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The Tightrope of Cognitive Dissonance
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DEL BIGTREE’S MESSAGE: A FEARFUL SERENADE
Cognitive dissonance often arises in the messaging of Del Bigtree. He wields the power of persuasion with charismatic authority, all without the credentials of a medical professional. His message is clear but contentious: vaccines can be safer, and there are hidden dangers within the medical establishment.
It is difficult to argue the latter; there are hidden dangers within the medical establishment, but there is no clear path to safer vaccines.
Del’s narratives resonate with those who question the status quo. His skillful blend of partial truths and fear-mongering serves as an unsettling serenade. He plays the notes of doubt, painting a grim picture of vaccines as a looming threat.
This melody resonates with the anti-vaccine and vaccine-hesitant, sowing the seeds of discord within their minds. The danger is that he sets himself as an authority on the subject, and so many people flock to him that if he said, “This is the vaccine to trust,” his followers would run out and get it.
DECEPTION IN THE ECHO CHAMBER
Del Bigtree’s unique deception lies in his ability to exploit this cognitive dissonance. He deftly caters to his audience’s fears and doubts while offering himself as a beacon of clarity in the fog of uncertainty. His messages shift with the crowd’s desires, mirroring their beliefs while maintaining an authoritative facade.
He portrays himself as a truth-teller, a champion of safer vaccines, even when the Supreme Court acknowledges vaccines as “unavoidably unsafe.” This intentional manipulation amplifies cognitive dissonance as his followers grapple with his ever-evolving narrative.
A Crucial Step: Establishing Guardianship for Adults with Special Needs
/0 CommentsDid you know?
When a child with special needs reaches the age of 18, they are legally recognized as an adult in most U.S. states, a transition that can have significant legal implications, especially for those receiving state benefits. This change means that these individuals now have the right to make their own decisions regarding healthcare, finances, and personal affairs. For parents and caregivers, this often necessitates a legal shift in responsibility. To continue making crucial decisions for their child who may not be fully capable of managing their own affairs due to their disability, they need to petition the courts for guardianship. This process, varying in its specifics from state to state, requires demonstrating to a court that the adult child is unable to independently manage their affairs. Guardianship can be full, encompassing all aspects of the individual’s life, or limited to certain areas such as financial or healthcare decisions. Given the profound impact on the rights and autonomy of the individual with disabilities, this decision requires careful consideration, and often, the guidance of legal counsel. Exploring all options, including supported decision-making models, is crucial in ensuring the continued wellbeing and support for these new adults, aligning legal responsibility with their best interests and unique needs.
Weston Home for Thanksgiving
/0 CommentsLook who’s back! We are so blessed to have our boy come visit for the Thanksgiving holiday! There is nothing that brings us more joy than for our family to be reunited!
The Autism Trust
/0 CommentsPolly Tommey and her husband, Jonathan Tommey, ripped off the parents by giving false hope about where their kids would go when they were no longer around. It was a brilliant move of marketing and exploitation and fit in perfectly with their new black bus movie that trauma bonded the masses by lies and deception and promises of turning the 1986 act over. If that one solitary thing had happened we would not be in this hell hole of the situation. And now we’ve got RFK Polly’s boss leading the vaccine-injured parents. He says he’s not anti-vaccine, but then when you ask his followers they give you a different story. He wants to make them safer. Rinse wash, repeat, rinse, wash, repeat. Doesn’t anyone get it except me?
Polly formed the Autism Trust in Austin Texas for these exact situations. Once a job opening came working with RFK she abandoned it and moved on to her next grift. Her son Billy and Ken whose mother gave them the land and ongoing tens of thousands of dollars a month for its operations only have these two people living there outside of their friends. What a lonely sad way to live Polly! You know what you’ve done!
In this video, recorded on December 30, 2021, I delve into the controversial figure of Andrew Wakefield and his involvement in the vaccine safety movement. I accuse Wakefield, along with others like Barbara Lowe Fisher and Del Bigtree, of exploiting public fears for their own gain, labeling them as “monetizers of misery” within a dubious syndicate. I highlight Wakefield’s transition from a medical professional to a full-time filmmaker, particularly criticizing his film “1986: The Act” as misleading and ineffective.
My primary argument centers on the deceptive nature of the ‘safer vaccines’ campaign, which I believe is a tactic used by Wakefield and his associates to profit through films, charities, and nonprofits, under the pretense of advocating for public health. I draw on personal experiences, especially my struggles related to the 1986 Vaccine Injury Act and my son Weston’s case, to illustrate the lack of evidence supporting Wakefield’s claims.
Furthermore, I discuss Wakefield’s patent application for a new vaccine, which I see as contradictory to his public stance on vaccine safety. I question the existence of ‘safer vaccines’ and criticize the lucrative careers built by individuals like Wakefield at the cost of public trust. The video concludes with a reflection on the personal impact these issues have had on my family, especially my son Weston, and emphasizes the need for truth and skepticism in the vaccine debate.
An Autistic Teen Needed Mental Health, But Spent Weeks in the ER Instead
/0 CommentsClick HERE to read the complete article.
The article details the harrowing experience of Zachary Chafos, an autistic teenager, and his family as they faced prolonged waits in an emergency room for psychiatric treatment. In November 2020, amid a severe mental crisis exacerbated by the pandemic, Zachary was taken to Howard County General Hospital. However, due to a shortage of psychiatric beds in Maryland, he and his parents endured an agonizing wait in the ER, where Zachary’s condition worsened. The article highlights the broader issue of psychiatric bed shortages in the United States, particularly in Maryland, which has some of the longest ER wait times for psychiatric treatment. This problem has been exacerbated by the pandemic, with a significant rise in young patients needing psychiatric care. Despite efforts and promises from Maryland officials over the past decade, the situation has only deteriorated, especially for children and teenagers. The article also touches on the challenges and frustrations faced by the healthcare system and families in finding timely psychiatric care, exacerbated by systemic issues like insurance denials, low reimbursement rates for providers, and shortages of mental health professionals. The story of Zachary Chafos is a poignant example of the dire consequences of these systemic failures.
Click on the above image to watch a video where I share some important thoughts that drive me… especially 666, Mark of the Beast.
Greg Wyatt