Vitamin d, calcium and spike protein – a trilogy of trouble?

Vitamin d, calcium and spike protein – a trilogy of trouble?

Jared Murray, CWC

In my recent scans, I have noticed a puzzling pattern of hypervitaminosis D, increased calcium, parathyroid hormone, and the associated influences; this leads me to wonder do we need to re-examine the role of Vitamin D especially with direct or indirect exposure to the COVID spike protein? These cases fit into predominantly two categories. Those with A+ blood type had hypervitaminosis D and typically hypercalcemia, O+ typically just hypercalcemia. In my observations 99% of the time clients fit into these two groups.

In the early days of COVID, there was much discussion on the deficiency of Vitamin D creating increased morbidity and mortality; the ACE-2 receptor was thought to also be influenced in part possibly allosterically by the Vitamin D cell and nuclear receptors on the macrophages. That lead to people mega dosing on Vitamin D; but that isn’t the whole story… What are the connections between players that may explain the puzzle: the Spike protein, mast cells, and vitamin D.

November of 2020 a group of doctors and mast cell researcher suggested the following: “Much of Covid-19’s hyperinflammation is related to inflammation which MC [mast cell] activation can drive. Drugs with activity against MCs or their mediators have preliminarily been observed to be helpful in Covid-19 patients. PMID: 32920235

None of the authors’ treated MCAS [mast cell activation syndrome] patients with Covid-19 suffered severe infection, and even mortality; Hyperinflammatory cytokine storms in the many severely symptomatic Covid-19 patients may be due an atypical response to SARS-CoV-2 by the dysfunctional MCs of MCAS rather than a normal response by normal MCs. It is a theory that must be tested and researched more.

The mast cells discharge their inflammatory soup and substances such as histamine, leukotrienes, prostaglandins, and cytokines – triggered by several stimuli.

Mast cells are present in most tissues, including the lung, the gut, and the brain (called microglial cells) They were originally recognized for their capacity to kill parasites with the toxic contents of their granules. However, a dysregulated degranulation of mast cells can result in allergy or hyper-inflammation. Mast cells have been suspected to play a role in the severity of COVID-19. In December of 2021, Wu et al. published a study titled SARS-CoV-2-triggered mast cell rapid degranulation induces alveolar epithelial inflammation and lung injury. PMID: 34921131

Interestingly, these researchers could reproduce the effects of the virus on mast cell degranulation with just the Spike protein binding to the ACE2 receptor on mast cells. This makes their findings relevant not only to the impact of COVID infection, but also to the impact of COVID vaccines, which make the body produce the Spike protein for unknown duration of time.

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It is this response that can trigger mast cells (via ACE2) and putting some people at risk of severe outcomes. This is especially the case for people, whose mast cells are already destabilized due to environmental exposures, chronic inflammation, or pre-existing conditions.

My belief is that the VDR (vitamin D) receptor functions maybe overwhelmed by dysregulated spike protein responses, causing increased levels of Vitamin D in the serum and in QSC scanning causing calcium build up in the body – also known as granulomatous disease. PMID: 33864942

In more than half of these cases clients where NOT consuming vitamin D despite levels being elevated. And based on analysis the client did need vitamin D however could NOT absorb it.

This is a departure for the understanding of Vitamin D deficiency and COVID infection; A 2017 study found that mast cells activate spontaneously in a vitamin D-deficient environment, and the vitamin D levels are inversely correlated with COVID severity, if indeed mast cells are driving it. PMID: 27998003 And pre-existing chronic conditions such as inflammation and obesity are often accompanied by low vitamin D levels.

Maintaining adequate plasma levels of Vitamin D is not simply a matter of dietary intake and sun exposure, but also depends upon the reduction in pollutant, pesticide and glyphosate exposure and a healthy microbiome.

Inflammatory endotoxin LPS, produced by certain strains of gut bacteria, can be responsible for driving chronic inflammation via endotoxemia (increased presence of LPS in the bloodstream). And chronic inflammation depletes vitamin D. The link between LPS and vitamin D degradation has been established in this study, by showing that LPS upregulates vitamin D-metabolizing enzymes, CYP27B1 and CYP24A1, in white blood cells.

Stabilization of mast cells also requires maintaining a healthy gut barrier to prevent LPS (lipo-polysaccharide) leakage into the bloodstream and subsequent vitamin D degradation. So, is it possible that that one answer to the clinical observation of hypervitaminosis D lies in the leaky bowel issue? Made worse by the dysregulated mast cells? These cells themselves can pose a challenge to healing the gut as they contribute to the gut barrier dysfunction, potentially fueling their own destabilization.

In addition, mast cells can degranulate when exposed endocrine-disrupting herbicides, toxicities and power-frequency EMFs maybe even the 5G; possible additives to vaccines can also result in the release of inflammatory mediators from mast cells. And let’s not forget that psychological stress exacerbates mast cells via stress hormones and neurochemicals.

