Richard David Hendrickson, president and CEO of Lifetime Products, and his 16-year-old daughter Sally were killed in a tragic accident in Ogden Canyon on Saturday.
According to the Utah Highway Patrol, they were killed instantaneously when a truck’s excavator broke loose and fell over their pickup truck.
The tow truck was navigating a tight right-hand curve while pulling a small bulldozer when the tragedy occurred. After breaking loose, the bulldozer crashed into Hendrickson’s GMC pickup. Two other adult passengers suffered non-life-threatening injuries, and Hendrickson and Sally were both pronounced dead at the site. Hendrickson was honored by Lifetime Products, which described him as more than just a business leader.
They emphasized his wide range of skills, renowned mechanical prowess, and remarkable interpersonal skills. In addition, Hendrickson was the Church of Jesus Christ of Latter-day Saints’ stake president.In addition to expressing his sympathies for X, Utah Governor Spencer Cox offered prayers for the bereaved family and lamented the passing of his friend and leader.Many people in the neighborhood are grieving the loss of Hendrickson and his daughter as a result of this unfortunate incident.
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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