, she did something empowering and accepting. She painted stretch marks on her daughter’s doll.
Kate writes books for kids.
Kate Claxton, is a talented author dedicated to inspiring children. Among her notable works is the multi-award-winning picture book, “My Mum’s a Tiger!” Crafted with love and a profound understanding of the challenges faced by many, Claxton created this heartfelt story as a cherished gift for her baby’s first birthday.
Little did she know that her creation would transcend personal boundaries and resonate with countless individuals around the globe. “My Mum’s a Tiger!” serves as a powerful reflection of the experiences of numerous real-life people who grew up being told that their scars, stripes, spots, and so-called ’flaws’ should be concealed.
She has body-inclusive dolls for her kids at home.
Claxton not only writes empowering books but also practices what she preaches in her own home. Recognizing the importance of body inclusivity and normalizing the beauty of individuality, Claxton provides her children with body-inclusive dolls. As much as she adores her acclaimed work, “My Mum’s a Tiger,” which beautifully embraces tiger stripes and other unique features, Claxton understands her daughter’s fascination with dolls and their ability to be dressed and undressed.
Consequently, she took it upon herself to modify one of these dolls, adding the very stripes that so many people cover up. Claxton believes in embracing differences and encourages others to do the same, offering a poignant line from her book: “Let’s take what makes us different and instead of trying to hide, let’s be more like animals and wear our marks with pride.”
Some people criticized her for painting the dolls.
Inevitably, not everyone embraced Kate Claxton’s initiative of painting the dolls. But Claxton takes pride in the fact that her Barbie craft session sparked conversations and stirred up reactions. However, she acknowledges that reading the comments can sometimes be disheartening, particularly when encountering individuals who completely miss the point.
Among the critical comments, one person questioned the motive behind painting the dolls, asking, “Why make young girls worry more about their bodies? I’ve got no stretch marks, so maybe it would be better to teach them about being positive rather than negative about their bodies.” Another comment echoed a similar sentiment, stating, “Why make girls worry more all the time? I had three kids and no stretch marks. Make them think positive.”
She doesn’t listen to the mean comments.
Despite encountering some less-than-supportive remarks, Claxton chooses to scroll past those comments, refusing to let them overshadow the positive impact and meaningful discussions her efforts have generated. While acknowledging these differing viewpoints, Claxton remains committed to her mission of promoting positivity and fostering a healthy body image in children.
Another mom that received a lot of attention for her unique parenting style was actress Kristen Bell. Known for her refreshing approach to raising her children, Bell brings a combination of compassion, empathy, and open-mindedness to the table. In a candid moment on her podcast, Kristen Bell openly shared a personal anecdote about her daughter’s developmental journey, revealing that her daughter wore diapers until the age of 5.
Preview photo credit reallyratherwild / Instagram
“People Only Know Me as a Freak,” The Wolf Man Struggles to Find a Job Outside the Circus
Jesús Aceves has hypertrichosis, which makes his hair grow abundantly over his face and back. Because of his condition, he’s also known as The Wolf Man. But he’s tired of this alias and wants to live a normal life.
Meet Jesús Aceves, a 55-year-old man born with a condition called hypertrichosis, which means he has abnormal hair growth over his body, especially his face. Although married with kids, Jesús isn’t fully happy with his living conditions. He says he and his family suffer discrimination. In an interview, one of his kids mentioned, “People call me names, and they even tell their kids not to be my friends.”
© Chuy, El hombre lobo / Chuy, The Wolf Man / Facebook
He worked in the circus all his life, traveling through several cities. But now, he’s tired of being seen as a freak. As a consequence of years on the road, he’s been known as The Wolf Man.
Back home and not in the circus anymore, he’s facing another challenge: finding a “normal” job. He needs to support his family since his wife works in temporary jobs.
After several failed job interviews, he agreed to try something he had always avoided: shave his face. He relied on his family barber to transform him, even creating eyebrows and lashes.
The experience was difficult since the face is an extremely sensitive body area, but both he and his wife believed that simply by shaving, he would be able to find a job.
Jesús did several interviews, and it’s confident that now he’ll find somewhere to work besides the circus. If this happens, he must shave his face every 2 days.
Although rare, some conditions aren’t impossible to have. Luckily, people find a way to overcome the difficulties a rare condition brings and strive in life. Hannah Tyre, for example, was born with osteogenesis imperfecta, meaning that her bones break very easily. But her love for makeup made her an internet influencer, reaching millions of followers. We hope that, by reaching the mainstream media, people with genetic diseases won’t suffer more discrimination.
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