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.
Mom of rare twins with Down syndrome shuts down critics with photo showing how beautiful they are
While the chances of giving birth to twins increased 72 percent between 1980 and 2018, it’s still pretty rare. About 33 out of every 1,000 births are twins.
And what are the chances of identical twins? Approximately every three or four births out of every 1,000 are identical twins. So again, relatively rare.
When 23-year-old Savannah Combs found out she was pregnant with twins, she was thrilled. And then she learned another rarity, they both had Down syndrome.
Of course, it was emotional news. Savannah and her husband, Justin Ackerman, knew that some people would judge her and her babies because of their condition.
But to Savannah, that’s what makes them incredibly precious.
“It’s very rare what they have, but they’ve been my little gems,” she told News4JAX.
Savannah, who is from Middleburg, Florida, shared her post-pregnancy journey with her daughters Kennadi Rue and Mckenli Ackerman, on TikTok where they quickly gained a following.
In one of her videos, Savannah said she was told to abort her babies because they would not make it.
She decided to keep them and give them a fighting chance.
”Every [prenatal] appointment they were alive was a blessing to me,” Savannah explained.
When she learned they both had Down syndrome, her husband was away at boot camp.
Savannah was 29 weeks pregnant when she was admitted to the hospital, and delivered her daughters. The identical twin girls, Kennadi Rue and Mckenli Ackerman, were born on May 12, 2021.
The twins arrived two months before their due date, so they had to spend several weeks in the NICU before they came home.
They’re called mono di twins, meaning that they had their own sacs, but they shared the same placenta, meaning that they were going to be identical,” she said.
“Mo di twins as it is, it’s like very rare. And then you throw Down syndrome on top of it, it’s like one in 2 million.”
Despite their rare condition, Savannah said they are just like any other child.
“They have feelings. They have a beating heart. They know how to talk. They know how to do things you do. They will get there,” she said.
“Like I said, it may be a step behind but they’re going to do it. I’ve learned these kids are feisty little things and happy little things.”
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