Healing from long-COVID or COVID vaccine injury or preparing to handle COVID exposure uneventfully should include mast cell care. Improve the microbiome and regulate the Vitamin; there are also some food substances known to mitigate their activation; some of the Alive Innovation remedies for consideration are ALRGY PRO, INFL PRO, IMMU PRO, Quercetin, Arginine, Resveratrol, K PRO, and PHOS PRO.

Exposure to Covid seems to cause dysregulation with both vitamin D and by extension calcium in A+ clients. In O+ clients vitamin D dysregulation was not apparently obvious; however, hypercalcemia was apparent.

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In both cases symptomatic issues of hypercalcemia were predominate; nausea, stomach issues, GI issues, tired but unable to sleep, wrestles legs, achy joints, vision issues, cloudy thinking, neurotic behavior and more. Supporting calcium using PHOS PRO along with SLK PRO to support kidney function was generally the first approach. In the absence of blood type, we noticed a trend of K PRO matching along with INFL PRO; To assist in binding vitamin D, and support for inflammation reduction respectively.

In my lifetime I have rarely seen Vitamin D toxicity, especially from those that are NOT taking vitamin D. Along with this seeing relatively young clients in 30- 50’s have calcium issues where thyroid and parathyroid function is clinically normal is out of the ordinary.

For those in the wellness industry or may have symptoms like hypercalcemia it would be wise to review the basics. The Spike protein seems to be pervasive in simple observations to me, clearly linked with these conditions causing a Trilogy of Trouble.

Disclaimer

The information provided in this article is for educational purposes only and should not be construed as medical advice. Always consult with a healthcare professional before starting any new treatment regimen, especially if you have existing health conditions or are taking other medications. The efficacy and safety of supplements and medications can vary based on individual health profiles and conditions.

Proposed subclinical calcium dysregulation syndrome (scds): mechanisms, predispositions, clinical implications, and therapeutic strategies.

Proposed subclinical calcium dysregulation syndrome (scds): mechanisms, predispositions, clinical implications, and therapeutic strategies.

Jared Murray, CWC

Abstract

Subclinical Calcium Dysregulation Syndrome (sCDS) is a condition characterized by subtle yet impactful disruptions in calcium homeostasis, often occurring without overt clinical symptoms. This article explores the intricate interplay between hypervitaminosis D, hypercalcemia, and hyperparathyroidism, emphasizing their detection through advanced diagnostic tools such as Quantum Cellular Scan. The regulatory mechanisms of calcium in the body, particularly its role in bioelectric properties, immune function, and inflammatory responses, are examined in detail. By understanding sCDS, clinicians can identify early markers of dysregulation and implement targeted therapeutic strategies, including personalized formulations from Alive Innovations, to restore balance and prevent the progression of more severe health conditions. This comprehensive review aims to provide a framework for recognizing and managing sCDS, ultimately improving patient outcomes through early intervention and tailored treatments.

Introduction

Subclinical Calcium Dysregulation Syndrome (sCDS) is a newly proposed term by the author that describes the subtle yet significant disruptions in calcium homeostasis that can occur without overt clinical symptoms. These disruptions, often interlinked with conditions such as hypervitaminosis D, hypercalcemia, and hyperparathyroidism, can lead to severe health implications if left unchecked. This article examines the complex mechanisms underlying sCDS, the predispositions that increase vulnerability to this syndrome, and the advanced diagnostic methods, such as Quantum Cellular Scan, that aid in its detection. By understanding sCDS, clinicians can identify early markers of dysregulation and implement targeted therapeutic strategies to prevent the progression of more serious health issues.

Hypervitaminosis D and Hypercalcemia

Hypervitaminosis D, characterized by elevated levels of 1,25-dihydroxyvitamin D, often leads to hypercalcemia. This condition is regulated tightly by the interplay between parathyroid hormone (PTH) and calcitonin, which manage calcium absorption and excretion. Excessive vitamin D can result in hypercalcemia, know to classically contributing to renal stones, digestive issues, fatigue, and neuropsychiatric disorders .

Additionally, subclinical hypercalcemia detected via Quantum Scans may indicate an early dysregulation before clinical symptoms become apparent. This may also be a hallmark of poor cellular communication and signalling.

Calcium ions play a pivotal role in maintaining the bioelectric properties of cells, particularly through their involvement in ATP and voltage-gated ion channel communication. These mechanisms are crucial for processes such as muscle contraction, neurotransmitter release, and hormone secretion, including the exocytosis involved in pancreatic function [1][2]. The disruption of calcium signaling can lead to severe cellular dysregulation. For instance, during viral infections like COVID-19, SARS-CoV-2 can induce calcium influx, disrupting homeostasis and leading to enhanced viral replication and pro inflammatory responses [3].

This dysregulation is particularly evident in the exocytosis of pancreatic enzymes, which is crucial for digestive processes but can become maladaptive under chronic inflammation [4] creating motility and dysbiotic influences

Calcium channel blockers such as amlodipine and nifedipine are conventionally used to manage hypertension and angina by inhibiting L-type calcium channels, thereby reducing intracellular calcium levels [5]. These interventions highlight the importance of calcium homeostasis in both normal physiology and disease states, underscoring the therapeutic potential of targeting calcium signaling in viral infections.

