Following the sudden and tragic passing of Rick Harrison’s son, Adam, the Pawn Shop’s star breaks silence posting a heartfelt tribute to Instagram.
Adam, 39, died of overdose in Las Vegas on Friday, leaving his family utterly devastated and shocked.
“You will always be in my heart! I love you Adam. 💔,” Rick wrote alongside a photo of himself smiling with Adam at a bar.
Previously, a representative of the family, Laura Herlovich, confirmed Adam’s death to the Las Vegas Review-Journal.
“Our family is extremely saddened by the death of Adam. We ask for privacy as we grieve his loss,” the statement read.
Speaking to Fox News Digital, Rick revealed the exact cause of Adam’s death saying that fentanyl was to blame.
“Yes, I can confirm Adam died from a fentanyl overdose,” the reality-show star said. “The fentanyl crisis in this country must be taken more seriously. It seems it is just flowing over the borders and nothing is being done about it. We must do better.”
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Fans, as well as some of Rick’s celebrity friends, were quick to share messages of condolence.
“I’m so sorry man,” wrote Donald Trump’s son, Donald Trump Jr.
Adam’s brother, Corey Harrison, also paid his tribute to his late sibling on Instagram, sharing an old baby photo of the two of them in a bath.
“Wax wtf I will always love you bubba,” he captioned the image.
Adam was Rick Harrison’s second child from his first marriage to Kim Harrison. Rick later went on to marry his second wife with whom he has son Jake.
While we saw Rick and Corey running the Gold & Silver Pawn and appearing on the show, Adam was not as involved, although it has been reported that he did work with his father.
The Centers for Disease Control and Prevention reports overdose deaths, including synthetic opioids, raising 56.6% from January 2020 to 2021.
The Drug Enforcement Agency lists fentanyl as a Schedule II controlled substance “that is similar to morphine but about 100 times more potent.” Depending on a person’s body, even two milligrams, which is less than a grain of salt, can be lethal.
Our thoughts and prayers go to the Harrison family.
Rest in peace, Adam.
A baby girl who ‘never stops smiling’ is living with a rare skin condition that makes her skin crack
Those nine months a mom carries her baby are filled with joy, anticipation, and a dose of uncertainty. What the new parents hope for is their bundle of joy to be healthy. Sadly, that is not always the case.
Jennie Wilklow, from Highland, New York, couldn’t wait to meet her daughter. She and her husband were over the moon to hold her in their arms. All the ultrasounds and doctor’s appointment suggested the baby was healthy, so they were eased and never thought sweet Anna would be born with a condition that would change all of their lives forever.
Jennie delivered Anna via C-section at 34 weeks. Doctors told her she looked beautiful and that was all Jennie needed to hear at that point.
Shortly after, the proud mom heard her daughter cry, and that was just another sign that everything was right with her little jewel.
When her husband visited Jennie, he was strangely silent and looked worried and puzzled.
“My husband’s silence scared me; he just sat in shock as the doctor left, and I prodded for more info,” Jennie shared with Cafe Mom.
“He just kept saying, ‘It’s bad.’ What does that even mean? I thought in my head. He told me, ‘Jennie, I looked in her eyes, and she has the most beautiful soul.’”
Anna was diagnosed with harlequin ichthyosis, a rare condition that causes thick diamond-shaped plates that are separated by deep cracks. “As they tried frantically to help her, her skin hardened within seconds (of birth). After hardening, it began to split, causing open wounds all over her body,” Jennie told Cafe Mom.
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Although doctors weren’t sure she would survive, Anna beat the odds and is thriving. “She was beauty in the purest form,” her mom said.
There isn’t cure, and the treatment is quite demanding as it requires constant baths and keeping the skin as much moisturized as possible. “Every couple of hours I covered her with Vaseline and bathed her for many hours of the day. I had dreamed for years about the things my baby would wear, and though it seemed so trivial, it was what I struggled with most,” Jennie said.
In an attempt to raise awareness about this condition, Jennie posts photos of Anna on her Instagram page harlequindiva. She opens up about the everyday struggles and what it is like to have a child with harlequin ichthyosis.
“Anna captured everyone’s hearts because she is the purest form of perfection. Doing the work every day is simple when I’m doing it for her, and with every new accomplishment, the world celebrates with me,” Jennie told Cafe Mom.
She adds, “I now understand that I was given her because of the love I already carried in my heart for my daughter. Anna was meant for me, and I for her, and together we will show the world what true beauty is.”
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