Ditch These Foods to Heal Chronic Illness
Explore the hidden biochemical triggers of inflammation and the foods that stoke the flames,
Perfect for those battling autoimmune diseases, neuroinflammation, chronic fatigue, IBD, MS, arthritis, or post-viral syndromes taking control of these triggers is your key to reclaiming vitality!
🌾 Gluten Sensitivity: The Hidden Inflammation Trigger
Struggling with chronic inflammation, autoimmune flares, fatigue, or brain fog?
Gluten may be silently sabotaging your gut and immune system even if you don’t have celiac disease.
🔓 Leaky Gut & Systemic Inflammation
Gluten stimulates zonulin, a protein that opens tight junctions in your intestinal lining. This leads to leaky gut, allowing bacteria, food particles, and toxins to escape into your bloodstream triggering chronic immune activation and inflammation throughout the body.
🧬 Autoimmune Activation via Molecular Mimicry
In genetically predisposed individuals (e.g., HLA-DQ2/DQ8), gluten peptides can resemble human tissue proteins. This "molecular mimicry" may cause the immune system to mistake your own cells for invaders, contributing to diseases like:
• Hashimoto’s thyroiditis
• Multiple sclerosis (MS)
• Rheumatoid arthritis
• Celiac disease
Non-Celiac Gluten Sensitivity (NCGS) Is Real
Even without celiac markers, many people experience bloating, diarrhea, joint pain, fatigue, skin issues, and brain fog after gluten exposure.
This is known as NCGS and it's now recognized in medical literature as a legitimate, immune-mediated condition.
✅ What You Can Do
• Trial a gluten-free diet for 30–60 days and track your symptoms
• Get tested: Ask your provider about anti-gliadin antibodies or genetic screening
• Focus on whole, unprocessed gluten-free foods not just GF packaged substitutes
• Reassess and reintroduce (if desired) later to confirm your sensitivity
📌 Healing often begins in the gut. If gluten is a trigger, removing it could be the most powerful anti-inflammatory step you take.
Most commercial cow’s milk contains A1 casein, a protein that breaks down into beta-casomorphin-7 (BCM-7) a bioactive peptide linked to gut and brain inflammation.
Many people also lack the enzyme lactase, leading to poor lactose digestion, bloating, dysbiosis, and gut irritation.
Worse still, the immune system can develop IgG or IgA antibodies to casein, triggering systemic inflammation and potentially worsening autoimmune and neuroimmune conditions.
🚩 Who Should Be Cautious?
If you have any of the following, A1 dairy might aggravate your symptoms:
• Multiple Sclerosis (MS)
• Parkinson’s disease
• Chronic sinus issues or asthma
• Crohn’s or colitis
• Eczema, acne, or skin inflammation
• Brain fog, autism spectrum conditions, or neuroinflammation
Try removing dairy for 30–60 days and observe changes in energy, digestion, skin, and cognition.
✅ Better Options (Later On)
• A2 dairy (from A2 cows, goats, or sheep)
• Raw, fermented goat/sheep dairy (e.g. kefir)
These may be reintroduced cautiously in later phases, but all dairy is excluded initially to reduce inflammatory load.
📖 A controlled human study found that A1 milk increases GI symptoms and inflammation compared to A2 milk.
🔗 Read the study (Nutrition Journal, 2016)
Legumes contain lectins sticky, plant-derived proteins that resist digestion and can bind to the gut lining, increasing intestinal permeability and provoking immune activation.
They also contain phytates, which chelate essential minerals like zinc, calcium, and iron, blocking their absorption.
Soy is especially problematic: it’s often genetically modified, heavily sprayed with glyphosate, and loaded with phytoestrogens, which may disrupt hormonal balance and immune signaling.
Peanuts, technically legumes, are frequently contaminated with aflatoxins toxic fungal compounds linked to liver damage, immune suppression, and even cancer.
🚨 Who Should Be Cautious?