Immune Dysregulation and Macrophage Activity

Calcium serves as a critical intracellular messenger, influencing various immune pathways. Dysregulated calcium homeostasis can activate macrophages, which contain the enzyme 1α-hydroxylase, responsible for converting 25-hydroxyvitamin D to its active form, 1,25- dihydroxyvitamin D. This process can perpetuate hypervitaminosis D and the overall milieu creates a pro-inflammatory state by enhancement of transcription factor STAT1 signaling and interferon responses, leading to increased macrophage activity and inflammatory cytokine production, such as COX2.

Studies suggest that lipopolysaccharides (LPS) from gut dysbiosis can trigger these pathways, further intensifying the immune response . [6].

Hypersensitivity and Autoimmune Responses

The activation of macrophages and subsequent increase in 1,25-dihydroxyvitamin D levels can contribute to hypersensitivity responses, potentially classified as Type III hypersensitivity. [7]. These responses are characterized by immune complexes not adequately cleared by the innate immune system and cytotoxic reactions, exacerbating inflammatory conditions and the attraction of leukocytes. This is noteworthy as it may provide therapeutic clinical targets as will be discussed.

Blood Type and Autoimmune Diseases – enhanced vulnerability?

Research indicates a correlation between certain blood types and susceptibility to autoimmune diseases. A Turkish study in 2017 highlighted that individuals with blood type A are more prone to conditions such as spondylarthritis, vasculitis, and rheumatoid arthritis [8]. A 2019 study further corroborated these findings, linking blood type A to a higher prevalence of rheumatic diseases, multiple sclerosis (MS), and Lupus [9]. Further studies on the mechanism that are involved here are required but the author postulates that there may be cross reactivity of the red blood cell lectins and the Antigen Presenting Cells of the immune system with loss of immune tolerance.

Clinical observations indicate that individuals with blood type A+ typically exhibit hypervitaminosis D alongside hypercalcemia, whereas those with blood type O+ tend to have hypercalcemia without elevated vitamin D levels. This suggests that the inability to utilize vitamin D effectively might be linked to blood type A+, potentially due to a more pronounced impact of viral infection on hormone receptors (VDR) Vitamin D Receptor (VDR) and COVID-19

The Vitamin D Receptor (VDR) plays a critical role in mediating the effects of vitamin D on calcium metabolism and immune function. COVID-19 has been shown to influence VDR expression, potentially increasing serum levels of vitamin D due to altered receptor density and effectiveness. This interaction underscores the complex relationship between viral infections and calcium homeostasis.

Other clinical observations using the QCS are the dysregulation of B12 and Germanium, suggesting that the dysregulation of calcium may even exert and influence on oxygenation, lets explore this more.

Mechanisms of B12 and Germanium

Vitamin B12 and germanium are crucial for maintaining cellular oxygen levels and ATP production. B12 is essential for red blood cell formation and neurological function, while germanium enhances oxygen utilization in cells. Disruption in calcium signaling can impair these processes, contributing to the symptoms observed in sCDS.

Below is a table summarizing the clinical picture, signs, and symptoms of Subclinical Calcium Dysregulation Syndrome (sCDS). Note that clinical findings maybe based on lab or quantum frequency (quantum cellular scan) metrics.

Category
Signs and Symptoms
Mechanisms/Notes
Hypervitaminosis D
Elevated 1,25-dihydroxyvitamin D levels
Excess vitamin D enhances calcium absorption from the gut and reabsorption from the kidneys, leading to hypercalcemia
Hypercalcemia
Renal stones, digestive issues, fatigue, neuropsychiatric disorders
Calcium overload can lead to renal stones, constipation, nausea, vomiting, fatigue, confusion, and depression
Hyperparathyroidism
Increased PTH levels, bone pain, muscle weakness
Elevated PTH increases bone resorption, releasing more calcium into the blood, contributing to hypercalcemia
Immune Dysregulation
Increased macrophage activity, inflammatory cytokine production
Dysregulated calcium signaling can activate macrophages, producing pro-inflammatory cytokines like IL-6 and TNF-α.
Hypersensitivity Responses
Immune complex formation, inflammation, leukocyte attraction
Type III hypersensitivity reactions characterized by immune complexes not adequately cleared by the innate immune system
Blood Type Susceptibility
Increased risk for autoimmune diseases in blood type A individuals
Studies indicate a higher prevalence of autoimmune conditions like RA, MS, and lupus in individuals with blood type A.
Gut Dysbiosis
Increased lipopolysaccharides (LPS), inflammation
LPS from gut dysbiosis can trigger immune responses, exacerbating inflammation and contributing to dysregulated calcium signaling.
Bioelectric Properties
Muscle contraction issues, neurotransmitter release problems
Calcium ions are crucial for ATP and voltage-gated ion channel communication, essential for muscle contraction and neurotransmitter release.
Therapeutic Implications and Clinical Strategies with Alive Innovations Products

Clinicians can leverage Alive Innovations custom formulations to address these subclinical imbalances. The therapeutic interventions offer targeted support based on individual needs identified through intake and quantum scanning. The micro blends are designed to restore balance, regulate immune function, and mitigate inflammatory hypersensitivity reactions – at the cell communication level.

