My husband and I bought our granddaughter Eloise a wedding gift from her registry, but she accused us of being cheap. She expected the $40,000 cash gift we give our grandkids before their weddings. Upset, she threatened to cut us off.
“We buy a small gift from the registry and give a check for $40,000 the day before the wedding,” I explained. This time, we sent an air fryer, the cheapest item on her list. Eloise called, livid: “An air fryer? That’s the cheapest thing you could find?”
I told her, “Yes, we’re cheap, old, and useless. The only thing you didn’t know is that the day before the wedding, we were going to gift you a check for $40,000.”
Eloise’s reaction made us reconsider giving the cash. Later, she found out about our tradition and accused us of discrimination. “Why didn’t I get anything?”
“We felt after your reaction, it wasn’t right to go ahead with the gift,” I said. Eloise, now boycotting Christmas, refuses to understand our perspective. Despite this, our door and hearts remain open to her.
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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