In an astonishing testament to his unique spirit, Quest Gulliford, a TikTok sensation known for his resilience as a cancer survivor and adorned with a vast array of tattoos, is capturing attention with his latest viral video. Not only does he reveal his intricate full-body artwork, but he also showcases his bold choice of dyeing his eyes.
Having triumphed over Hodgkin’s Lymphoma, Gulliford has poured a staggering $70,000 into his tattoo collection since embarking on his inked odyssey in 2009. His recent TikTok post provides an immersive glimpse into his journey, particularly highlighting the intense mental preparation required for undergoing eyeball tattooing.
Reflecting on the risks involved, Gulliford emphasized: “It was a gamble, but one that I had been longing for… and I’m still absolutely delighted with the outcome three years down the line”.
His dedication to his distinctive mode of self-representation surpasses the $70,000 mark, with an eye-popping $10,000 designated solely for the metamorphosis of his gaze.
Recalling the mental endurance needed during the eyeball tattoo session in Houston, Texas, Gulliford confessed: “It was quite the internal battle, even after stepping foot into the studio, to muster the courage to proceed”. This nonconformist process entails a needle traversing all angles of the eyeball, resembling more of an alteration or enhancement than a conventional skin-deep tattoo.
In an unexpected development, Gulliford unveiled his intention to revisit the same tattoo artist next month, signaling his unwavering dedication to exploring the boundaries of self-expression.
Amidst the intricate tapestry of ink decorating his body, Gulliford proudly bears symbols of his victorious battle against cancer. From the inaugural tattoo, a cross etched on his chest bearing the inscription ‘God First’, to a poignant purple ribbon commemorating his seventh-grade confrontation with Hodgkins Lymphoma, each design narrates a tale of resilience.
Reflecting on the health journey that inspired his tattoos, Gulliford recounted: “I noticed a sizable lymph node… I didn’t think much of it. It led to about six months of chemotherapy. After that, I felt like I possessed superhuman strength”.
During a candid conversation with Inked magazine in 2019, Gulliford shared his venture into facial tattoos, a decision made at the tender age of 18, much to his mother’s initial dismay. Though she gradually came to terms with smaller facial inkings, the prospect of larger designs on a more prominent canvas sparked her concerns, leading to interventions at tattoo parlors in hopes of dissuading artists from executing extensive facial artwork.
Quest Gulliford’s unabashed odyssey of self-expression, forged through trials and tribulations, continues to enthrall audiences, underscoring the notion that sometimes, the most extraordinary tales find their canvas on our skin.
A baby with a rare skin disorder is born after an urgent C-section by medical professionals.
Throughout the nine months of pregnancy, a mother’s heart is filled with anticipation, excitement, and a hint of doubt. When an expecting parent gives birth, they all want the child to be healthy and happy. Regretfully, our expectations are not always met by the way things work out.
Jennie Wilklow, of Highland, New York, was looking forward to meeting her daughter. Jennie and her spouse were overcome with happiness the moment they held their baby.
After multiple ultrasounds and check-ups with the physician, the results consistently showed a healthy baby.
This assurance put their minds at rest, and they had no idea that their darling Anna would be born with a disease that would permanently alter their lives.
At 34 weeks, Jennie had a C-section to deliver Anna. She peered into Anna’s eyes when the physicians placed the baby in her arms and felt an overwhelming sense of love.
Everything was going fine with their cute little one. However, Jennie couldn’t help but feel apprehensive about her husband when he came to visit her.
Jennie told Cafe Mom, “My husband’s silence scared me.” I pressed him for additional information as the doctor was leaving the room, and he just sat there looking shocked. With remorse, he added, “It’s bad.”
Upon meeting her gaze, her spouse said, “Jennie, she has the most beautiful soul.” Jennie did not know what such terms meant at the moment. Her mind was racing, but she had no idea what was wrong.
Anna suffered from an uncommon disease known as harlequin ichthyosis, which showed up as thick, severely fractured diamond-shaped plates. Jennie said to Cafe Mom shortly after giving birth, “Her delicate skin hardened as they desperately tried to help her.”
The dramatic splitting that followed the hardening left her slathered in open wounds throughout her body.”Anna prevailed despite the physicians’ concerns about her prognosis. She was quite beautiful,” Jennie proudly declared.
Unfortunately, there is no known cure for harlequin ichthyosis. The treatment involves regular showering and thorough skin moisturization, which takes consistent effort. I used to bathe her for hours every few hours, slathering her in Vaseline.
It might not seem like much, but it was one of the things I struggled with the most. I had visualized all the amazing clothes my child would have,” Jennie said.
She set up the “harlequin diva” Instagram page and started posting images of Anna there in an effort to raise awareness of this illness. Through her articles, she sheds light on the challenges faced by parents of children with harlequin ichthyosis on a daily basis.
“Anna won many people’s hearts and is the pinnacle of perfection in its purest form.” She has a natural capacity to carry out these mundane tasks. The world celebrates with us every time we achieve a new milestone, Jennie said to Cafe Mom.
She went on, “I now realize that my love for my daughter is the reason Anna was given to me.” Because we were destined to be together, we will work together to redefine what true beauty means to the world.
In addition to being beautiful in her own right, Anna is fortunate to have parents who will stop at nothing to ensure that she has a happy existence.
Let’s help spread the news about Anna’s story by inviting our friends and family to read this article on Facebook. Despite our differences, we can work together to raise awareness of and respect for the incredible beauty and power that each individual holds.
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