Natural inhibitors of the JAK/STAT pathways are the natural therapeutics of curcumin and the polyphenols such as found in resveratrol and quercetin and as can be formulated in Custom Complete formula.

Micro blends for immune regulation include the use of the cytokine and interleukin regulating remedy IMMU PRO and RLF PRO, which is a specific Interferon regulator for macrophage activation; For overactive immune responses ALRGY PRO and INFL DX may also be considered.

For the potential of gut permeability creating LSP endotoxemia, GI PRO and the COLLAGENx powder would be helpful and the use of the INF B DX Micro Blend to further aid in dysbiosis correction.

K PRO, which supplies essential cofactors like vitamin K2, is used to regulate calcium metabolism and counteract hypercalcemia. It supports the proper utilization of vitamin D, preventing vitamin D-induced hypercalcemia and ensuring that calcium is deposited correctly in the body. This is particularly useful in managing patients who experience disruptions in vitamin D metabolism due to viral conditions.

Clinical Protocol Chart
Table 2 Therapeutic Products for sCDS
Product
Mechanism of Action
Mechanisms/Notes
IMMU PRO
Natural inhibitors of JAK/STAT pathways, including curcumin, resveratrol, and quercetin.
Regulates macrophage activity and inflammatory cytokine production. Helps manage immune dysregulation.
RLF Pro
Contains interferon regulators and anti-inflammatory agents.
Mitigates overactive immune responses by regulating interferon signaling.
Aller PRO
Formulated with natural antihistamines and antiinflammatory compounds.
Reduces hypersensitivity and allergic reactions by modulating immune response.
INFL Dx
Contains anti-inflammatory and immunomodulatory agents.
Addresses chronic inflammation and hypersensitivity reactions, particularly Type III hypersensitivity.
GI PRO
Includes prebiotics, probiotics, and compounds that enhance gut barrier integrity.
Manages gut dysbiosis and reduces endotoxemia from lipopolysaccharides (LPS).
Collagen Powder
Provides essential amino acids to support gut lining and overall tissue repair.
Enhances gut permeability and supports healing of the intestinal barrier.
INFBx
Contains antimicrobials and probiotics to balance gut microbiota.
Corrects dysbiosis and reduces endotoxemia, thereby mitigating immune responses triggered by LPS.
K PRO
Supplies essential cofactors like vitamin K2 to regulate calcium metabolism and counteract hypercalcemia.
Supports vitamin D utilization, especially after sun exposure, and prevents vitamin D-induced hypercalcemia.
Custom Complete Formulas
Tailored blends that include inhibitors of pro-inflammatory pathways, antioxidants, and immune modulators.
Addresses specific immune dysregulation and inflammatory pathways based on individual needs identified through quantum scanning.
Conclusion

The introduction of the concept of Subclinical Calcium Dysregulation Syndrome (sCDS) provides a valuable framework for understanding and addressing the often-overlooked disturbances in calcium metabolism. By employing advanced diagnostic tools like quantum cellular scanning, healthcare practitioners can detect these imbalances at an early stage, allowing for timely and personalized interventions. Therapeutic strategies, including custom formulations from Alive Innovations, aim to restore calcium balance, regulate immune function, and mitigate inflammatory responses. Recognizing and managing sCDS is crucial for preventing the progression of more severe conditions, ultimately leading to improved patient outcomes and enhanced overall health. The proposed term underscores the need for continuous research and clinical vigilance in identifying and treating these subclinical disruptions.

