Fast forward to the present, and there’s a renewed interest in Bruce Willis’s career, specifically his iconic role in the 80s TV show “Moonlighting.” The show, also known as “Maddie & David,” has made a comeback on a streaming platform, thrilling fans worldwide. Glenn Gordon Caron, the creator of the series and a close friend of Willis, shared some touching insights about their recent interactions.
Glenn revealed that he has seen Willis’s health decline rapidly. Despite this, Willis remains enthusiastic about the comeback of “Moonlighting.” Glenn confessed that he tries to maintain regular contact with his dear friend and his family, acknowledging the significant impact the illness has had on Willis’s life.
Although Bruce Willis’s condition has affected his ability to communicate verbally, Glenn acknowledges that the essence of Willis remains intact. Glenn marvels at Willis’s recognition when they meet and describes him as a truly remarkable individual. Though he may have lost some linguistic abilities, Glenn emphasizes the enduring spirit of Bruce Willis.
In an interview with the New York Post, Glenn shared his admiration for his friend, highlighting the immense joy for life that Willis possessed. Each day brought enthusiasm and a zest for living to the fullest. It is this spirit that captivated those fortunate enough to spend time with him.
A Journey Filled with Love and Compassion
Bruce Willis’s wife, Emma Heming Willis, has been a pillar of strength throughout his battle with illness. In a recent appearance on the Today show, she bravely discussed the impact of dementia, both on the person diagnosed and their loved ones. Emma, who has two daughters with Bruce, emphasized that receiving a dementia diagnosis is a challenging experience for the entire family.
Emma admits that uncertainty clouds Bruce’s awareness of his illness. However, she finds solace in being the primary caregiver and having a comprehensive understanding of the disease. While it is undoubtedly painful, Emma sees it as both a blessing and a curse – a way to navigate this difficult journey alongside her husband.
Born without a nose: This is what Tessa Evans looks like at 10 years old
Tessa Evans, who was born on February 14, 2013, was born without a nose, a rare condition that has sparked admiration and affection from her family and people around the world.
Tessa’s unique condition is known as Bosma Arhinia Microphthalmia Syndrome (BAMS) and there are fewer than 100 documented cases worldwide. Despite the rarity and complexity of her condition, her mother praises Tessa’s “charming” behavior and her “remarkable courage”.
Eight years into her journey, Tessa has become a symbol of resilience. She continues to do well and embrace life to the fullest, despite the challenges presented by her condition, which includes the inability to smell or breathe through her nose.
However, she can still cough, sneeze and catch colds. “It was pretty amusing the first time she sneezed”, recalls her father Nathan, “but we realized it was actually coming from her chest, which was a small but reassuring sign of normality”.
Tessa’s parents, Grainne and Nathan Evans, were stunned when their Valentine’s baby was born without a nose as the pregnancy was uneventful and there were no signs of problems.
A native of Maghera, Ireland, Tessa’s condition required immediate medical intervention. At less than two weeks old, she underwent surgery to insert a tracheostomy tube so she could eat and sleep comfortably.
At just two years old, Tessa achieved a medical milestone when she became the first person to receive a cosmetic nasal implant, marking a significant advance in the field and a remarkable solution to her rare condition.
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