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Climate Trails Documentary

https://climatetrails.com/  Trailer Here

CLIMATE TRAILS

4K UHD72-hour rental
In a world where the skies are no longer trusted, Climate Trails uncovers one of the most urgent issues of our time, geoengineering and the phenomenon known as “chemtrails.”

Featuring a military whistleblower, a biologist, a doctor, environmental activists, and everyday citizens, it exposes hidden agendas shaping the skies above us. With growing evidence of strange cloud formations and unexplained illnesses, they embark on a quest to expose the truth behind what’s being sprayed above our heads.

From the mountains of Mt. Shasta to the plains of Texas, Climate Trails takes viewers on a journey across polluted skies and waking minds. It’s not just a documentary, it’s a call to awareness, a warning, and a demand for transparency in a world where the air we breathe is no longer our own.

Watch on your phone, tablet, computer, or beam to your TV via AirPlay/Chromecast using the Vimeo player above. Rental unlock lasts 72 hours once started.

For more:

Lastly, but certainly not least is the finding of spider silk proteins (polyamides) developed and deployed since 2002 by a company focused on the development of biodefense therapeutics.

These proteins are the same proteins found in the rubbery, white clots in people who got the covid gene therapy shots: https://madisonarealymesupportgroup.com/2024/01/17/spider-webs-in-the-pfizer-closet-silk-polymer-geoengineering-link-to-morgellons/   We are inhaling these polymers and they are replicating in our bodies. 

All of this could very well explain Morgellons – a Lyme-like illness with colorful fibers coming out of the skin that an independent researcher has connected to the deliberate introduction of massive amounts of particulates into our atmosphere called chemtrails.

When Lyme Stopped My Childhood

https://magazine.publichealth.jhu.edu/2025/when-lyme-stopped-my-childhood

When Lyme Stopped My Childhood

The tickborne disease stole years of my life, but it also revealed my superpower.
By Kristen Johansson
10/10/25

I was 11 when my body changed. First came the fevers and headaches. Then tremors. Then seizures.  

Joint pain and frequent injuries meant sports disappeared. Brain fog and panic attacks meant school did too. By eighth grade in 2019, I was absent from most everything that had once defined me. I went from being a straight-A, four-sport student with a thriving social life to spending Thanksgiving and Christmas in the hospital. 

After two and a half years of severe illness, 30 doctors, and multiple misdiagnoses, I finally had an answer in 2020: Lyme disease, bartonellosis, and babesiosis. The diagnoses of three tickborne diseases brought some hope, but names alone couldn’t bring relief. My immune system was so depleted that a bout of mononucleosis that year broke me. 

I lost the ability to read. To walk. To talk. To eat. Even my short-term memory failed. My body stopped producing blood, making testing impossible. The hospital sent me home and told my family to prepare for me to die. 

But immunotherapy and aggressive treatment with long-term antibiotics, countless supplements, and daily injections gave me back pieces of myself. The first time I could read again, I clutched the words like they were oxygen. 

More than novels or school assignments, it was research that became my anchor. I became a detective, immersing myself in a cold case file of my old lab results and new studies, searching for answers that puzzled even my doctors. My days blurred into hours of YouTube lectures and Q&As from experts—each lesson a clue helping me to decipher how an infection could ripple through so many parts of me. When my liver could no longer withstand the harsh drugs I’d been taking for years, I researched alternatives, drawing on pioneering studies by Johns Hopkins researchers. I brought printed copies of these articles on herbal therapies to my doctors, ultimately shaping the protocols that led me to remission. (See link for article)

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**Comment**

Completely relatable.

Similar stories only the names have been changed….

For more:

Health Officials Issue Warning As Lyme Disease Reaches ‘Endemic Levels’ in West Virginia

https://www.yahoo.com/news/articles/health-officials-issue-warning-dangerous

Health officials issue warning as dangerous disease reaches ‘endemic levels’: ‘It’s not if you’re going to get it, it’s when’

Katie Dupere

A region in West Virginia is experiencing “endemic levels” of Lyme disease. It’s a clear example of how warming global temperatures are transforming some regions into breeding grounds for diseases.