You may want to avoid legumes if you struggle with:
• Autoimmune diseases (e.g. lupus, RA, MS)
• Estrogen-sensitive conditions (endometriosis, fibroids, PCOS)
• IBS, IBD, or leaky gut
• Mineral deficiencies (low iron, zinc)
• Histamine intolerance or peanut allergies
💡 Smart Tips
• Pressure-cooking reduces some lectins, but not all anti-nutrients
• Eliminate legumes during early gut-healing or autoimmune protocols
• Reintroduce slowly (if at all) once symptoms stabilize
🍅 Nightshades: Nature’s Defense, Your Inflammation Trigger?
Examples: Tomatoes, potatoes, eggplant, bell peppers, chili
🔥 Why They’re Inflammatory (for Some)
Nightshades contain alkaloids like solanine and capsaicin, natural pesticides that defend the plant but can irritate the human body. In sensitive individuals, these compounds can:
• Disrupt the gut lining, increasing intestinal permeability (aka leaky gut)
• Activate mast cells, releasing histamine and pro-inflammatory cytokines
• Trigger neurogenic inflammation, leading to nerve pain, joint stiffness, or migraines
• Worsen autoimmune flares, especially in musculoskeletal and neuroimmune disorders
🚨 Who Should Be Cautious?
If you’re living with:
• Rheumatoid arthritis, lupus, or ankylosing spondylitis
• Multiple sclerosis (MS) or neuropathic pain
• IBD (Crohn’s, colitis) or leaky gut
• Migraines, eczema, interstitial cystitis, or chronic fatigue
…then nightshades could be silently inflaming your symptoms.
💡 What to Do
• Eliminate nightshades for 4–6 weeks
• Reintroduce one at a time, with 2–3 days in between
• Track symptoms like pain, digestion, skin, mood, and energy
You may discover that removing just one trigger food brings profound relief.
🍬 Processed Sugars & Refined Carbs: Silent Drivers of Inflammation
Examples: White sugar, high-fructose corn syrup (HFCS), pastries, white bread, soda
🔥 Why They’re Inflammatory
Refined sugars cause a rapid spike in blood glucose, which leads to insulin surges that activate inflammatory messengers like NF-kB and IL-6 key players in chronic disease.
They also feed pathogenic gut microbes (like candida and bad bacteria), disrupting your microbiome and triggering systemic inflammation.
Over time, sugar drives the formation of advanced glycation end products (AGEs) damaging compounds that impair mitochondrial function, degrade collagen, and contribute to brain fog, skin aging, and neurodegeneration.
🚨 Who Should Be Especially Cautious?
Watch your intake if you live with:
• Metabolic syndrome or insulin resistance
• Type 2 diabetes or prediabetes
• Alzheimer’s or cognitive decline
• PCOS or hormonal imbalances
• Candida overgrowth, acne, or chronic fatigue
• Mood disorders like depression or anxiety
These conditions are often exacerbated by high-glycemic, low-nutrient carbs.
💡 Smart Move
• Cut back on added sugars and refined flour
• Prioritize whole foods with fiber, healthy fats, and slow-burning carbs
• Notice how quickly energy, mood, and skin improve when sugar is removed
📊 Even small reductions in sugar can lead to big wins in inflammation, energy, and metabolic health.
These oils are ultra-processed and packed with omega-6 linoleic acid, which your body converts into arachidonic acid a precursor to inflammatory molecules like prostaglandins and leukotrienes.
When heated, seed oils oxidize rapidly, producing toxic lipid peroxides that damage:
• Cell membranes
• Mitochondria (your energy factories)
• DNA promoting aging, mutation, and inflammation
The result? A perfect storm for metabolic dysfunction, non-alcoholic fatty liver disease (NAFLD), cardiovascular problems, insulin resistance, and even brain fog.
🚨 Who Should Be Cautious?
