Note: we are republishing this story to raise awareness for the Mike Biadasz farm safety and education memorial fund. Learn more at their Facebook page here as well as their website here.
A farmer and 16 of his cattle have died in a freak accident after a “dеаdly dome of air” formed in a Wisconsin farm’s manure holding tank.!!
According to WAOW, a 29-year-old farmer named Michael Biadasz, from Amherst, Wisconsin, died of gas poisoning on his family’s farm after being overcome by fumes of either methane or sulfur oxide. Initially, 13 of the farm’s cattle died as well; later, three more expired, bringing the total to 16 cattle dеаths.
The 29-year-old’s father, Bob Biadasz, co-owner of Biadasz Farms, said that the tragedy was the result of a “perfect storm” of unusual and unexpected weather conditions. When the tank was prepped to be pumped, warm upper air temperatures trapped the gases in a dome of air which then poisoned Michael and the cattle.
Biadasz was reportedly found dеаd when other workers arrived to begin hauling manure away from the tank.
“The family is devastated, absolutely devastated,” Portage County Coroner Scott Rifleman told WAOW.
Rifleman told WSAW that gas poisoning dеаths typically occur in closed areas, making the incident even more surprising. The coroner said that atmospheric pressure prevented the gases from dissipating.
The coroner went on to say that an investigation is underway to determine exactly what caused Biadasz’s dеаth. According to Rifleman, Biadasz had safely emptied the same tank hundreds of times prior to the fatal incident.
The Biadasz family honored Michael by parking a line of tractors and machinery along the road that passes the farm. Among the vehicles parked are a blue tractor, several red trucks, and Michael’s black pickup truck…
“As if there isn’t already enough dаngеr in the lives of farmers, this family had to suffer this freak accident,” one Facebook user commented on the story. “So sad.”
Following the tragic accident, many are calling for tougher regulations to be placed on manure holding tanks to prevent a similar incident in the future. According to All That’s News, the National Agriculture Safety Database says that there should be proper ventilation in areas where animals are stored and that warning signs must be posted nearby.
“In addition to adhering to proper construction and maintenance procedures for liquid manure storage facilities, owners should be encouraged to follow a few precautionary measures to protect both workers and livestock from harmful manure gases,” the NASD writes.
WASW reports that a similar unfortunate fate befell a Virginia family in 2007, when five of its members died as a result of a pipe blockage that caused a fatal buildup of methane gas.
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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