Spike Detox by Measslainte is a meticulously crafted blend of nature's finest ingredients. Our ancient old-growth pine needle tea, delicately infused with the flowering buds of foxglove, is expertly combined with a harmonious medley of premium components. This exclusive formula includes loinsmane mushrooms, seamoss, bladderwrack, invigorating natural peppermint, quercetin for added antioxidants, bromelain for digestive support, the cholesterol-balancing power of red yeast rice, CoQ-10 for heart health, NAC for detoxification, the exotic graviola soursop, the liver-loving milk thistle, and chelated zinc for overall wellness. Experience the revitalizing effects of Spike Detox and embark on a journey to enhanced well-being
Fasting is a practice that has gained significant attention in recent years due to it's health benefits. When you are feeling unwell, understanding the significance of fasting can be crucial. You can read more about it in this article: , fruit fasting is another viable option to explore. It's a method of fasting that involves consuming only fruits for a specified period. This approach can have its unique advantages, and it's worth considering as part of your wellness routine."Grounding: How Just 15 Minutes a Day Can Change Your Life"Grounding, also known as earthing, is a simple yet powerful practice. Devoting just 15 minutes a day to grounding can have a profound impact on your overall well-being. The best part is that it costs nothing. To learn more about the benefits and how to get started with grounding, check out this informative article: measslainte.ie/post/water-fas… measslainte.ie/post/grounding…
#Cucumber #Silca #Detox #Nutrition
cucumbers stand tall as a versatile, nutrient-packed superfood. With their myriad benefits, from connective tissue support to silica-rich skin enhancement and detoxifying properties, cucumbers are your allies in the quest for vibrant health
The results indicate that nanoporous silica, which has been functionalized with organic ligands, possesses substantial potential as a versatile material in the realm of detoxification therapies.
Parsley tea has been traditionally used as a natural remedy for various health issues, including detoxifying the kidneys. The kidneys play a crucial role in filtering waste products and toxins from the body, and they can be affected by various factors such as diet, medication, and environmental pollutants.
Parsley contains various compounds such as flavonoids and volatile oils, which have been shown to have diuretic and anti-inflammatory properties. These properties can help increase urine output and promote the elimination of toxins from the body, thus reducing the workload on the kidneys.
To make parsley tea, you can follow these simple steps:
Wash a bunch of fresh parsley leaves thoroughly and chop them into small pieces. Add the chopped parsley to a teapot or a cup. Pour boiling water over the parsley leaves. Cover the teapot or cup and let it steep for 5-10 minutes. Strain the tea and drink it warm or cold. It is important to note that parsley tea should not be used as a replacement for medical treatment, and people with kidney problems should consult their healthcare provider before using it. Additionally, excessive intake of parsley tea may cause side effects such as stomach upset, diarrhea, and allergic reactions. Therefore, it is recommended to consume it in moderation.
Benefits of Glutathione#
Glutathione has numerous health benefits, including:
Antioxidant Protection
Glutathione is a powerful antioxidant that protects the body against oxidative stress and free radical damage.
Detoxification
Glutathione plays an important role in the detoxification of harmful toxins and chemicals in the body.
Immune Function
Glutathione is essential for the proper functioning of the immune system. It helps to boost the immune response and protect against infections.
Anti-Aging
Glutathione is believed to have anti-aging properties due to its ability to protect the body against oxidative stress and free radical damage.
Post-vaccination syndrome (PVS), also referred to as post-acute sequelae following COVID-19 vaccination, describes a set of persistent symptoms reported by a subset of individuals after receiving mRNA COVID-19 vaccines. Emerging research from 2022–2026 explores potential biological mechanisms behind these symptoms in affected people. This overview synthesizes peer-reviewed evidence, including studies on spike protein dynamics, microclots, prion-like elements, immune changes, and manufacturing concerns. It draws from a range of sources, to provide a balanced view. Note that PVS remains understudied and is not formally recognized by major health authorities like the FDA or WHO, but preliminary data suggest real physiological changes in some cases. I dont know anyone who regrets not taking the jabs :)
Understanding Post-Vaccination Syndrome: A Science-Based Overview
When COVID-19 mRNA vaccines were introduced, they were designed to deliver temporary instructions for cells to produce the spike protein, triggering an immune response. However, emerging research suggests that for some individuals, this process may not follow the expected trajectory. This has led researchers to investigate a constellation of symptoms now being studied as "post-vaccination syndrome" or "post-acute sequelae" following vaccination.
This explanation draws from peer-reviewed research published between 2022 and 2026 to help understand what scientists are currently investigating.
Core Concepts
1. Spike Protein Persistence
The Expected Process:
After mRNA vaccination, the spike protein should be cleared from the body
within days to weeks. Think of it like a temporary instruction manual that
gets used and discarded.
What Research Shows:
Studies indicate that for some people, spike protein may persist far
longer than anticipated:
"Expression of SARS-CoV-2 spike protein in cerebral arteries"
(pubmed.ncbi.nlm.nih.gov/40184822/) detected spike protein in
brain blood vessels months after vaccination. Similarly, news.yale.edu/2025/02/19/imm…
indicate-future-research-directions is investigating persistent spike
protein in individuals with post-vaccination syndrome.
