Be prepared for a surprise: Reality star weighing 600 pounds wed in a daring wedding dress

Tammy Slayton, who is overweight, opted to wear an open dress.

Tammy and Emmy Slayton are the stars of the well-known American reality show “1,000 Pound Sisters,” which follows two teenagers who are dangerously obese.

They are currently 34 and 35 years old, respectively. Up until a few years ago, they consented to broadcast their daily lives to millions of viewers in the hopes of becoming in shape and beginning to live life to the fullest.

For three seasons, the sisters struggled with their addictions and with themselves. Amy, who is losing weight and requesting surgery, was the sibling who experienced the most success.

Amy and Tammy were both at 185 and 275 kg at the time of shooting (of which Amy had already lost roughly 50 kg). In contrast to her sibling, she has gained weight and is currently close to three hundred pounds. Tammy’s health naturally soon deteriorated, and she was sent to an Ohio medical rehabilitation facility that specialized in treating obese individuals.

She is currently receiving care at the clinic for her weight loss and the pulmonary issues that her fat-related obesity caused. Tammy still feels very strongly about her life’s mission. She routinely posts funny videos to her social media accounts, updates her fans on her health, and reassures her followers that everything is well.

At the treatment center is where Tammy first met her fiancé, Caleb Willingham. That encounter marked the beginning of the only relationship she has ever experienced that wasn’t based on internet dating. The man proposed to her there after they had already staged a wedding there, where they had first met.

Many of the concerns they share may be discussed with one another. They help each other a lot now, they really do. The pals of the couple say it’s amazing.

The intimate wedding was attended by just the bride’s closest relatives and friends. This included Amy, the sister of the bride, who had lost weight and as a result was already married and had a kid.

“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.”

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.

Preview photo credit A True Story / Youtube

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