These oils may worsen symptoms if you’re dealing with:
• Heart disease or hypertension
• Brain fog or cognitive decline
• NAFLD or high triglycerides
• Obesity, insulin resistance, or chronic fatigue
• Inflammatory skin issues (like eczema or acne)
💡 Smart Move
Replace inflammatory seed oils with stable, nourishing fats like:
• 🫒 Extra virgin olive oil
• 🥥 Coconut oil
• 🥑 Avocado oil
• 🧈 Ghee or grass-fed butter
• 🐖 Tallow or duck fat
These are richer in antioxidants, more heat-stable, and support cellular and metabolic health not sabotage it.
⚠️ Trans Fats: Hidden Hazards to Your Heart and Brain
Examples: Margarine, shortening, fast food fries, processed snacks, baked goods with partially hydrogenated oils
🔥 Why They’re Inflammatory
Trans fats are industrially created fats that disrupt cell membrane structure, impair insulin signaling, and damage mitochondria, your body’s energy producers.
They also:
• Raise LDL (“bad”) cholesterol
• Lower HDL (“good”) cholesterol
• Trigger systemic inflammation that accelerates aging and disease
• Increase risk of heart attacks, stroke, and neurodegeneration
They’ve been called the most dangerous fats in the modern diet and for good reason.
🚨 Who Should Be Especially Cautious?
Avoid trans fats completely if you’re dealing with:
• Cardiovascular disease or high cholesterol
• Insulin resistance or type 2 diabetes
• Cognitive decline, Alzheimer’s, or brain fog
• Chronic inflammation, fatigue, or autoimmune conditions
Even small amounts are harmful.
💡 Smart Move
• Read labels: Watch for "partially hydrogenated oils"
• Avoid ultra-processed foods and fast food
• Focus on whole foods and healthy fats like olive oil, ghee, or coconut oil
🛑 There is no safe level of trans fat. Eliminating them may be one of the fastest ways to protect your heart, brain, and metabolism.
Many food additives are designed to extend shelf life, enhance flavor, or improve appearance but at a cost to your health. Here’s how they silently provoke inflammation:
• Mast Cell Activation & Histamine Release
Preservatives and additives can activate mast cells, immune cells that release histamine and inflammatory cytokines. This can trigger skin rashes, gut symptoms, and respiratory issues in sensitive individuals.
• Excitotoxicity
Compounds like MSG (monosodium glutamate) and aspartame are excitotoxins they overstimulate neurons, potentially leading to brain inflammation, headaches, migraines, mood swings, and even seizure activity in susceptible people.
• Gut-Brain Axis Disruption
Preservatives like sodium benzoate and BHA/BHT can disrupt the gut microbiome, reducing bacterial diversity and promoting dysbiosis a known driver of systemic inflammation, anxiety, and cognitive dysfunction.
• Nitrites & Nitrates
Used in processed meats, these can form nitrosamines, compounds linked to cancer risk, oxidative stress, and endothelial damage (affecting heart and brain function).
🚨 Who Should Be Especially Cautious?
These compounds may aggravate symptoms in people with:
• ADHD or behavioral disorders
• Histamine intolerance or MCAS (mast cell activation syndrome)
• Asthma, eczema, or chronic allergies
• Neurodegenerative diseases (like Parkinson’s, Alzheimer’s)
• IBD, IBS, or leaky gut
💡 Smart Move
• Read labels carefully even on “healthy” foods
• Look for real, whole-food ingredients you recognize
• Choose additive-free snacks, cured meats, and drinks whenever possible
• Focus on home-cooked meals made from scratch
🧠 Your brain, immune system, and gut all respond to what you eat. Eliminating synthetic additives can bring surprising improvements in mood, energy, and inflammation.
FODMAPs are a group of short-chain carbohydrates and sugar alcohols that are poorly absorbed in the small intestine. They ferment in the colon, producing gas, bloating, and distension, especially in sensitive individuals.
FODMAP = Fermentable Oligosaccharides, Disaccharides, Monosaccharides, and Polyols
🔥 Why They Can Be Inflammatory
For people with gut vulnerabilities, FODMAPs can:
• Increase intestinal permeability (leaky gut)
• Feed dysbiotic bacteria, fueling bloating and inflammation
• Activate mast cells, releasing histamine and cytokines
• Disrupt serotonin balance, affecting mood, focus, and energy since ~90% of serotonin is made in the gut
🚨 Who Should Watch Out?