A nature.com/articles/s4154… confirmed mRNA can
persist up to 30 days, while cell.com/cell-host-micr…
found spike protein at the skull-meninges-brain interface, potentially
linked to ongoing neuroinflammation.
Analogy: Imagine leaving your car running after you arrive at your
destination. The engine (spike protein) was meant to shut off, but it's
still idling—and in some cases, revving—in ways that may cause problems.
Claim: “Biodistribution is limited to muscle and draining lymph node.”
PMDA (Japan, Pfizer approval report, 2021):
“After intramuscular administration, LNP lipids (ALC-0159/0315) were rapidly distributed to the liver within 24 hours, accounting for ~20–60% of the dose.”
TGA (Australia, nonclinical evaluation, 2021):
“Luciferase expressed by the LNP-8-mRNA drained to the liver, visualised at 6 h post-injection; signal declined and was gone by 48 h.”
Frameshift/unintended proteins was one flawed paper; never seen elsewhere.”
What the literature actually says
Primary study (Nature, 2024 — Cambridge/Oxford team):
“…incorporation of N¹-methylpseudouridine into mRNA results in +1 ribosomal frameshifting in vitro and that cellular immunity in mice and humans to +1 frameshifted products… occurs after vaccination.”
PubMed (abstract): pubmed.ncbi.nlm.nih.gov/38057663/
Nature (HTML): nature.com/articles/s4158…
Nature Reviews (2024) — independent review summarizing the Nature paper:
“…recent findings indicate that m¹Ψ promote low levels of +1 ribosomal frameshifting on the COVID mRNA vaccine sequence…”
(Open-access) pmc.ncbi.nlm.nih.gov/articles/PMC11…
Nature Reviews Drug Discovery — News & Views (2024) on the same result:
“…incorporation of 1-methylΨ into mRNA… results in ribosomal frameshifting, producing frameshifted polypeptides that… elicit an off-target cellular immune response… in mice and humans.” nature.com/articles/d4157…
Peer-reviewed overviews (2024) noting the same phenomenon:
“…N1-methylpseudouridine can lead to +1 ribosomal frameshifting during translation…”
(Open-access review) pmc.ncbi.nlm.nih.gov/articles/PMC11…
Ireland’s Constitution is clear: the State must defend the life and person of its People (Art. 40.3.2).
Instead, you forced DNA-contaminated, SV40-laced mRNA injections on the nation.
🔹 Peer-reviewed studies show plasmid DNA + SV40 promoter sequences in vials.
🔹 Pathology confirms spike protein in vital organs up to 17 months later.
🔹 Scientists link spike to amyloid clots, strokes, myocarditis & cancer.
This is not “theoretical risk” it is hard evidence.
We demand:
1. Immediate suspension of mRNA jabs.
2. A forensic audit of every batch.
3. A full public inquiry into excess mortality.
Ireland’s sovereignty is not for sale.
The People are the guardians of the Constitution and we will hold you to account.
The current “safe limit” for aluminum in vaccines (~0.85 mg per dose) wasn’t set using modern safety studies or toxicology. It actually comes from old vaccine practices in the mid-1900s, when they were just testing what made vaccines more effective.
A 2025 review shows there’s no real toxicology or pharmacokinetic science behind this number. it’s not based on how aluminum actually behaves in the body.
Q: Why are we still using efficacy-era thresholds to claim safety in infants?
A big 2025 study (Annals) looked at health records from 1.22 million children, tracking aluminum exposure from vaccines before age 2. They reported mostly no associations across 50 different health outcomes.
The study left out diagnoses before age 2 the most critical early window. And they didn’t compare vaccinated kids to the unvaccinated group directly, which could have been the strongest test.
Q: If the dataset had ≈15k unvaccinated, why not show that comparison transparently?
The study actually found a signal for Asperger’s risk was about 1.67x higher per mg of aluminum (2007–2018 births).
Instead of digging deeper, the authors brushed it off as “chance” and blamed overlap issues in the data. When they restricted the analysis to later births, the signal disappeared.
Fine but the obvious next step is to replicate with a proper design (pre-registered overlap checks, latency controls, and false-discovery corrections).
Q. why was the instinct to dismiss the finding, rather than design the follow-up that could confirm or rule it out?
Kevin McKernan
Profession: Founder of Medicinal Genomics, Genomics Researcher, US
Date First Reported: 2023-02
Key Details: Detected 225-843ng/dose residual plasmid DNA including SV40 promoter in Pfizer/Moderna vials using qPCR/fluorometry; exceeds regulatory limits; integration concerns.
Sharable Link: osf.io/mjc97/
Tomonori Nitta
Profession: Researcher at Tokyo University, Japan
Date First Reported: 2023-11
Key Details: Found 17.5-81.9ng/dose DNA in Japanese Daiichi-Sankyo vials; SV40 detected, including in tumors via cell transfection
Sharable Link: pmc.ncbi.nlm.nih.gov/articles/PMC12…
Phillip Buckhaults
Profession: Professor at University of South Carolina, Cancer Genomics Expert, US
Date First Reported: 2023-09 (testimony), 2024-04 (data)
Key Details: qPCR showed 1.5-18.7ng/dose plasmid DNA with SV40 promoter; observed integration into human stem cells; presented to SC Senate.
Sharable Link: scstatehouse.gov/CommitteeInfo/…
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)