Fans are devastated at the news that Frank Fritz, the antiques expert who gained fame on the reality series American Pickers, has died at 60.
Fritz, who left the series in 2021, had been suffering from health problems and was hospitalized from a stroke two years ago.
The news was announced by Fritz’s friend and co-star Mike Wolfe, who said that Fritz passed away last night.
“I’ve know Frank for more [than] half my life and what you’ve seen on TV has always been what I have seen, a dreamer who was just as sensitive as he was funny,” Wolfe wrote in a social media tribute. “The same off camera as he was on, Frank had a way of reaching the hearts of so many by just being himself.”
Fritz and Wolfe gained fame as the hosts of the reality TV series American Pickers, which premiered on the History Channel in 2010. The series showed the two “pickers” traveling across the USA, searching for valuable antiques and collectibles in unexpected places.
“We’re looking for amazing things buried in people’s garages and barns,” the show’s opening narration explains. “What most people see as junk, we see as dollar signs. We’ll buy anything we think we can make a buck on.”
“We make a living telling the history of America… one piece at a time.”
The series attracted millions of viewers, becoming one of History Channel’s most popular programs. In its debut year it was the #1 non-fiction series among total viewers and adults 25-54.
While the antiques were often interesting, there’s no doubt it was the chemistry and charisma of the two hosts that kept viewers coming back for more.
In 2021, it was announced that Fritz would be leaving American Pickers after a decade on the hit series. Fritz said the decision was not his own, and that he was pushed out by the network after a back surgery.
“I didn’t leave the show,” he told The Sun at the time. “I finished shooting and then I had a little back surgery and the pandemic came.”
He also suggested that his co-host’s ego was a factor, saying the show had “tilted towards him 1,000 percent.” “I haven’t talked to Mike in two years,” Fritz said. “He knew my back was messed up, but he didn’t call me up and ask how I was doing. That’s just how it is.”
In July 2022, Fritz was hospitalized from a stroke. In 2023, he had a tearful reunion with Mike Wolfe, and the two resolved their purported feud. However, Fritz declined an offer to rejoin American Pickers, deciding to focus on his health.
It’s clear that the two former co-hosts have remained friendly since then, and it seems Wolfe was by his side til the end.
“We’ve been on countless trips and shared so many miles and I feel blessed that I was there by his side when he took one last journey home,” Wolfe wrote on Instagram. “I love you buddy and will miss you so much I know [you’re] in a better place.”
American Pickers remains a staple of the History Channel lineup. Fritz has never officially been replaced as co-host, though series regulars like Danielle Colby, Mike Wolfe’s brother Robbie, and friend and antiques expert “Jersey Jon” Szalay will rotate accompanying Wolfe on his antiquing trips.
Colby also shared her own tribute to Fritz on social media. “Frank, I will miss your ability to make everyone laugh, your love for talking tattoos, your epic collections but what I will miss the most are those little glimpses of vulnerability from time to time,” she wrote.
“Frank, you loved your cat and your momma and we bonded on those things. You will be missed for all of these reasons and so many more.
Rest in Peace Road Dog.”
Rest in peace to the iconic reality TV star Frank Fritz 😢🙏 Please share this story in his memory.
Meet Twins with the Rare Benjamin Button Syndrome, Who Became Symbols of Resilience
In a small Brazilian town, there resides an extraordinary duo of identical twins named Elis and Eloá. Their story serves as a beacon of resilience and the remarkable power of the human spirit. Afflicted with Hutchinson-Gilford Progeria Syndrome, a rare and fatal genetic disorder causing accelerated aging, these twins confront their adversities with remarkable grace and strength, earning admiration from people worldwide.
Understanding Hutchinson-Gilford Progeria syndrome
HGPS stands as an exceptionally rare disorder, impacting roughly 1 in 20 million newborns globally. Marked by rapid aging from early childhood, individuals with progeria often display growth delays, diminished body fat and hair, prematurely aged skin, joint stiffness, and severe cardiovascular issues. Typically, those with HGPS have an average life expectancy of about 14.5 years, though some may extend into their late teens or early twenties. This syndrome gained public attention through the film The Curious Case of Benjamin Button.
The condition is caused by a mutation in the LMNA gene, which produces the lamin A protein responsible for maintaining the structural integrity of the cell nucleus. The mutation results in the production of an abnormal version of the protein, called progerin, which causes cells to become unstable and die prematurely.
Elis and Eloá’s journey
Elis and Eloá swiftly captured attention because of their distinctive medical condition. Despite the physical hurdles imposed by progeria, their contagious smiles and steadfast optimism have emerged as beacons of hope and inspiration. Guilherme and Elismar, the twins’ parents, have dedicated their lives to offering the utmost care for their daughters, striving to ensure they experience as normal a life as feasible within the confines of their condition.
The family’s path has been far from easy. Their daily life is filled with demanding medical routines, including physiotherapy, aimed at addressing joint stiffness and preserving mobility. Despite these challenges, Elis and Eloá approach each day with remarkable bravery and an unparalleled enthusiasm for life, which is truly remarkable.
A global community of support
Elis and Eloá’s narrative has touched hearts worldwide, sparking a surge of solidarity from individuals and groups committed to promoting awareness about progeria and backing research endeavors. The Progeria Research Foundation, a pivotal entity in this realm, has played a vital role in propelling research forward and furnishing assistance to families grappling with the condition.
Through social media platforms, the twins’ journey is shared with a broad audience, fostering a sense of community and solidarity. Their family’s updates, documenting both the highs and lows of their daily lives, provide invaluable insights into the realities of living with progeria, while also spreading a message of hope and perseverance.
Advances in research and hope for the future
In recent years, there have been remarkable advancements in comprehending and addressing progeria. A notable milestone occurred in 2020 when the U.S. Food and Drug Administration (FDA) granted approval for the first progeria treatment: lonafarnib. This medication has demonstrated efficacy in prolonging the lives of children with progeria by mitigating the accumulation of progerin in cells, thereby decelerating the disease’s advancement.
Though a cure remains elusive, ongoing research presents promising prospects. Scientists are delving into gene-editing methodologies, like CRISPR, as potential means to rectify the genetic mutation at its root. For families such as Elis and Eloá’s, these breakthroughs offer a ray of hope for the future.
And in our other article, we recounted the remarkable story of a girl born without a nose, affectionately dubbed “Voldemort,” who refuses to let her differences define her.
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