Losing a spouse is an incredibly difficult experience, especially when they pass away. It brings immense grief and sadness that can be difficult to move on from. However, Kelly Rizzo, the widow of beloved Full House star Bob Saget, has shown incredible strength in facing her grief head-on.
After two years of mourning, Rizzo has decided to embark on a new chapter in her life – the world of dating. In January 2022, the world was shocked by Saget’s unexpected passing at the age of 65 due to accidental head trauma. Rizzo openly expressed her grief since then but now, she’s ready to take a step forward.
Initially, Rizzo shared that dating was not something she could even fathom, stating, “The thought of anything serious in the near future was just too complicated emotionally.” However, she also acknowledged the importance of companionship and expressed her openness to meeting someone and enjoying simple activities, such as going for a coffee or a hike.
Recently, Kelly Rizzo made her public debut with her new partner, Breckin Meyer. The couple appeared together at the Jam for Janie GRAMMY Awards Viewing Party and posed on the red carpet. Meyer is known for his roles in popular movies like Clueless and the live-action Garfield films.
Rizzo looked stunning in a body-hugging leopard-print dress, while Meyer went for a more casual look with gray khakis and a denim jacket. Their relationship has since been confirmed by the media.
It’s important to remember that healing is a personal journey, and everyone finds love in their own time. Kelly Rizzo’s willingness to open her heart again is a testament to her strength and resilience.
She had previously mentioned that dating was not something she was ready for, as the emotions attached to the idea were still overwhelming. However, she expressed her readiness to explore the possibility in the future.
As we celebrate this new chapter in Kelly Rizzo’s life, let’s also remember the love she shared with Bob Saget. They were married for four years until his passing in 2022. Moving on after losing a loved one is never easy, but we wish her the best of luck in finding happiness in whatever she pursues.
“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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