What’s happening?

Ohio County — which has a population of about 40,000 — is experiencing an alarming number of Lyme disease cases. As of mid-September, there were almost 300 reported cases. Health officials warn the illness is now so widespread that cases are no longer investigated but simply recorded.

“It’s not if you’re going to get it, it’s when you’re going to get it,” Wheeling-Ohio County Health Department Administrator Howard Gamble told local news affiliate WTOV 9.

Lyme disease is a bacterial infection transmitted to humans through the bite of infected ticks. It can cause fever, fatigue, joint pain, and a characteristic “bull’s-eye” rash. If left untreated, Lyme may lead to serious complications affecting the heart, joints, and nervous system.

Ohio County officials attribute the surge to unstable environmental conditions and human proximity to animal habitats that support tick populations. And those factors can be directly tied to rising global temperatures.

Spring and summer are peak tick seasons — but health officials warn cases are not expected to decrease significantly in the fall.  (See link for article)

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**Comment**

Sadly, another article pushing the ‘climate change’ agenda which has been proven by independent research to be a mute point regarding ticks and disease proliferation, yet a lie is halfway around the world before the truth is still putting on its shoes.

Further, these articles never manage to even mention the fact our own government has experimented upon ticks for decades, purposely infecting them and then dropping them out of airplanes…..

For more:

Bioengineering Without Boundaries: Why Lyme Disease Belongs in the GMO Debacle

https://gmoscience.org/2025/10/20/bioengineering-without-boundaries-why-lyme-disease-belongs-in-the-gmo-debacle/

Bioengineering Without Boundaries: Why Lyme Disease Belongs in the GMO Debacle

Michelle Perro, MD
Published: October 20, 2025

Lyme disease is not simply an infection.  It is a lens into the consequences of manipulating biology without accountability. As we confront the obfuscated crisis of Lyme and other chronic infections, it becomes evident that bioengineering in pathogens and genetic engineering in food are part of the same continuum of unregulated biotechnology. Both alter life’s blueprints, both evade oversight, and both are creating a legacy of ecological and human suffering.

In her groundbreaking book, Bitten: The Secret History of Lyme Disease and Biological Weapons, science journalist Kris Newby details how US biowarfare research programs, including work at the Rocky Mountain Laboratories in Hamilton, Montana, experimented with spirochetes to alter virulence and transmission. The intention of these manipulations, although unclear, likely spawned Borrelia burgdorferi, the stealth pathogen now linked to millions of chronic infections worldwide. The same recombinant DNA methods used in agricultural GMOs were being applied in microbial genetics at the time.

“When we manipulate genes for profit or power, the consequences ripple through ecosystems, our children, and future generations.”

Lyme rarely acts alone. It often coexists with Bartonella, Babesia, EhrlichiaMycoplasmaRickettsiae, and viruses such as Powassan, all of which exacerbate inflammation and neuroimmune dysfunction. These infections disrupt the immune system through biofilm formation, cytokine storms, and molecular mimicry, while simultaneously impairing gut barrier integrity; a condition known as ‘leaky gut.’ This state of immune chaos parallels the chronic inflammation seen in individuals exposed to genetically engineered foods and glyphosate residues.

Despite their shared roots in biotechnology, genetically modified foods and engineered pathogens are regulated separately by the USDA, EPA, FDA, NIH, and DOD, none of which coordinate holistic biosafety. This fragmented oversight allows both agricultural and biomedical engineering to advance without unified accountability. The same regulatory capture that shields agri-tech corporations has also protected infectious disease gatekeepers, such as the Infectious Disease Society of America (IDSA), whose restrictive guidelines have left millions of chronic Lyme patients untreated.

