Julia Roberts is one of the rare celebrities who lives a relatively ordinary existence. She has been married to cinematographer Daniel Moder for 19 years, and the couple appears to be extremely happy.
he couple has three children: twins Phinnaeus and Hazel, both 16, and a son, Henry, 14.
Both Roberts and Moder try to keep their children out of the public eye, which is why we rarely see them attending public events or sharing images on social media.
However, we saw Hazel in the presence of her father at the Cannes Film Festival in France in July.
The two were there to promote the film Flag Day. Moder was the choreographer, and Sean Penn, was the director.
While Penn’s children played characters in the film, Hazel did not, but she attended the ceremony to support her father’s efforts.
Hazel’s amazing beauty drew everyone’s attention.
While some claim she inherited her mother’s nose, many believe she’s a striking likeness of her handsome father, so it’s no surprise she’s attractive herself. Hazel has blonde hair and blue eyes.
She was dressed in a soft yellow long lace gown and black Mary Jane heels. Her hair was pulled back into a ponytail and her make-up was modest. A true woman!
Moder was clearly proud of his girl and spent the entire evening by her side.
Whether Hazel or her siblings are interested in pursuing professions in the film industry is unknown because their parents rarely speak about their children and prefer to keep them out of the spotlight, which is understandable given Roberts’ grounded nature.
Despite her great income, which is reported to be approximately $250 million, she has never acted like a diva and has always maintained a humble demeanor.
In 2016, Hazel and her brothers played minor roles in Robert’s film Mother’s Day.
In 2018, Roberts told Harper’s Bazaar about her children:
“I don’t think they’ll ever understand (my fame). I think I told you once that when they started figuring it out, they were like, ‘You’re famous?’”
“And I said, ‘I think a lot of people might have seen the movie that I’m in or might know who I am.’”
She then discussed the issues that today’s youngsters experience, saying, “It’s different than when I might have said to my mom, ‘Mom, you don’t know what it’s like to be a teenager today,’ even though she probably did.”
Danny and I have no idea what it’s like to be an adolescent today. When my children ask me questions, I just tell them, ‘I’m going to say no and check into it because I have no idea what we’re talking about.’”
This baby’s nickname was Pinocchio and check out what he looks like years later
From the moment little Olli Tresiz came into the world, it was clear he was unique, bearing the rare and intricate condition known as encephalocell. This distinctive trait marked the outset of a challenging journey toward finding medical solutions tailored to his needs.
As Olli’s journey progressed, his growing nose revealed a vulnerability: even minor injuries posed a grave threat, potentially triggering meningitis.
Realizing the seriousness of Olli’s situation, physicians strongly advised a crucial medical intervention to mitigate the risks associated with his condition.
Fortunately, the medical procedure proved effective, not only addressing the specific challenges of encephalocell but also significantly enhancing Olli’s respiratory capacity.
This pivotal moment marked a significant shift for the young lad, presenting him with an opportunity for a life marked by improved health and greater comfort.
In a bold act of both bravery and advocacy, Olli’s mother chose to unveil her son’s tale to the world. Taking to the vast expanse of the internet, she shared a heartfelt photo of Olli, shining a light on the rare medical circumstances that can find resolution through medical interventions.
The online community responded with an overwhelming display of solidarity, flooding the digital realm with well-wishes and hopes for Olli’s swift recovery.
This virtual embrace not only offered solace to the Tresiz family but also underscored the power of collective compassion and understanding in the face of exceptional medical trials.
Olli’s voyage, from the intricate labyrinth of encephalocell to the triumphant strides of medical intervention, stands as a testament to the strides made in medical science and the indomitable spirit of those confronting uncommon ailments.
Through the dissemination of awareness and shared narratives, Olli’s narrative has blossomed into a wellspring of inspiration, nurturing empathy and optimism within the online sphere and beyond.
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