In 2012, Patricia and Dale Williams welcomed a special addition to their family: baby Redd. Amid their immense joy, they quickly noticed something unique about him—his snow-white hair, a striking feature that set him apart from other infants. When Redd was about two months old, his parents observed his eyes constantly moving from side to side, which sparked concern.
Worried, they searched online for information and suspected that Redd might have albinism. Determined to find answers, they scheduled appointments with optometrists and genetic specialists. Their suspicions were confirmed when Redd was diagnosed with Oculocutaneous Albinism Type 1 (OCA1), a rare condition affecting only 1 in 17,000 people worldwide.
Initially, the hospital staff marveled at Redd’s unique appearance, expecting his hair color to change as he grew older. However, after the diagnosis, Patricia realized that Redd’s distinctive white hair and blue eyes, which occasionally shimmered red in certain lights, would be a permanent part of his identity.
In 2018, the Williams family welcomed another son, Rockwell, who also shared Redd’s condition.
Despite their parents’ efforts to instill confidence, both Redd and Rockwell faced adversity at school, enduring teasing and bullying due to their appearance. Their older brother, Gage, who does not have albinism, became their protective shield, but the challenges persisted.
The family faced a distressing incident when a photo of Rockwell shared on social media turned into a meme and spread rapidly across the internet despite their pleas for its removal.
Refusing to let negativity overwhelm them, Patricia and Dale chose a different path—they became advocates, driven by a mission to raise awareness about albinism. Patricia’s social media platform grew significantly after Rockwell’s photo went viral, prompting numerous inquiries that revealed the widespread lack of understanding about albinism in society.
Redd underwent corrective eye surgery for his strabismus, transitioning from a specialized school for visually impaired children to a public institution. This decision significantly improved Redd’s life; the family opted for surgery over eye patches to minimize attention and reduce bullying.
On April 28, 2023, Patricia shared a heartwarming video of Rockwell participating in his school’s “Western Day.” This time, the response on social media was overwhelmingly positive, contrasting starkly with the past instances of name-calling and ridicule.
Today, both Redd and Rockwell are thriving in their own unique ways.
Consider sharing this story to spread awareness and support for individuals with albinism among your family and friends.
61-year-old Meg Ryan makes rare public appearance, sparks debate on internet – ‘what did she do to herself’
The Sleepless in Seattle Star, who made her on-screen debut in Rich and Famous (1981), displayed an incredibly smooth complexion, once again fueling rumors that she may have dabbled in plastic surgery, despite her previous denials.
Indeed, some shared less than flattering opinions over Meg’s new look online, reigniting a debate that the actress herself has weighed in on in the past.
“This is Meg Ryan,” one Twitter user commented. “Hopefully women will learn from this. Plastic Surgery is for Frankenstein.
“Meg Ryan spent thousands to make herself unrecognizable and hideous,” another added.
Another person wrote of the pictures, “what did she do to herself? These hollywood elites overdo the plastic surgery. Get a refund”
“Wtf has Meg Ryan done to her face?!” a third wrote.
n the past Ryan has insisted that she pays little attention to those offering negative opinions as to her appearance.
In a 2015 interview with Porter Magazine, she openly addressed the rumors regarding plastic surgery.
“I don’t pay a lot of attention, frankly,” she said at the time. “There’s a lot of hatred in the world today. It’s so easy to judge. Imagine being a hater, how stupid.”
Turning out for the aforementioned screening, held at the Alice Tully Hall in the Lincoln Center, New York, the actress seemed to be in good spirits as she posed for pictures with the likes of Billy Murray and Elvis Costello on Michael J. Fox’s big night.
Fox, who recently conceded that he didn’t think he would live to see 80 years old, is releasing a new documentary focusing on his life during the three decades since his diagnosis.
The Back to the Future star was first told he had Parkinson’s disease aged just 29. Despite initially endeavoring to hide his condition, he’s since become a leading figure in the fight for heightened awareness and research.
In a tear-jerking recent interview, Fox candidly reflected on his own mortality, saying that his ongoing battle with Parkinson’s was “getting tougher”
“I’m not gonna lie. It’s gettin’ hard, it’s gettin’ harder. It’s gettin’ tougher,” the retired actor said. “Every day it’s tougher. But, but, that’s, that’s the way it is. I mean, you know, who do I see about that?”
He added that he recently had spinal surgery after a tumor was found on his spine. While it was benign, it affected his ability to walk, and he was injured after a fall.
“[I] broke this arm, and I broke this arm, I broke this elbow. I broke my face. I broke my hand,” Fox said.
“You don’t die from Parkinson’s. You die with Parkinson’s. I’ve been thinking about the mortality of it. … I’m not gonna be 80. I’m not gonna be 80.”
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