Just as the FDA dismisses independent research on GMO toxicity, the IDSA dismisses clinicians and patients suffering from persistent Lyme. Both systems denied chronic exposure or chronic infection, labelled dissenting experts as “fringe,” protecting corporate and institutional interests over public health.  The pattern created is systemic and taken directly from the GMO playbook: create complexity, deny chronicity, and suppress those questioning the government/corporate narrative.

Lyme Mythology

Lyme Disease is the modern plague that never shouldn’t have been. It is now one of the fastest-growing infectious diseases in the United States, with the CDC estimating up to 3 million cases annually when underreporting is considered.

Although black-legged ticks (Ixodes scapularis and I. pacificus) are the best-known carriers, Borrelia DNA has been detected in a variety of other insects, suggesting other forms of transmission.  This fact is little known in mainstream medicine and leaves those with Lyme disease unclear as to how they were infected when consulting with their physicians who just believe that the tick is the only vector of Lyme.

The Multi-Vector Reality: Beyond the Tick

The following graph demonstrates that there are many other potential vectors of Lyme disease which should increase our awareness when facing those with multi- system complaints and health challenges.

Insect Evidence of BorreliaDNA Proven Transmission to Humans Comments
Ticks (Ixodes scapularisI. pacificus) Strong Yes Primary vector
Mosquitoes (AedesCulex) Moderate No Possible mechanical transmission
Horseflies / Deer flies Moderate No Possible mechanical role
Fleas  Detected No Reservoir role in pets/rodents
Mites Rare No Wildlife vector potential
Lice (Pediculus humanus) Different Borrelia) Yes (B. recurrentis, relapsing fever) Demonstrates Borrelia versatility

Sources: Schotthoefer & Frost, 2015; Franke et al., 2020; Eisen et al., 2017; Jaenson et al., 2019.

Integrative Framework

Healing requires more than antibiotics or symptom management. It demands restoration of biological integrity. Integrative and terrain-based approaches rebuild the immune system through microbial, nutritional, and energetic balance.

The gut-immune axis is central to Lyme’s chronicity. Dysbiosis from antibiotics, poor diet, and/or environmental toxins (e.g., glyphosate, heavy metals) compromises the gut-associated lymphoid tissue (GALT).  Over 70% of immune function resides in the gut creating conditions where infections persist and autoimmunity originates.

Supporting terrain integrity is essential though the use of an organic regenerative diet with strict avoidance of glyphosate-contaminated foods (which destroy beneficial gut flora).  Additionally, a whole foods based diet composed of increased polyphenols, flavonoids, healthy fats, and fiber are paramount to healing.

An integrative approach is necessary when helping those with Lyme disease and treatments stem from a multimodal tool box with suggestions outlined in article (See top link).

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**Comment**

One of the best articles I’ve read in a spell.  

My only qualm is with the treatment and transmission info. The antibiotics listed are not the only ones that work and their usage presented is not savvy enough.  Please see:   https://madisonarealymesupportgroup.com/2016/02/13/lyme-disease-treatment/

Lyme literate doctors (LLMDs) have learned to track symptoms and then use treatment that works on given symptoms (that change).  This requires different drugs.  Also, once you beat back Lyme enough, it is quite normal for coinfections to become evident.  These also require different drugs.  Further, dosage matters.  Then, there’s the issue of pulsing and cycling – both techniques that experienced LLMDs use – precisely due to needing a judicious approach since treatment is often protracted.  Throwing antibiotics at this indiscriminately is unwise.

Treatment must be fluid to adapt to the ever changing symptoms.

Also, besides congenital transmission, sexual transmission is highly likely:

The Spike Protein and the Spirochete: SARS-CoV-2 Infections, Reinfections and Exposures to its Spike Protein May Effectively Simulate “Lyme Disease”

https://wmcresearch.substack.com/p/the-spike-protein-and-the-spirochete?

Just like the Lyme Disease pathogen, the Spike Protein invades organs through – the endothelium – with remarkably similar results.

