Abigail and Brittany Hensel took their first breath in 1990 as a pair of twins. These twins were a little different from others – They were conjoined. The rare case of conjoined twins caught them in a lot of limelight. They share a body but have different heads. Ever since their birth, their story has been covered by several magazines and media houses worldwide.
What are Conjoined Twins?
Conjoined twins are two babies born physically and connected to each other. They develop when an early embryo only partially separates to form two individuals. Although two fetuses develop from the same embryo, they remain connected at the different parts of their bodies, at the pelvis, abdomen, and chest. Conjoined twins may as well share one or more internal organs.
Many conjoined twins are not alive when born or stillborn. Some of them even die shortly after their birth. But the recent advancements in medical science have improved their survival rates. The doctors may perform surgeries to separate their bodies from each other.
The parents of Abby and Brittany gave a cold shoulder to this suggestion as it was risky. The sisters have become the most famous conjoined twins worldwide. They first appeared on television at the famous Oprah Winfrey Show. Back then, they were only six years old, trying to coordinate their shared body.
Here’s everything to know about the twin sisters.
Early Life of Abby and Brittany Hensel
Abigail, also known as Abby, and Brittany were born in 1990 in Minnesota and were raised by both parents in the same city. They graduated from the Mayer Lutheran High School in 2008. Afterward, the conjoined twins attended Bethel University in Arden Hills, Minnesota. They majored in their education from the said university.
The twins became college graduates by 2012 and entered the next and essential phase of their lives – their adulthood.
The sisters share many vital organs, including a bladder, an enlarged liver, a diaphragm, digestive systems, reproductive systems, and intestines. Each twin controls one arm and one leg that requires a lot of cooperation to complete their day-to-day tasks like running, walking, or driving a car. They were found saying that their body has been divided by a red line. One controls the left, and the other controls the right. They need to work together to be able to move properly.
The First TV Appearance
The world first saw Abby and Brittany in 1996, when the renowned celebrity, Oprah Winfrey invited them to her show. The little girls talked about their school life and shared other details of their daily routine.
They were also seen in several documentaries – Joined for Life, Extraordinary People: Twins Who Share a Body, and Abby and Brittany: Living in One Body, to name a few. Both the females used the medium of these documentaries to talk about their daily lives and how they learn to live fulfilling lives having different interests and passions. Abby loves solving math, while Brittany is a born writer and is often seen penning down notes in her diary.
From Twins to Famous Celebrity Twins
The twins lived their early life unnoticed by many. It was only a few articles and news segments that highlighted their condition and made this medical condition the topic of discussion. It was during their teen life that both the girls became famous. Many people looked forward to knowing about them in detail.
After the success of that one episode on the Oprah Winfrey Show and several television documentaries, the twin sister made a big announcement. They introduced their own reality show, Abby and Brittany, on TLC. The 8-episode show aired in 2012 and earned the twins a great fan base. So many people continued to love and admire the liveliness of both the sisters. The series documented the life events of both the sisters, like graduating their college, traveling to Europe, and finding their first job. Unfortunately, the show didn’t last long and went off-air.
Where are the Hensel Sisters Now?
In many ways, the conjoined twins were seen enjoying a perfectly normal life. They attended school, graduated college, and were highly social. They have a supportive family and friends. Managing everyday life together and overcoming the challenges that it throws is not a problem anymore for them. They even passed their driver’s license test together and played sports during their college days.
As of now, the 31-year-olds live a quiet life in their hometown. It was reported that they work as teachers at a school.
Their school principal was quoted saying both Abby and Brittany are a great source of inspiration to young children. Before they secured jobs as teachers, the supervisor of the school asked their students to react honestly to the pair. The students reportedly said that both the teachers are a part of their classroom.
The supervisor also mentioned that both the sisters offer a unique learning experience to the students, something that the other teachers in the school cannot provide. According to him, “There’s no question in my mind that they will really change the world for the better and influence lives in ways that those lives myself as one person never really do.”
The school principal employed the sisters because of their qualifications and ability to inspire the students to work hard to fulfill their dreams. According to him, “I don’t think there’s anything that they won’t try or something that they couldn’t be able to do if they really wanted to. To bring that to children, especially kid who might be struggling, that’s very special, that’s learned through lived example”.
In general, the twins have been pretty open and vocal about their trials and tribulations in front of the media. However, there is one thing at which they prefer sealing their lips. According to them, their love life is private and their privacy should be respected by the media.
Abby and Brittany are real rock stars who have proved that no matter how hard life is, there’s always a way out. Their story is inspiring for one and all. We wish them the best life ahead.
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.
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