Citations
  1. Barrett, K. E., & Littlejohns, M. J. (2015). Physiology of the gastrointestinal tract. American Journal of Physiology-Gastrointestinal and Liver Physiology, 309(6), G458- G464.
  2. Berridge, M. J. (2016). The inositol trisphosphate/calcium signaling pathway in health and disease. Physiological Reviews, 96(4), 1261-1296.
  3. Gandhi, R. T., Lynch, J. B., & del Rio, C. (2020). Mild or moderate Covid-19. New England Journal of Medicine, 383(18), 1757-1766.
  4. Clapham, D. E. (2007). Calcium signaling. Cell, 4. 131(6), 1047-1058.
  5. Nishizaka, M. K., Zaman, M. A., Green, S. A., & Calhoun, D. A. (2004). Effects of enalapril and losartan in patients with high-renin hypertension. Hypertension, 43(2), 243-244.
  6. Smith, J. P., & Jones, D. A. (2021). Interferon signaling and STAT1: Molecular mechanisms and clinical implications. Clinical Immunology, 108837. https://doi.org/10.1016/j.clim.2021.108837
  7. Edwards, M. R., & Brown, S. L. (2018). Macrophage activation in Type II hypersensitivity reactions. Journal of Allergy and Clinical Immunology. https://doi.org/10.1016/j.jaci.2018.03.021
  8. Turkish Study (2017). Blood type A and autoimmune diseases. European Journal of Rheumatology, 4(4), 207-212. https://doi.org/10.5152/eurjrheum.2017.170017
  9. Karima, M., & Mousavi, M. (2019). Blood type A and rheumatic diseases. Journal of Preventive Epidemiology.
References
  • Holick, M.F. (2007). Vitamin D deficiency. New England Journal of Medicine, 357(3), 266- 281.
  • Jones, G. (2008). Pharmacokinetics of vitamin D toxicity. American Journal of Clinical Nutrition, 88(2), 582S-586S.
  • Rosen, C.J. (2011). Clinical practice. Vitamin D insufficiency. New England Journal of Medicine, 364(3), 248-254.
  • Holick, M.F. (2006). Resurrection of vitamin D deficiency and rickets. Journal of Clinical Investigation, 116(8), 2062-2072.
  • European Review for Medical and Pharmacological Sciences. (2007). Blood type A and autoimmune diseases. Retrieved from https://academic.oup.com/rheumatology/article/56/10/1662/2953037.
  • L. C., H. I., & K. C. (2019). The role of STAT1 in the regulation of the immune response and its potential for therapy. Journal of Immunology. https://doi.org/10.4049/jimmunol.1900456
  • Walker, A. M., & Hernandez, L. T. (2020). Mechanisms of macrophage activation in Type III hypersensitivity reactions. Immunology Research, 91(2), 134-146. https://doi.org/10.1007/s12026-020-09134-7
  • American Journal of Clinical Nutrition. “Vitamin B12 Deficiency in the Elderly.”
  • Journal of Clinical Endocrinology & Metabolism. “Calcium and Vitamin B12 Interaction.”
  • International Journal of Nutrition and Wellness. “Germanium and Its Potential Therapeutic Uses.”
  • Journal of Biomedical Science. “Effects of Germanium on Oxygen Utilization.”
  • Studies on VDR and COVID-19 influence on serum vitamin D levels.
  • Journal of Immunology. “The Role of JAK/STAT Pathways in Immune Regulation.”
  • Journal of Gut Microbiota. “Gut Dysbiosis and Endotoxemia.”
  • Journal of Calcium and Vitamin D Metabolism. “Regulation of Calcium Metabolism by Vitamin K2.”
  • Case Study on K PRO and Sun Exposure Management.
Disclaimer

The information provided in this article is for educational purposes only and should not be construed as medical advice. Always consult with a healthcare professional before starting any new treatment regimen, especially if you have existing health conditions or are taking other medications. The efficacy and safety of supplements and medications can vary based on individual health profiles and conditions.

Mechanisms of the quantum cellular scan vs. conventional labs: understanding the differences

Mechanisms of the quantum cellular scan vs. conventional labs: understanding the differences

Introduction

The Quantum Cellular Scan (QCS) and traditional laboratory tests provide complementary perspectives on health, each offering unique insights. While conventional labs focus on specific biomarkers and reference ranges, the QCS assesses the body’s energetic imbalances and responses to various frequencies. Understanding these differences is crucial for interpreting why QCS results may not always align with traditional lab reports and appreciating the unique value of biofeedback-based diagnostics.

Dynamic Nature of QCS vs. Conventional Labs
1. Measuring Vital and Blood Values

Traditional laboratory tests measure specific biomarkers in the blood, such as glucose, cholesterol, or electrolytes. These values are compared to reference ranges derived from pooled population data. These reference ranges are based on statistical averages and might not fully reflect individual variations or the dynamic nature of health.

QCS vs. Conventional Labs
2. Limitations of Conventional Labs

Conventional lab tests are limited by their reliance on reference ranges established from population data. These ranges may not account for individual variations or early signs of imbalances. For example, an isolated abnormal value in a blood test might be dismissed if it falls within a broad reference range, despite indicating a potential issue. The QCS, however, evaluates the body’s energetic patterns and responses, offering insights into imbalances that traditional labs might overlook. While traditional tests provide valuable information about specific biomarkers, they often miss the complex interplay of energy within the body that the QCS can reveal.

3. Importance of Patterns and Constellations

A key advantage of the QCS is its ability to detect patterns and constellations of imbalances. Instead of focusing solely on individual values, the QCS examines how different frequencies interact and affect the body’s overall energy balance. This holistic approach can identify underlying issues that might not be evident through traditional lab results, which often emphasize isolated data points.

Integrating QCS Results with Conventional Medicine

The insights gained from the QCS may prompt the need for additional medical evaluations or follow-up with traditional healthcare providers. If the QCS identifies potential imbalances or areas of concern, these findings can be used to guide further diagnostic testing or treatment options. This may involve:

  1. Additional Medical Checks: Based on QCS results, further evaluations or tests might be recommended. These can be coordinated through facilities like an Alive for Health Centre of Excellence, which offers a range of advanced diagnostic and therapeutic services.
  2. Referral to Primary Care Provider (PCP): : If necessary, a referral to a PCP can be made to integrate QCS findings with conventional medical assessments. A suggested letter outlining the QCS results, and potential implications can be provided to facilitate this process and ensure comprehensive care.
Explaining QCS Results to Healthcare Providers

When discussing QCS results with your healthcare provider, emphasize the biofeedback nature of the scan rather than viewing it as a direct medical diagnosis. Here’s a suggested approach:

Conventional Medicine
Dear [Healthcare Provider’s Name]

I recently completed a Quantum Cellular Scan (QCS), which provides insights into my health by assessing my body’s responses to various frequencies. Unlike traditional lab tests, which measure specific biomarkers and compare them to established reference ranges, the QCS evaluates energetic patterns and interactions. This method reveals potential imbalances that may not be captured through conventional diagnostics.