Dependence of B. burgdorferi–endothelial interactions under physiological shear stress on pFn. (A) Schematic illustrating initiation steps (tethering, dragging) of the B. burgdorferi–endothelial interaction cascade leading to bacterial transmigration across endothelial barriers into extravascular tissues. Tethering bacteria anchor to endothelial surfaces via tethers, pause repeatedly as they move over endothelial surfaces, but move faster than 100 μm⋅s−1. Dragging bacteria move more slowly (<100 μm⋅s−1) and are untethered. Both tethering and dragging are Fn-dependent in mouse PCVs (18). There are reduced numbers of B. burgdorferi tethering and dragging on primary human endothelial monolayers in flow chambers at typical PCV shear stress (1 dyn/cm2) following treatment with polyclonal anti-Fn antiserum (B) and depletion of pFn from serum in bacterial cultivation medium (C). Numbers of tethering and dragging GFP-expressing B. burgdorferi (strain GCB966) in the presence of nonspecific IgGs or polyclonal αFn IgGs were measured by manual counting. In B, GCB966 was cultivated in the presence of mouse blood before imaging. In C, bacteria were cultivated without mouse blood to eliminate all sources of pFn. In C, −pFn indicates pFn-depleted growth conditions; for +pFn samples, bacteria grown under pFn-depleted conditions were supplemented with human pFn (+pFn) to the concentration present in blood (0.3 mg/mL) before imaging. Summary values: mean ± SEM. Statistics: two-way ANOVA, Holm–Sidak posttest (n = 3 independent bacterial and endothelial cultures per group). *P < 0.05 vs. IgG (B) or −pFn (C) within the same interaction type.

We can learn much about the Spike Protein by studying Lyme Disease. It is remarkable how much commonality Spike Protein-related disease and Lyme Disease share. Let’s start with infection. For Lyme Disease, it is through a tick bite. For the Spike Protein, it is through the respiratory tract (directly into the bloodstream, too, unfortunately). For example, we can edit Lyme Disease pathogenesis to mirror the Spike Protein’s.  (See link for article)

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**Comment**

This is the first time I’ve seen Lyme compared to the spike protein; however, when you study how both disseminate in the body, there are similarities – not to mention how ‘the powers that be’ have treated both diseases (censorship, denial of effective treatment, the push for a ‘vaccine,’ etc.)

Just today, a study came out stating:

Our findings reveal that the first contact of B. burgdorferi and blood vessels is not random but involves close interactions with pericytes. We also capture the infiltration of immune cells in the skin and their interactions with invading bacteria. Altogether, these observations suggest that Borrelia strategically targets vascular regions with lower mechanical resistance to breach the endothelial barrier, thereby enhancing its dissemination.

In other words, Bb has tricks up its sleeve.  But we always knew that.

In the Discussion section the authors admit:

Due to the wave-like morphology and typically low abundance of pathogenic spirochetes in tissues, it is challenging to accurately identify the bacteria from random 2D electron microscopy projections. To reliably confirm the presence of Bb, one must either employ a correlative approach35 or conduct a complete 3D reconstruction of the spirochete.

And herein lies the problem: researchers are not using advanced enough techniques to find these elusive organisms causing so much damage.

The authors also state they found Bb in collagen bundles which provide natural pathways for migration through connective tissue which then gets degraded in later disease stages, but that by:

avoiding overt destruction of host tissues, Bb may reduce the likelihood of triggering host defense mechanisms that could thwart its spread.

So, no, you are not going nuts.
You are infected with a sneaky organism with an affinity for skin, bones, tissues, and tendons and yes, you will painfully feel it. 

Further, the study demonstrates a sort of intelligence to Bb:

The initial phase likely represents a “probing” stage during which the bacteria survey the microenvironment. At this stage, Bb interacts with the vasculature using a smaller area of its cell body, without penetrating either the PCs, ECs, or the surrounding BM (Fig. 2). This is followed by a second phase characterized by a gradual increase in the number of endothelial contact sites, suggesting a transition from transient adhesion to a more stable interaction prior to traversal.

You can read my comments to the top article by going to the top link.