You may benefit from a low-FODMAP approach if you’re dealing with:
• IBS (Irritable Bowel Syndrome)
• SIBO (Small Intestinal Bacterial Overgrowth)
• IBD (Crohn’s, colitis)
• Histamine intolerance / Mast cell activation
• Mood swings, anxiety, or depression
• Chronic fatigue (ME/CFS)
💡 Pro Tip
FODMAPs aren’t “bad” — many are found in healthy whole foods. But for sensitive guts, temporary reduction can relieve symptoms while you:
• Heal the gut lining
• Rebalance the microbiome
• Calm immune and mast cell overactivity
Once stable, many people can reintroduce moderate FODMAPs successfully.
📋 Consider working with a practitioner to guide elimination and reintroduction phases for optimal results.
Certain foods can fuel inflammation at every level by disrupting immune regulation, damaging the gut lining, feeding harmful microbes, and impairing mitochondrial energy. For those with autoimmune diseases, neurological conditions, hormonal imbalances, or chronic fatigue, even seemingly “normal” foods may be silently sabotaging recovery.
But here’s the good news:
🌿 Removing dietary triggers even for 30–60 days can create a dramatic shift in how your body functions. Many experience:
• Reduced joint pain and bloating
• Clearer thinking and more stable mood
• Better skin, digestion, and sleep
• Renewed energy and vitality
🛠️ Take Action: Reclaim Your Health with a Root-Cause Approach
Start with a simple elimination protocol, removing common inflammatory foods and focusing on:
• Leafy greens and cruciferous vegetables
• Healthy fats (olive oil, avocado, coconut, omega-3s)
• Clean protein sources (grass-fed, pasture-raised, wild-caught)
• Gut-healing foods (bone broth, fermented veggies, herbs)
After 30–60 days, reintroduce foods one at a time, tracking how your body responds physically, mentally, and emotionally. This process helps you decode your body’s signals, rebuild resilience, and make empowered food choices for life.
🧠 Your diet isn’t just fuel it’s information. Removing inflammatory inputs allows your body’s innate intelligence to reset, repair, and thrive.
#metaanalysis #ExcessDeaths
#NL #Netherlands 🇳🇱🇳🇱🇳🇱🇳🇱
The research report examines a potential relationship between COVID-19 vaccinations and excess mortality in the Netherlands, led by Ronald Meester and Dr. Marc Jacobs, is now available online: Research Report: researchgate.net/publication/38…
This comprehensive study was made possible through a crowdfunding initiative by Stichting De Menselijke Maat. Alongside Dr. Marc Jacobs and Ronald Meester, the core research team included Bram Bakker, Jona Walk, and Jan Bonte. Given its depth, the report is extensive. Below is a concise overview of its key findings:
Chapter 1: Introduces the study and provides a justification for the research.
Chapter 2: Discusses excess mortality in the Netherlands, noting significant quantitative and qualitative changes since 2021.
Chapter 3: Presents data from AstraZeneca and the European Medicines Agency (EMA), raising concerns regarding vaccine safety.
Chapter 4: Covers their literature review and meta-analysis attempt. Out of 13,430 publications reviewed, only 83 met their stringent content and quality criteria. This finding suggests that "following the science" during the pandemic may not have always been prudent, given the varying efficacy rates and large uncertainty margins reported in the remaining studies.
Chapter 5: Focuses on a macro-level analysis of mortality related to vaccination. The findings suggest that vaccine effectiveness in the first four weeks post-administration may be negative, although the researchers exercise caution in their interpretations.
Chapter 6: Delves into micro-data from the Centraal Bureau voor de Statistiek (CBS) at an individual level. The researchers identified significant data artifacts that have potentially skewed all previous studies by both CBS and the RIVM (National Institute for Public Health and the Environment). The team refrains from speculating on the origins of this data contamination.
