John Amos, the talented television actor recognized for his performances in The Mary Tyler Moore Show, Good Times, The West Wing, and Roots, has passed away at the age of 84.
His family shared that Amos died of natural causes in his Los Angeles home on August 21, but the announcement was only made public today.
“With deep sadness, I announce that my father has transitioned,” his son, Kelly Christopher Amos, said in a statement to Deadline. “He was a man with an incredibly kind heart and a golden spirit… loved by people everywhere. Many fans regarded him as their TV father.”
Born on December 27, 1939, in Newark, New Jersey, Amos initially pursued a career in football, playing in the Continental Football League and the Atlantic Coast Football League. He was signed by the Denver Broncos in 1964 but was released before the season due to an injury.
His acting career, however, proved more successful. He gained recognition as weatherman Gordy Howard on the popular sitcom The Mary Tyler Moore Show, a role he held from 1970 to 1973.
Amos is best remembered for his portrayal of James Evans, the father in the classic sitcom Good Times. At just 34 years old when he was cast, he convincingly depicted a hardworking father of three living in a low-income housing project.
The show was lauded for its exploration of significant issues like poverty and racism. However, as the series progressed, Amos had disagreements with the writers and producers regarding the portrayal of Black families and the show’s shift toward broader comedic themes. After season 3, he was let go, and his character met his end in a car accident.
Shortly thereafter, Amos took on another defining role as the adult Kunta Kinte in the groundbreaking miniseries Roots, for which he received an Emmy nomination.
He is also known for his role as Admiral Percy Fitzwallace, Chairman of the Joint Chiefs of Staff, in the political drama The West Wing. Additionally, he had recurring roles in Two and a Half Men and The Ranch.
Among his notable film credits are Sweet Sweetback’s Baadasssss Song, Die Hard 2, Coming to America, and its sequel.
“He led a fulfilling life, and his legacy will endure through his remarkable contributions to television and film,” his son expressed in the statement. “My father cherished his work as an actor throughout his life.”
“He was my father, my closest friend, and my hero. I appreciate your prayers and support during this difficult time.”
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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