The Statler Brothers Show held a significant pIace on The Nashville Network, a country-music-oriented cable network eventually folded into Paramount in 2018.
Airing every Saturday night, the show featured the immensely talented Statler Brothers. Although not biologicaI brothers, this group initially gained recognition by backing Johnny Cash from 1964 to 1972.
After years of dedication, the four men—Harold Reid, Don Reid, Phil Balsley, and Lew DeWitt—successfully ascended to fame with hits like “The Class Of ’57” and Flowers on the Wall.
With a remarkable catalog of over 40 aIbums, they garnered numerous accolades, including three Grammys, three Academy of Country Music awards, and an impressive nine VocaI Group of the Year awards from the Country Music Association, all within a span of 12 years.
They hold memberships in both the Country Music and Gospel Halls of Fame.
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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