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

A Crucial Step: Establishing Guardianship for Adults with Special Needs

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Did 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

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Look 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

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Polly 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!

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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

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Click 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.

Decoding the Autism Trust: Non-Profit or Personal Profit?

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I’ve taken a deep dive into the workings of the Autism Trust, and I’ve found that all you need to do is a quick Google search to uncover a wealth of information about this non-profit organization. Despite the ease of access to this data, I’ve noticed a troubling indifference among the public. It seems that people are becoming desensitized or worn down to a point of apathy. But not me – I’m determined to seek out the truth and share what I discover, a quality that feels increasingly rare these days.

During my investigation, I stumbled upon the Trust’s 2019 filings and noticed hefty donations coming in from various sources, including the relentless fundraising campaigns involving the VAX bus. The Autism Trust has received millions, with figures like Del Big Tree contributing to these large sums. It’s a lot to take in, and I encourage you to follow this story closely. However, something doesn’t sit right with me about how these funds are being used, especially when considering the Trust’s zoning disputes and the muted progress on their ambitious plans for providing services to individuals with autism.

My skepticism only grows as I reflect on the Trust’s trajectory and the mysterious quiet surrounding their current operations. A generous 40-acre land donation by Bertha Bradley, intended to support people with autism, raises more questions than answers about the Trust’s effectiveness. With my background, having a family deeply involved in non-profit retirement communities, I understand the complexities and potential for secretive financial setups. And looking ahead, I am concerned about what will become of the individuals with autism as they and their caregivers grow older. My family has been fortunate to secure good care for our child, but my heart goes out to those still searching for solutions. I urge everyone to stay curious, to keep asking questions, and to demand transparency for the sake of all the families facing these challenging circumstances. May they find the support and solutions they so desperately need.

Driving Down Memory Lane with Weston Going to School

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Audiobook:
Light in the Darkness: My Search for Meaning

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Light in the Darkness” delves into the deeply personal and tumultuous journey of a man who discovers his true parentage, entangled in the dark history of eugenics. As he unravels the painful truth of his origins, he finds himself confronting a haunting legacy that extends beyond his own identity. The narrative takes a poignant turn as his children are unexpectedly plunged into the depths of autism, a mysterious connection woven through the threads of eugenics. Despite the obstacles and the donor’s refusal to provide closure, the protagonist embarks on a quest to piece together the fragmented fragments of his past, driven by a relentless pursuit for answers and healing. Throughout this gripping tale, themes of resilience, love, and the power of understanding intertwine, leading to a profound revelation that promises the possibility of finding wholeness amidst shattered reflections.

Length: 4:14:47
File size: 117MB

Click the button below to save the MP3 audio file to your favorite on-the-go player.

Buy the physical book on Amazon here!

From Adoption Dreams to Vaccine Nightmares:
The Story of My Son Weston – Part 1

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I often ponder how this entire ordeal began. As I reminisce, I remember the excitement and anticipation my wife and I felt when we decided to start a family after our marriage. Despite the challenges of in vitro fertilization and the costly efforts, our dreams were shattered when it didn’t work. We then embarked on an adoption journey, only to discover the long wait times due to a high demand for adoption. Nonetheless, our determination led us to being chosen by birth parents, Cassandra and Alex, who were young but wonderful individuals. We closely followed Cassandra’s pregnancy, eagerly awaiting the birth of our son, Weston.

Weston was a bundle of joy, but as the months went by, he began to exhibit health concerns. After every doctor’s visit and vaccination, his health deteriorated. It was heartbreaking to see our once vibrant child become so unwell, especially when doctors kept dismissing it as normal childhood illnesses. The turning point was the MMR vaccine, which dramatically changed Weston’s life and consequently ours. We couldn’t fathom how such a trusted medical procedure could have such dire consequences.

The impact of Weston’s vaccine injury propelled me into a mission to understand more. In my business, I began to interact with other parents, gathering stories and finding a pattern. The more I delved into the topic, the more enlightened I became about the realities and deceptions surrounding vaccinations. Today, as I witness the daily struggles of my children, Weston and Emily, I am reminded of the immense responsibility and challenge of parenthood. Despite the hardships, their presence is a precious gift, and I strive every day to give them the best life possible.

Copyright © 2025 by Greg Wyatt