It appears to be an innocuous picture of a mother nursing her child at first glance. But if you look closely, you can see the little element that made this photo go viral.
The act of breastfeeding is a wonderful and natural way for a mother and her little one to bond and build intimacy.
Moms shouldn’t feel guilty about feeding their children whenever and wherever they are hungry, but regrettably, some people criticize them because they think it’s improper or unacceptable for them to feed their children in public if they don’t use a cover.In 2018, while dining at a restaurant with her family and friends, Melanie Dudley, a mother of a 3-month-old child, noticed the infant wailing for food. Melanie, originally from Texas, immediately began nursing her son. And while that was great with everyone, it appeared that the stranger seated at the adjacent table was uncomfortable with the mother’s lack of coverage while nursing.
Melanie was contacted by him and requested to hide. She did just that, though not in the way that the stranger had anticipated.”I was asked to cover myself by a man while on vacation in Cabo San Lucas with my whole family. We were sitting at the rear of the restaurant, but I’m generally discrete,” Melanie said to Yahoo.It was really hot, even though I was wearing a cover. The Texan told TODAY, “It was about 95 degrees, and my little baby was sweating.””I said, ‘What do you know?
I’m taking this off; I’m on vacation.
The entire restaurant burst out laughing when Melanie took the cover off and wore it on her head.I simply placed it above my head. I’m not sure why. It wasn’t even close to being a scandalous altercation. That was all I had to say. I was at a loss for words, so I decided to just hide my head,” the woman said.Carol Lockwood, a witness to the entire event, snapped a picture of Melanie and posted it online with the remark, “I’ve never met her, but I think she’s AWESOME!!!”Kindly distribute! I have made this content public with permission. I’m so sick of hearing people shame women for nursing! The picture was shared 225,000 times and counting in no time at all.
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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