Even though twins aren’t that rare, people are always intrigued by how two people can look so alike.
I’m fascinated by it too…
But Megan and Morgan didn’t just catch people’s attention because they looked alike. When they were four years old, their eyes were so clear they looked like crystal water. Once their photos were shared online, they quickly went viral.
Megan and Morgan Boyd, known as the “Trueblue Twins,” became famous when they were just four years old. Their mom shared photos of them on Instagram, and people around the world fell in love with their unique look.
While most parents enjoy showing off their kids’ pictures, these twins caught global attention. Now, they have over 153,000 followers on Instagram.
It’s easy to see why, isn’t it?
The girls were born on June 6, 2011.
Their mom, Stephanie, came up with the nickname “Trueblue Twins” because of their special blue eyes.
If you want to tell Megan and Morgan apart, just look at their eyes—they’re the key to distinguishing them.
It’s only Megan who has two blue eyes. Morgan’s right eye is not blue, but dark brown and thus bears a completely different look.
This is how the girls look today at nine years old.
Many twins often wear matching outfits, and the Trueblue Twins are no exception.
Their mom, Stephanie, loves shopping for clothes for her daughters and keeping their wardrobes current.
She thinks it’s important for her twin daughters to look and feel great.
Many people are amazed by the girls’ rare blue eye color.
Some folks might think African-American adults with blue eyes are wearing colored contacts, but it’s possible to be born with a rare gene that gives blue eyes.
Stephanie, the Trueblue Twins’ mom, also has blue eyes, and she says she doesn’t wear colored contacts.
Everything indicates that these lovely sisters will grow up to be beautiful women. Feel free to share this story if you believe the same.
Meet Twins with the Rare Benjamin Button Syndrome, Who Became Symbols of Resilience
In a small Brazilian town, there resides an extraordinary duo of identical twins named Elis and Eloá. Their story serves as a beacon of resilience and the remarkable power of the human spirit. Afflicted with Hutchinson-Gilford Progeria Syndrome, a rare and fatal genetic disorder causing accelerated aging, these twins confront their adversities with remarkable grace and strength, earning admiration from people worldwide.
Understanding Hutchinson-Gilford Progeria syndrome
HGPS stands as an exceptionally rare disorder, impacting roughly 1 in 20 million newborns globally. Marked by rapid aging from early childhood, individuals with progeria often display growth delays, diminished body fat and hair, prematurely aged skin, joint stiffness, and severe cardiovascular issues. Typically, those with HGPS have an average life expectancy of about 14.5 years, though some may extend into their late teens or early twenties. This syndrome gained public attention through the film The Curious Case of Benjamin Button.
The condition is caused by a mutation in the LMNA gene, which produces the lamin A protein responsible for maintaining the structural integrity of the cell nucleus. The mutation results in the production of an abnormal version of the protein, called progerin, which causes cells to become unstable and die prematurely.
Elis and Eloá’s journey
Elis and Eloá swiftly captured attention because of their distinctive medical condition. Despite the physical hurdles imposed by progeria, their contagious smiles and steadfast optimism have emerged as beacons of hope and inspiration. Guilherme and Elismar, the twins’ parents, have dedicated their lives to offering the utmost care for their daughters, striving to ensure they experience as normal a life as feasible within the confines of their condition.
The family’s path has been far from easy. Their daily life is filled with demanding medical routines, including physiotherapy, aimed at addressing joint stiffness and preserving mobility. Despite these challenges, Elis and Eloá approach each day with remarkable bravery and an unparalleled enthusiasm for life, which is truly remarkable.
A global community of support
Elis and Eloá’s narrative has touched hearts worldwide, sparking a surge of solidarity from individuals and groups committed to promoting awareness about progeria and backing research endeavors. The Progeria Research Foundation, a pivotal entity in this realm, has played a vital role in propelling research forward and furnishing assistance to families grappling with the condition.
Through social media platforms, the twins’ journey is shared with a broad audience, fostering a sense of community and solidarity. Their family’s updates, documenting both the highs and lows of their daily lives, provide invaluable insights into the realities of living with progeria, while also spreading a message of hope and perseverance.
Advances in research and hope for the future
In recent years, there have been remarkable advancements in comprehending and addressing progeria. A notable milestone occurred in 2020 when the U.S. Food and Drug Administration (FDA) granted approval for the first progeria treatment: lonafarnib. This medication has demonstrated efficacy in prolonging the lives of children with progeria by mitigating the accumulation of progerin in cells, thereby decelerating the disease’s advancement.
Though a cure remains elusive, ongoing research presents promising prospects. Scientists are delving into gene-editing methodologies, like CRISPR, as potential means to rectify the genetic mutation at its root. For families such as Elis and Eloá’s, these breakthroughs offer a ray of hope for the future.
And in our other article, we recounted the remarkable story of a girl born without a nose, affectionately dubbed “Voldemort,” who refuses to let her differences define her.
Leave a Reply