Mom straps baby in carseat and tosses her out second-story window just seconds before taking her final breaths. Full story in the comments 

Nothing really beats mother’s love, don’t you think so? When a woman gives birth, her whole life changes and all that matters is the well-being of her bundle of joy. There is literally nothing a mom wouldn’t do for her child, and this sad and heartwarming story is just another proof of that.

Shelby Ann Carter, a 21-year-old woman from Wyoming, Ill, gave birth to a beautiful baby girl in January 2017. She and her boyfriend couldn’t be happier with the new addition to their family. Things just felt perfect for these new parents.

But you know what they say. Things don’t always turn out the way we want and expect. Sadly, the life of this loving family turned upside down as a result of a devastating tragedy.

On January 30, the mom and her baby were staying at Shelby’s mother’s house where they lived when suddenly the place caught fire.

The flames were spreading so quickly that the whole house got filled with heavy smoke and there was no way out.

Firefighters came at the scene as quickly as they could and did all in their power to put the flames under control, but unfortunately, it was already way too late for Shelby to be saved. She died due to carbon monoxide poisoning.

In the midst of the panic, Shelby tried to save her baby girl and everyone was left stunned when they realized what this mother did before she lost her life.

Firefighters came at the scene as quickly as they could and did all in their power to put the flames under control, but unfortunately, it was already way too late for Shelby to be saved. She died due to carbon monoxide poisoning.

In the midst of the panic, Shelby tried to save her baby girl and everyone was left stunned when they realized what this mother did before she lost her life.

Once she realized it was impossible for them to get out of the house, Shelby put the baby into the carseat, made sure she was secured with the belts, and then dropped her from the second-floor window. This woman didn’t care for her own life as long as her daughter would survive. This is sort of sacrifice only a mother can make.

The moment the firefighters spotted the little soul, they rushed her to the hospital, praying she didn’t suffer any serious injuries from the fall. Luckily, baby Keana was completely unscathed thanks to her mommy’s love and quick-thinking.

“It’s just incredible that she was able to pull her thoughts together to save her baby… I’d say it’s nothing short of a miracle the way it ended up”, Chief of the Wyoming-Speer Fire Protection District Ed Foglesonger told The Washington Post.

The loss of the young mother was a real tragedy that left the residents of Wyoming grieving. A baby was left without her mommy, and a family was broken forever.

Members of the community gathered to express their condolences and were willing to help Shelby’s family rebuild their house. After the word about the tragic and heartbreaking event spread, kind-hearted people helped raise almost $40,000 in just a few weeks.

We are deeply sorry for the loss and we feel sad Keana will never get the chance to meet her heroic mother who saved her life.

Once she realized it was impossible for them to get out of the house, Shelby put the baby into the carseat, made sure she was secured with the belts, and then dropped her from the second-floor window. This woman didn’t care for her own life as long as her daughter would survive. This is sort of sacrifice only a mother can make.

The moment the firefighters spotted the little soul, they rushed her to the hospital, praying she didn’t suffer any serious injuries from the fall. Luckily, baby Keana was completely unscathed thanks to her mommy’s love and quick-thinking.

“It’s just incredible that she was able to pull her thoughts together to save her baby… I’d say it’s nothing short of a miracle the way it ended up”, Chief of the Wyoming-Speer Fire Protection District Ed Foglesonger told The Washington Post.

The loss of the young mother was a real tragedy that left the residents of Wyoming grieving. A baby was left without her mommy, and a family was broken forever.

Members of the community gathered to express their condolences and were willing to help Shelby’s family rebuild their house. After the word about the tragic and heartbreaking event spread, kind-hearted people helped raise almost $40,000 in just a few weeks.

We are deeply sorry for the loss and we feel sad Keana will never get the chance to meet her heroic mother who saved her life.

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.

Related Posts

Be the first to comment

Leave a Reply

Your email address will not be published.


*