Angelina Jolie looked flawless as she attended the Broadway opening night of her musical, The Outsiders. The 48-year-old actress was all smiles as she posed with her 15-year-old daughter, Vivienne, who had worked with her on the project.
Jolie looked stunning in a shiny gold dress paired with a rusty-colored cape while her teenage daughter rocked a cool blue jumpsuit.
The Oscar-winning actress who worked as executive producer on the project had once revealed that Vivienne had a passion for theatre, saying, ’’She’s very thoughtful and serious about theatre and working hard to best understand how to contribute.’’
The mother-daughter pair radiated joy as they attended the event with all eyes naturally drawn to Jolie, who looked absolutely stunning with her vibrant red lipstick and slightly lighter blonde hair than her usual style.
Online, fans showered the star with compliments, saying that her beauty makes her «stand out from the crowd» and naming her «one of the world’s hottest women.» One person even noted, ’’She does look gorgeous here, even better than years ago.’’
While almost everyone would agree that the Maleficent actress looks incredible, many people noticed that there was something different about her, leaving some questioning whether her ever-growing glow was due to recent beauty procedures.
One person stated, «Angelina looks different. Or am I crazy?» While another wrote, «Looks like Angie had a little facelift or some kind of plastic surgery.» A third person added, ’’Angelina looks strange.”
Another actress who has recently caught everyone’s attention on the red carpet is Dakota Johnson. Check out her fabulous daring look here, which certainly didn’t leave anyone indifferent.
Preview photo credit MM/ABACA/Abaca/East News, MM/ABACA/Abaca/East News
How Tessa Evans is Turning a Rare Condition into a Source of Inspiration and Change
The human body’s ability to adapt and overcome challenges is truly remarkable. Tessa Evans, born on Valentine’s Day in 2013, exemplifies this resilience. Diagnosed with Bosma arhinia microphthalmia syndrome—a rare genetic condition—Tessa has not only become a symbol of medical advancement but also a beacon of hope and inspiration.
Understanding a Rare Genetic Condition
Bosma arhinia microphthalmia syndrome affects the development of the nose, eyes, and puberty, and can also influence brain structure. With fewer than 100 documented cases worldwide, the condition is exceptionally rare. First identified in Vietnam in 1981, evidence suggests its existence may date back even further. Tessa Evans is one of the few individuals living with this condition, representing a unique story of courage and progress.
A Trailblazing Journey
Tessa’s parents, Grainne and Nathan Evans from Maghera, Northern Ireland, were unprepared for the diagnosis, as no abnormalities were detected during pregnancy. Despite the shock, the couple embraced their daughter’s uniqueness and embarked on a mission to enhance her quality of life through groundbreaking medical treatments.
Groundbreaking Treatments
At just two weeks old, Tessa underwent her first surgery to receive a tracheostomy tube, enabling her to breathe and eat more easily. By the age of two, she made history as the youngest patient to receive a cosmetic nasal implant. Utilizing advanced technologies such as 3D printing and medical tattooing, doctors are working to create a permanent nasal structure for Tessa as she grows. These innovations are designed to reduce the need for future surgeries and provide her with a more natural profile.
Challenges Beyond Appearance
Living without a sense of smell presents unique safety challenges for Tessa. Without this critical sensory warning system, she is more vulnerable to dangers like fires or spoiled food. Her parents remain vigilant, ensuring her safety and emphasizing the importance of raising awareness about her condition.
Inspiring Change and Progress
Tessa’s courage and her family’s determination have sparked hope for others facing similar diagnoses. Her groundbreaking treatments have inspired another child in the UK to pursue similar procedures. Described as “charming” and “fearlessly courageous,” Tessa continues to challenge perceptions and drive innovation in medical science. Her family’s Facebook page, Tessa; Born Extraordinary, documents her incredible journey, inspiring nearly 10,000 followers.
A Legacy of Resilience
Tessa Evans’ story is one of love, resilience, and medical breakthroughs. Despite the extraordinary challenges posed by her rare condition, she exemplifies what is possible with determination and the support of a dedicated family. Tessa’s journey is not only reshaping lives but also redefining the boundaries of medical science.
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