Chapter 7: Examines the reliability of the data used in their analysis, particularly focusing on CIMS and EMA data, which they found to be contaminated. This contamination complicates research efforts significantly.
Chapter 8: Explores the medical aspects of COVID-19 vaccinations, concluding that while side effects exist, their full extent remains unclear.
Chapter 9: Summarizes the research conclusions and offers recommendations for future studies.
This research represents a substantial contribution to the ongoing discussion about vaccine safety and public health during the COVID-19 pandemic.
All research transactions and data can be accessed through the following GitHub repository: GitHub Repository:
Dr Jacobs is a data scientist/ statistical consultant. Subject matter experts are finding their voice.linkedin.com/posts/dr-marc-…
Broken into layman's for everyone to enjoy.
Title: Uncovering the Truth: A Deep Dive into COVID-19 Vaccines and Excess Mortality in the Netherlands
Introduction
In the wake of the global COVID-19 pandemic, nations worldwide rushed to develop and distribute vaccines in hopes of curbing the spread of the virus and reducing mortality rates. The Netherlands, like many other countries, embarked on an ambitious vaccination campaign. However, as the dust began to settle, an unsettling pattern emerged: despite widespread vaccination, the country continued to experience unexplained excess mortality.
This puzzling phenomenon has sparked intense debate and raised crucial questions about the relationship between COVID-19 vaccines and overall mortality rates. In response to these concerns, a team of dedicated researchers, led by Ronald Meester and Marc Jacobs, undertook a comprehensive investigation. Their findings, detailed in a 166-page report, challenge many widely held beliefs about vaccine safety and efficacy.
Today, we'll take you on a journey through this groundbreaking research, breaking down complex scientific concepts into digestible insights that could reshape our understanding of public health policies and vaccine impacts.
The Unexpected Persistence of Excess Mortality
Before we delve into the heart of the research, let's first understand what we mean by "excess mortality." Simply put, excess mortality refers to the number of deaths from all causes during a crisis that exceeds what we would have expected under 'normal' conditions. It's a crucial metric in public health, often used to assess the full impact of pandemics or other widespread health crises.
In the Netherlands, a troubling trend emerged following the rollout of COVID-19 vaccines. Instead of seeing a reduction in overall mortality as vaccination rates increased, the country continued to experience higher-than-expected death rates. This persistence of excess mortality, even as COVID-19 cases declined, raised red flags for our research team.
Key questions emerged:
1. Could there be a connection between the COVID-19 vaccines and this ongoing excess mortality?
2. If such a connection exists, what mechanisms might be at play?
3. How reliable is the data we're using to make these assessments?
With these questions in mind, let's explore the key findings of this extensive research.
1. The Data Dilemma: Uncovering Inconsistencies
At the heart of any scientific investigation lies data - the foundation upon which conclusions are built and policies are shaped. However, our research team uncovered troubling inconsistencies in the datasets provided by key institutions, including the CBS (Central Bureau of Statistics), RIVM (National Institute for Public Health and the Environment), and EMA (European Medicines Agency).
These discrepancies aren't merely academic concerns. They strike at the very core of how we assess vaccine safety and efficacy. Let's break down some of the key issues:
a) Disappearing Data:
The team observed that in the EMA database, which tracks vaccine-related adverse events, some reports seemed to vanish over time. By regularly downloading and comparing datasets, the researchers noticed a consistent pattern of record removal. This raises serious questions about data integrity and the completeness of our understanding of vaccine side effects.
b) Misclassification Concerns:
One of the most alarming findings related to the classification of vaccinated individuals. The research suggests that some people who died shortly after receiving a vaccine may have been incorrectly classified as "unvaccinated" in official records. This potential misclassification could significantly skew our understanding of vaccine-related risks.
