I had planned it for months. Every extra shift, every skipped luxury, every penny saved went towards that little box. It wasn’t the biggest diamond, I knew that. But it was elegant, minimalist, exactly what I thought she’d appreciate. It felt like us – understated, genuine, built on something real, not flashy. I was so proud of it, so proud of the effort, so hopeful for the future it represented.
The moment arrived, the words tumbled out, earnest and heartfelt. I opened the box, my heart pounding with a mixture of nerves and pure, unadulterated love. And then, she looked at it. Not at me, not at the significance of the gesture, but at the ring itself.
Her reaction wasn’t joy, or tears, or even surprise. It was a dismissive glance, a slight frown, and then, she took the box from my hand and tossed it aside. “The diamond is too small,” she said, as if commenting on a minor imperfection in a piece of furniture.
My world tilted. The air left my lungs. Broken. That’s the only word that comes close. I felt utterly broken, exposed, and profoundly helpless. All the effort, all the love, all the hope – reduced to the size of a stone. It wasn’t just the ring she had rejected; it felt like she had rejected me, the part of me that had worked so hard, that loved her enough to offer everything I had. Her words, her casual dismissal, crushed me in a way I hadn’t thought possible.
I don’t remember exactly what I said, or if I said anything at all. I just remember the feeling of numb disbelief as I bent down, picked the small, rejected symbol of my love from the floor, and walked out.
Now, days later, my phone is a constant buzz. Her name flashes across the screen, message after message, call after call. She wants the ring back. Her ring, she calls it.
But honestly? Looking at the ring now, it doesn’t represent a future together anymore. It represents that moment, that crushing realization, the feeling of being utterly unseen and unappreciated. The desire, the hope, the love I felt in that moment of proposal – it’s gone. Washed away by the cold, hard truth of a diamond that was “too small.” I’m not interested anymore. Not in the ring, and not in trying to rebuild something that shattered so completely over something so superficial.
“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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