In 2011, Catherine, Princess of Wales, wore a second stunning wedding dress to celebrate her marriage to Prince William. But only 300 guests saw it.
Thirteen years ago, Kate Middleton captivated the world as she walked down the aisle with her father, wearing a breathtaking wedding gown designed by Sarah Burton for Alexander McQueen.
While her first dress made global headlines, Kate also wore a second dress at a private evening reception. According to a royal expert, this dress reflected how she truly wanted to express herself. Kate chose the British McQueen brand for its craftsmanship and respect for traditional workmanship.
The Palace stated at the time that she wanted a gown that combined tradition and modernity with the artistic vision of Alexander McQueen. The first dress, made of elegant French Chantilly and English Cluny lace, cost a staggering £250,000 and became an iconic symbol of her wedding day. However, her second dress, though less publicized, was just as special.
Stylist and royal fashion expert Miranda Holder explained that some royals change into a second wedding dress after the ceremony. This allows them to leave behind formalities and fully express themselves. Speaking to The Express, she said that having a second dress allows brides to show who they really are and how they want to feel after the formal ceremony and official photos.
Kate’s second look, while still formal, was simpler and more relaxed. Holder described it as “simple and sweet,” with a “very pretty” cardigan, but noted that Kate didn’t seem to have the chance to fully relax.
Which dress do you prefer? Here’s where you can find the secret message Princess Catherine hid in her look during her first public appearance after cancer treatment.
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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