What's great about prion seeding?Did you know that the spike protein has 30 amyloidogenic motifs?But please continue to congratulate the mass murder of the West. Shipman doesn't hold a candle to Fauci
mRNA ribosomal frameshifting can occur when there's a shift in the reading frame during translation,
potentially leading to altered protein production.
frameshifting, could potentially contribute to the misfolding of proteins and thus indirectly play a role in prion formation
This comprehensive presentation, Kevin delves into the intriguing world of toxic peptides, amyloids, and prions, exploring their relevance to genetic vaccines and the SARS-CoV-2 virus. Broken into concise sections, he examines the potential implications and emphasize the importance of informed consent. This thread is a valuable resource worth saving. Kevin discusses the inflammatory and amyloidogenic effects of small sequences called epitopes, which can cause memory dysfunction in mice. They also mention a study that found the introduction of gene transfection technologies containing the spike protein can induce amyloidogenic cascades. Kevin highlights a 200% increase in the diagnosis of CJD in France after the rollout of vaccination programs, suggesting a potential link. They discuss the loss of cognitive function associated with exposure to the spike protein and propose that amyloidogenic disease processes may underlie long-haul COVID-19 symptoms. DR McCairn mentions the role of viral infections in facilitating intercellular aggregate dissemination and shares examples of misfolding prion amyloidogenic diseases
Amyloids and prions are real as are the neurological damage that comes with them.
The Tale of Misfolded Proteins: A Cascade Unleashed
Chapter 1: The Transfection Experiment
In a dimly lit laboratory, Dr. Evelyn Sterling, a brilliant geneticist, embarked on a groundbreaking experiment. She aimed to understand how transfections—introducing foreign DNA into cells—could trigger unexpected consequences. Her lab assistant, Alex, watched with anticipation as Dr. Sterling prepared her materials.
Dr. Sterling: “Alex, today we explore the intricate dance of proteins within cells. Our focus: amyloids and prion-like misfolding.”
Alex: “Fascinating! But why transfections?”
Dr. Sterling: “Because transfections can disrupt the delicate balance. Imagine a peaceful pond—the proteins are like water molecules. Transfections are like tossing a stone into the pond. Ripples form, and the entire ecosystem reacts.”
Chapter 2: The Misfolded Dance
Dr. Sterling transfected human cells with a modified gene encoding an amyloid precursor protein. As the cells absorbed the foreign DNA, the protein synthesis machinery went to work. But something went awry—the protein folded incorrectly.
Dr. Sterling: “Alex, observe. This misfolded protein is like a rogue dancer at a ball. It disrupts the choreography.”
Chapter 3: The Cascade Unleashed
The misfolded protein triggered a cascade. It interacted with other cellular proteins, distorting their shapes. Like dominoes falling, this led to more misfolding. The once-harmonious cellular ballet turned chaotic.
Dr. Sterling: “Alex, see how the misfolded protein recruits others? It’s like a rogue dancer pulling others into a frenzied waltz.”
Chapter 4: The Amyloid Aggregation
The misfolded proteins aggregated, forming amyloid plaques. These sticky clumps clogged cellular pathways, disrupting communication. Neurons struggled to function, leading to memory loss and cognitive decline.
Dr. Sterling: “Alex, these amyloids are like tangled shoelaces—cells stumble, and diseases emerge.”
Chapter 5: The Prion Twist
Dr. Sterling introduced another twist—the prion-like behavior. She transfected cells with a prion protein gene. The prion protein, once misfolded, acted as a template. It induced neighboring proteins to mimic its shape.
Dr. Sterling: “Alex, prions are like contagious dancers. They teach others their twisted steps.”
Chapter 6: The Infection Spreads
The prion-like misfolding spread. Neurons transformed, losing their normal function. Alex watched as the cells became ghostly, their connections severed.
Dr. Sterling: “Alex, this is how prion diseases propagate. Like a macabre dance, they infect neighboring cells.”
Epilogue: A Pathway Unveiled
Dr. Sterling’s research revealed the intricate pathways of protein misfolding. Transfections, like stones in a pond, set off cascades. Amyloids and prion-like diseases emerged, leaving a trail of disrupted cells.
And so, in the quiet of her lab, Dr. Sterling whispered, “We’ve glimpsed the secrets of life’s dance—a choreography both beautiful and treacherous.”
Mechanisms of protein-folding diseases at a glance