After Luke Bryan, a musician, lost his voice while supporting the Georgia Bulldogs during the National Championship game versus the Alabama Crimson Tide on January 10, his fans came together to offer him their well wishes.
Emotions were running high as Georgia won their first championship in more than 40 years, and the game was fierce. In the midst of the excitement, Luke Bryan ended up losing his voice.
Luke Bryan’s physician has directed him to take vocal rest till further notice in order to promote a quick recovery. In typical Luke Bryan style, the “That’s My Kind of Night” singer is preparing for his next gigs at Crash My Playa in Mexico while taking this time to heal.
Luke and his spouse Caroline laughed at the circumstances and posted a lighthearted picture to social media. Caroline joked that she was driving Luke nuts by talking nonstop while he was mute when she shared a picture of herself appearing to tape Luke’s lips shut. Fans were overwhelmingly supportive of their playful banter, with many of them being able to relate to the situation.
When Chase Chrisley from the reality series “Chrisley Knows Best” got in on the prank, the good times got even better. “Send the tape to my mom, I can tell you she wants it for my dad,” he said in a lighthearted manner. It appears that many people who have gone through similar experiences in the past have found solace in Luke Bryan’s voice loss.
Even though Luke is currently unable to sing, he is still aggressively promoting his just released “Up” music video. He looks content in the video and asks his followers to offer prayers for his voice while he takes a vocal break. Supporters have shown their steadfast loyalty by posting heartfelt messages saying how excited they are to party with him at Crash My Playa in Cancun.
Luke Bryan’s voice might be muted for the time being, but his passion and commitment to his craft never waver. Let’s all hope he heals quickly so we may enjoy his incredible performances once more.
A baby girl who ‘never stops smiling’ is living with a rare skin condition that makes her skin crack
Those nine months a mom carries her baby are filled with joy, anticipation, and a dose of uncertainty. What the new parents hope for is their bundle of joy to be healthy. Sadly, that is not always the case.
Jennie Wilklow, from Highland, New York, couldn’t wait to meet her daughter. She and her husband were over the moon to hold her in their arms. All the ultrasounds and doctor’s appointment suggested the baby was healthy, so they were eased and never thought sweet Anna would be born with a condition that would change all of their lives forever.
Jennie delivered Anna via C-section at 34 weeks. Doctors told her she looked beautiful and that was all Jennie needed to hear at that point.
Shortly after, the proud mom heard her daughter cry, and that was just another sign that everything was right with her little jewel.
When her husband visited Jennie, he was strangely silent and looked worried and puzzled.
“My husband’s silence scared me; he just sat in shock as the doctor left, and I prodded for more info,” Jennie shared with Cafe Mom.
“He just kept saying, ‘It’s bad.’ What does that even mean? I thought in my head. He told me, ‘Jennie, I looked in her eyes, and she has the most beautiful soul.’”
Anna was diagnosed with harlequin ichthyosis, a rare condition that causes thick diamond-shaped plates that are separated by deep cracks. “As they tried frantically to help her, her skin hardened within seconds (of birth). After hardening, it began to split, causing open wounds all over her body,” Jennie told Cafe Mom.
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Although doctors weren’t sure she would survive, Anna beat the odds and is thriving. “She was beauty in the purest form,” her mom said.
There isn’t cure, and the treatment is quite demanding as it requires constant baths and keeping the skin as much moisturized as possible. “Every couple of hours I covered her with Vaseline and bathed her for many hours of the day. I had dreamed for years about the things my baby would wear, and though it seemed so trivial, it was what I struggled with most,” Jennie said.
In an attempt to raise awareness about this condition, Jennie posts photos of Anna on her Instagram page harlequindiva. She opens up about the everyday struggles and what it is like to have a child with harlequin ichthyosis.
“Anna captured everyone’s hearts because she is the purest form of perfection. Doing the work every day is simple when I’m doing it for her, and with every new accomplishment, the world celebrates with me,” Jennie told Cafe Mom.
She adds, “I now understand that I was given her because of the love I already carried in my heart for my daughter. Anna was meant for me, and I for her, and together we will show the world what true beauty is.”
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