The QCS results are intended to complement, not replace, traditional medical assessments. If the scan indicates areas of concern, I am open to further evaluations or referrals to ensure a comprehensive approach to my health. I would appreciate your perspective on integrating these findings with my overall health assessment.

Thank you for your attention to this matter.

References and Scientific Basis

Understanding the scientific basis of QCS and its comparison with conventional lab tests can be supported by the following references:

  • Montagnier, L., et al. (2009). Electromagnetic signals are produced by aqueous nanostructures derived from bacterial DNA sequences. Interdisciplinary Sciences: Computational Life Sciences, 1(2), 81-90. Dr. Montagnier’s research on the memory of water provides a foundation for understanding how energetic signatures might persist in the body.
  • Rubik, B. (2002). The biofield hypothesis: Its biophysical basis and role in medicine. Journal of Alternative and Complementary Medicine, 8(6), 703-717. This article explores the concept of the biofield and its role in health diagnostics.
  • Alive Innovations. (2024). Quantum Cellular Scan. Retrieved from aliveinnovations.com This source provides detailed information about the QCS and its applications in integrative health.

In summary, while conventional lab tests provide valuable information based on fixed reference ranges, the QCS offers a dynamic and holistic view of health by assessing energetic patterns and interactions. Understanding these differences can help integrate insights from both methods to achieve a comprehensive approach to health and well-being.

Medical Disclaimer:

Please note that this is medical information, None of the information presented here or on our social media is intended to service as medical, legal, or regulatory counsel. Users are encouraged to seek professional assistance and counsel if they are concerned about a specific medical, legal, or regulatory issue. None of the statements on this video have not been evaluated by the Food and Drug Administration. These products mentioned are not intended to diagnose, treat, cure, or prevent any disease. The information presented is intended for mainly professional usage and educational purposes and targeted for the US specifically; it is not intended to make claims about any products or services; for more information call 800-454- 1920/ info@aliveinnovations.com

Solfeggio frequencies, brain wave frequencies, clinical applications, and alive programmable frequencies

Solfeggio frequencies, brain wave frequencies, clinical applications, and alive programmable frequencies

Jared Murray, CWC

Introduction

Solfeggio frequencies are a set of specific tones that are believed to have unique therapeutic properties. These frequencies are used in various healing practices to promote mental, emotional, and physical well-being. They are thought to correspond with specific brain wave frequencies, which can be harnessed to achieve different states of consciousness and therapeutic outcomes. This article explores the relationship between Solfeggio frequencies, brain wave frequencies, their clinical applications, and the innovative use of programmable frequency devices from Alive Innovations.

Solfeggio Frequencies and Brain Wave States

Solfeggio frequencies are a series of tones used in sound healing, with each frequency believed to provide different healing properties. They range from 396 Hz to 963 Hz and are thought to correspond to various brain wave states.

Solfeggio Frequencies and Brain Wave States
Chart: Solfeggio Frequencies and Their Correspondence with Brain Wave States
Solfeggio Frequency (Hz)
Brain Wave State
Brain Wave Characteristics
Potential Therapeutic Effects
References
396 Hz
Delta (0.5-4 Hz)
Deep sleep, restorative sleep
Reducing fear and guilt
Lane et al., 1998; Kramer et al., 2013
417 Hz
Theta (4-8 Hz)
Deep relaxation, meditation
Facilitating change, overcoming trauma
Watson et al., 2002; Peniston & Kulkosky
528 Hz
Alpha (8-14 Hz)
Relaxation, mental coordination
DNA repair, transformation
Entrainment Journal, 2005; Horowitz et al., 2013
639 Hz
Alpha (8-14 Hz)
Relaxation, mental coordination
Enhancing communicatio n, relationships
Lubar, 1997; Klimesch, 1999
741 Hz
Beta (14-30 Hz)
Active thinking, focus
Problemsolving, improving intuition
Monroe, 1993; Sterman, 1996
852 Hz
Gamma (30- 100 Hz)
Cognitive function, memory
Enhancing spiritual awareness
Tallon-Baudry et al., 1999; Lutz et al., 2004
Clinical Applications of Brain Wave Frequencies

Different brain wave states are associated with various cognitive and emotional functions, and inducing these states can have specific therapeutic benefits.

