“Absolute Nightmare”: 7-Year-Old With Rare Condition Sleeps With His Eyes Closed for the First Time
For the first time in his life, 7-year-old Carter Bresee from Nevada has been able to sleep with his eyes fully closed—a milestone most of us take for granted. Carter suffers from lamellar ichthyosis, a rare genetic skin disorder, and ectropion, which causes the eyelids to turn outward. These conditions made it impossible for him to close his eyes completely, even while sleeping.
This life-changing moment came after a successful surgery that corrected his ectropion. The procedure not only brought relief to Carter and his family but also sparked hope for others facing similar struggles.
A Rare and Challenging Journey
Lamellar ichthyosis is a condition in which the skin produces excess cells that do not shed normally, leading to thick, brown, scale-like patches. In Carter’s case, this also caused ectropion, pulling his eyelids outward due to the tightness and overgrowth of his skin.
For years, Carter had to endure discomfort, dryness, and a heightened risk of eye infections. His condition required constant care, including frequent application of ointments to keep his skin and eyes moisturized. The inability to close his eyes compounded the emotional and physical toll on him and his family.
A Community Rallies
The family turned to the community for help, launching a fundraising campaign to cover the $8,000 surgery cost. The response was overwhelming—donors contributed more than $46,000, far surpassing the initial goal. The additional funds will now help cover Carter’s ongoing medical needs, including specialized skin treatments and future surgeries.
“We were blown away by the generosity of people we’ve never met,” said Carter’s mother, Ashley Bresee. “This surgery means so much more than just being able to close his eyes—it’s a chance at a better quality of life.”
A New Chapter
Following the surgery, Carter is not only sleeping more comfortably but also experiencing improved vision and eye health. His parents describe the moment they saw him sleep with his eyes closed for the first time as nothing short of miraculous.
“This has been an absolute nightmare for our family, but now we feel like we’re finally waking up from it,” Ashley shared. “Carter is already more energetic and happier—it’s incredible to see.”
Raising Awareness
Carter’s story sheds light on the challenges faced by those living with rare genetic conditions and underscores the importance of community support and medical innovation. His journey is a testament to the resilience of families battling rare diseases and the transformative power of compassion.
For Carter, this surgery marks the beginning of a brighter future. And for the community that supported him, it’s a reminder of how small acts of kindness can create profound change.
#1 7-year-old Carter is now able to sleep with his eyes closed following a major eyelid surgery
Fox News had been following Carter’s journey for years and discovered that his condition forces his eyelids to turn outwards, making it impossible for them to close.
“He cannot blink, he sleeps with his eyes open and is often experiencing lots of pain and discomfort because of this,” wrote Shai, Carter’s mother, on her GoFundMe page when she first decided to raise funds for surgery.
The initial goal was to raise at least $8,000 for an oculoplastic surgery—which involved removing skin from a different part of Carter’s body and grafting it onto his eyelids. In the end, they received more than $46,000.
#2 tough journey
“I didn’t realize what a sense of community we really had,” she told the outlet. “It’s really crazy to feel so included.”
After the operation at UC San Diego was successful, Shai opened up about Carter’s first normal night of sleep—and boy, did it sound perfect.
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#3 The 7-year-old boy reportedly remained calm throughout the procedure and is now recovering
#4 New Eyes
Carter’s mother described him as a “champ” during the surgery, as well as the recovery process.
“He was able to play his games and he had the best attitude and didn’t complain about a single thing, even when he was in pain he said mom I think a little bit more medicine.”
Carter has since gone back to school and, although he will require follow-up appointments for the rest of his life, this surgery is expected to provide relief for the next 10 years.
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#5 Readers commended Carter online for his strength and determination
In a Reddit thread posted yesterday, commenters shared their thoughts on the boy’s journey.
“Man that sounds like living in an absolute nightmare,” one person said. “Glad he was able to get surgery for this!”
“A mother’s love is strong with this one,” another wrote.
A third user wished him “the most restful sleep and wonderful dreams every night for the rest of his life.”
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#6 The two conditions Carter was diagnosed with normally come from mutations in the patient’s genes
Although cervical ectropion is not a cause for concern, according to the Cleveland Clinic, lamellar ichthyosis is more serious.
It affects only one in every 100,000 individuals in the United States, but it’s more common in Norway, where an estimated one in 91,000 people are affected.
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#7 Disorder
The disorder occurs when the genes responsible for the proteins found in the outermost layer of the skin mutate. Abnormalities, such as the impaired regulation of body temperature, water retention, and resistance to infections, can be observed.
These mutations are the cause of 90% of lamellar ichthyosis cases. The other 10% is not as widely known, as some result from a deviation in various genes, while others are unknown.
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#8 Detailed Treatment Approaches for Lamellar Ichthyosis and Ectropion
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