The 2024 election is on the horizon, and it appears former President Donald Trump has all but Iocked up the Republican side of the contest.
Despite, or perhaps because of, the continued efforts from the left, Trump’s popularity and poll numbers have spiked, particularly with minorities, which is terribIe news for Democrats.
Joe Biden is the incumbent, but he is getting a challenge from Robert Kennedy Jr. as a third-party candidate, and there are rampant rumors about Biden getting replaced on the 2024 Democrat ticket. Biden’s age and declining mentaI state are clearly an issue, but the Democrats also do not have a particularly deep bench in terms of potential replacements.
There have been rumors of California Governor Gavin Nesom prepping to run, as well as Vice President Kamala Harris, but both are widely regarded as failures and barring an unexpected bid from the likes of Michelle Obama, the left has precious little to offer.
This leaves us with a likely Biden/Trump slugfest in 2024. Sensing a Democrat worst-case scenario, namely, President Trump getting another term, some Hollywood celebrities have aIready begun talking about leaving the country should Trump run it back in 2024.
It should be recalled that numerous Hollywood liberals vowed to leave the country in 2016 should Trump win. Predictably, exactly none of them did, but that doesn’t mean the usual suspects won’t be threatening the same in 2024.
Recently, Barbara Streisand made some well-worn promises to leave the country should Trump win. Promises, promises.
In an interview promoting her one-thousand-page autobiography, Streisand said this: I will move. I can’t live in this country if he became president.”
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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