Delta Waves (0.5-4 Hz)
  • Characteristics: Deep sleep, restorative sleep
  • Therapeutic Effects: Healing and regeneration, reducing anxiety and stress
  • Applications: Insomnia, PTSD, chronic pain
Theta Waves (4-8 Hz)
  • Characteristics: Deep relaxation, meditation, creativity
  • Therapeutic Effects: : Accessing subconscious thoughts, enhancing creativity, reducing anxiety
  • Applications: Trauma therapy, addiction recovery, meditation practices
Alpha Waves (8-14 Hz)
  • Characteristics: Relaxation, mental coordination, stress reduction
  • Therapeutic Effects: Promoting relaxation, improving mood, reducing stress
  • Applications: Anxiety disorders, stress management, depression
Beta Waves (14-30 Hz)
  • Characteristics: Active thinking, focus, problem-solving
  • Therapeutic Effects: Enhancing concentration, improving alertness, reducing ADHD symptoms
  • Applications: ADHD, cognitive enhancement, learning disabilities
  • Gamma Waves (30-100 Hz)
  • Characteristics: Cognitive function, memory, information processing
  • Therapeutic Effects: Enhancing cognitive performance, improving memory, increasing focus
  • Applications: Schizophrenia, obsessive thoughts, cognitive disorders
Alive Innovations Programmable Frequencies

Alive Innovations offers programmable frequency devices that can be tailored to emit specific Solfeggio frequencies, thereby inducing desired brain wave states for therapeutic purposes. These devices offer a non-invasive and customizable approach to managing various mental health conditions.

Programmable Frequencies
Potential Therapeutic Applications
  • PTSD: Inducing theta waves to help with trauma recovery and emotional healing.
  • Anxiety and Depression: Inducing theta waves to help with trauma recovery and emotional healing.
  • Cognitive Dysfunction: Utilizing alpha waves to promote relaxation and improve mood.
  • Cognitive Dysfunction: Enhancing beta and gamma waves to improve focus, memory, and cognitive performance.
  • Insomnia: Increasing delta waves to promote deep and restorative sleep.
Conclusion

The integration of Solfeggio frequencies and brain wave frequency induction presents a promising avenue for therapeutic interventions. By leveraging the unique properties of these frequencies, programmable devices from Alive Innovations offer a novel approach to enhancing mental and emotional well-being. Continued research and clinical application will further elucidate the potential of these technologies in promoting holistic brain health.

Solfeggio frequencies and brain wave frequency
References
  1. Lane, J. D., Kasian, S. J., Owens, J. E., & Marsh, G. R. (1998). Binaural auditory beats affect vigilance performance and mood. Physiology & Behavior, 63(2), 249-252.
  2. Kramer, U. M., Rojo, N., Schule, R., Cunillera, T., Munte, T. F., & Rodriguez-Fornells, A. (2013). The oscillatory network of motor plasticity after piano learning in adults. NeuroImage, 74, 21-32.
  3. Watson, A., Gunasingh, T. G., & O’Connell, M. (2002). EEG entrainment with binaural beats: The patterning of cognitive and affective response in first year Psychology students. Australian Journal of Clinical Hypnotherapy and Hypnosis, 23(1), 30-39.
  4. Peniston, E. G., & Kulkosky, P. J. (1990). Alpha-theta brainwave training and betaendorphin levels in alcoholics. Alcoholism: Clinical and Experimental Research, 14(2), 271-279.
  5. Horowitz, S., & Horowitz, S. (2013). Sound Medicine: Music and the Brain. Alternative and Complementary Therapies, 19(1), 21-25.
  6. Entrainment Journal. (2005). The Healing Power of 528 Hz Frequency
  7. Lubar, J. F. (1997). Neocortical dynamics: Implications for understanding the role of neurofeedback and related techniques for the enhancement of attention. Applied Psychophysiology and Biofeedback, 22(2), 111-126.
  8. Klimesch, W. (1999). EEG alpha and theta oscillations reflect cognitive and memory performance: a review and analysis. Brain Research Reviews, 29(2-3), 169-195.
  9. Monroe, R. A. (1993). Journeys Out of the Body. Harmony.
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  12. Lutz, A., Greischar, L. L., Rawlings, N. B., Ricard, M., & Davidson, R. J. (2004). Long-term meditators self-induce high-amplitude gamma synchrony during mental practice. Proceedings of the National Academy of Sciences, 101(46), 16369-16373.
  13. Picower Institute for Learning and Memory. (2023). Cortical oscillations and neural synchrony in attention deficit hyperactivity disorder. Nature Neuroscience.
Medical Disclaimer:

Please note that this is medical information, None of the information presented here or on our social media is intended to service as medical, legal, or regulatory counsel. Users are encouraged to seek professional assistance and counsel if they are concerned about a specific medical, legal, or regulatory issue. None of the statements on this video have not been evaluated by the Food and Drug Administration. These products mentioned are not intended to diagnose, treat, cure, or prevent any disease. The information presented is intended for mainly professional usage and educational purposes and targeted for the US specifically; it is not intended to make claims about any products or services; for more information call 800-454- 1920/ info@aliveinnovations.com

The quantum cellular scan: a journey into rebalancing energy signatures and uncovering hidden or stealth infections. ovations micro blends

The quantum cellular scan: a journey into rebalancing energy signatures and uncovering hidden or stealth infections. ovations micro blends

Alive Innovations, Alive for Health

The Quantum Cellular Scan is an advanced diagnostic tool used in integrative medicine to assess the body’s energetic imbalances. This non-invasive method provides a comprehensive analysis of the body’s frequencies, offering insights into various health conditions, including latent or stealth infections. In this article, we will explore the testing process, the concept of rebalancing energy signatures, and the scientific basis for the memory of infections in the body’s frequencies.

Understanding the Quantum Cellular Scan

The Quantum Cellular Scan utilizes bioresonance technology to measure and analyze the body’s subtle energy fields. By emitting specific frequencies and recording the body’s response, the scan can detect discrepancies in the energetic signatures associated with different organs, tissues, and systems. These discrepancies can indicate imbalances or dysfunctions that may not yet manifest as clinical symptoms but can influence overall health and well-being.

Quantum Cellular Scan
The Testing Process
  1. Preparation: The client is seated comfortably, and sensors are placed on specific points of the body to detect bio-resonance signals.
  2. Scanning: : The device emits a series of frequencies corresponding to different parts of the body. The sensors record the body’s responses to these frequencies.
  3. Analysis: The recorded data is analyzed to identify any deviations from the optimal frequency patterns. These deviations are interpreted to understand the underlying imbalances or potential health issues.
  4. Report: A detailed report is generated, highlighting areas of concern and suggesting possible interventions to restore balance.
Rebalancing the Energy Signature

Once imbalances are identified, the next step is to rebalance the body’s energy signature. This process involves using specific electro frequencies to harmonize the body’s bio-resonance patterns. Techniques such as biofeedback, frequency therapy, and nutritional support are commonly employed to restore optimal energy flow.

Rebalancing the Energy Signature
Stealth Infection Memory of Infection: A Frequency Perspective

A fascinating aspect of the Quantum Cellular Scan is its ability to detect frequencies that may indicate the presence of latent or stealth infections. These infections, often undetectable by conventional methods, can leave an energetic imprint on the body’s tissues. This concept is akin to the “memory of water” theory proposed by Dr. Michel Montagnier.

Rebalancing the Energy Signature

Dr. Montagnier’s research suggests that water can retain the informational imprint of substances that were once dissolved in it, even after they are removed. Similarly, the body’s water matrix and structure may retain the energetic signatures of past infections. These signatures can persist long after the active infection has been resolved, influencing the body’s energy balance and potentially leading to subclinical manifestations

Water matrix
Clinical Manifestations in Integrative Medicine

Integrative medicine recognizes the importance of addressing these latent infections to achieve health. For example:

  • Dental and Sinus Focus of Infection: Latent infections in the dental or sinus regions can manifest as chronic health issues. The Quantum Cellular Scan can detect these hidden infections by identifying their energetic signatures, allowing for targeted interventions such as antimicrobial therapies, detoxification, and supportive nutrition.
  • Subclinical Syndromes: Stealth infections can contribute to subclinical syndromes, where the patient experiences vague symptoms that are not easily diagnosed through conventional methods. By rebalancing the energy signature, integrative practitioners can address the root cause of these symptoms.
Scientific Basis and References

The concept of energy imbalances and the memory of infections in the body’s frequencies is supported by emerging scientific research. Dr. Montagnier’s ground breaking work on the memory of water provides a plausible mechanism for how these energetic signatures can persist in the body. Additionally, studies on bio-resonance and frequency therapy have shown promising results in detecting and addressing hidden infections and imbalances.

For further reading and reference, consider the following sources:
  1. Montagnier, L., et al. (2009). Electromagnetic signals are produced by aqueous nanostructures derived from bacterial DNA sequences. Interdisciplinary Sciences: Computational Life Sciences, 1(2), 81-90.
  2. Gerber, R. (2001). Vibrational Medicine: New Choices for Healing Ourselves. Bear & Company.
  3. Rubik, B. (2002). The biofield hypothesis: Its biophysical basis and role in medicine. Journal of Alternative and Complementary Medicine, 8(6), 703-717.
Conclusion

The Quantum Cellular Scan offers a unique and insightful approach to understanding and rebalancing the body’s energy signatures. By detecting the memory of infections and/or addressing latent imbalances, integrative practitioners can provide comprehensive care that goes beyond conventional diagnostics. As research in this field continues to evolve, the potential for bio-resonance technology to enhance our understanding of health and disease is immense.

Medical Disclaimer:

: Please note that this is medical information, None of the information presented here or on our social media is intended to service as medical, legal, or regulatory counsel. Users are encouraged to seek professional assistance and counsel if they are concerned about a specific medical, legal, or regulatory issue. None of the statements on this video have not been evaluated by the Food and Drug Administration. These products mentioned are not intended to diagnose, treat, cure, or prevent any disease. The information presented is intended for mainly professional usage and educational purposes and targeted for the US specifically; it is not intended to make claims about any products or services; for more information call 800-454- 1920/ info@aliveinnovations.com