HUMAN CELL & EMF STUDY –> Indep Lab shows cellular effects of EMFs can be nullified.

See the first and only one in history, a study by Dr Mazvita Maziveyi.  Until now, nobody has shown an actual solution for what happens in human cells when exposed to EMF radiation.  And this solution has a perfect Probability Value (in other words…it really works!)…

 

Reversal of EMF-Induced Calcium Dysregulation in Human Cells Using Remediation Devices

 

Maziveyi, M.

 

Abstract

 

Exposure to electromagnetic fields (EMFs), particularly from ubiquitous sources such as Wi-Fi

routers, has been shown to alter intracellular calcium levels via voltage-gated calcium channels

(VGCCs). This study evaluated the effects of EMF exposure on calcium levels in four human

cell lines—skin (BJ), liver (THLE-2), breast (MCF10A), and colon (HCEC)—and investigated

whether earth-based EMF remediation products from EMF Solutions could reverse these

changes. Using fluorescence-based calcium assays, calcium levels were assessed under three

conditions: control (no added EMFs), EMF exposure, and EMF exposure with remediation. EMF

exposure caused significant dysregulation of intracellular calcium levels in skin and breast cells.

The use of a Device Chip and XL Home Harmonizer Box normalized these alterations with a

significance level of p < 0.0001. No significant calcium fluctuations were observed in liver or

colon cells. These findings suggest that specific EMF remediation strategies may offer

protective benefits for cell types sensitive to EMF-induced calcium dysregulation.

 

 

Introduction

 

Electromagnetic fields (EMFs) are invisible areas of energy commonly associated with the use

of electrical power and various forms of natural and man-made lighting and communication

devices (EPA, 2024). EMFs exist across a broad spectrum, ranging from extremely low

frequency (ELF) radiation—such as that emitted by power lines—to higher frequency

radiofrequency (RF) radiation used in wireless communications, including Wi-Fi routers, mobile

phones, and Bluetooth devices (National Institute of Environmental Health Sciences [NIEHS],

2020). Unlike ionizing radiation (e.g., X-rays, gamma rays), which has enough energy to remove

tightly bound electrons from atoms, non-ionizing radiation such as EMFs is considered less

harmful because it lacks this ionizing capacity (World Health Organization [WHO], 2022).

 

However, despite being classified as non-ionizing, EMFs are increasingly implicated in biological

effects that cannot be solely explained by traditional thermal or energetic models. Numerous

studies over the past two decades have reported biological changes associated with EMF

exposure, including oxidative stress, changes in DNA integrity, altered gene expression,

reduced sperm quality, and cellular signaling disruptions (Belpomme et al., 2018; Yakymenko et

al., 2016; BioInitiative Report, 2012). The World Health Organization’s International Agency for

Research on Cancer (IARC) has classified radiofrequency electromagnetic fields as “possibly

carcinogenic to humans” (Group 2B), based on increased risk for glioma, a malignant type of

brain cancer, associated with wireless phone use (IARC, 2011).

 

One of the most compelling mechanisms proposed to explain the non-thermal biological effects

of EMFs involves the activation of voltage-gated calcium channels (VGCCs). VGCCs are

integral membrane proteins that allow the passage of calcium ions (Ca²⁺) into cells in response

to changes in membrane potential. These channels are crucial in regulating numerous

physiological processes including neurotransmission, hormone secretion, gene expression, and

cellular proliferation (Berridge, 2012).

 

Dr. Martin Pall has been a leading voice in this area, proposing that EMFs—particularly at low

frequencies—exert their effects by directly stimulating VGCCs, causing an abnormal influx of

calcium into the cell (Pall, 2013). His theory is supported by pharmacological studies in which

VGCC blockers significantly reduced or eliminated EMF-induced biological changes, including

calcium influx, oxidative stress, and DNA breaks (Pall, 2015). Among the VGCC subtypes,

L-type channels have shown the greatest susceptibility to EMF-induced activation, especially in

electrically excitable cells such as neurons and muscle tissue. Other subtypes, including N-type,

P/Q-type, and T-type VGCCs, have also been implicated, with some exhibiting decreased

intracellular calcium in response to EMF exposure, depending on the cellular context (Pall,

2013).

 

This calcium dysregulation may trigger a cascade of downstream effects, such as increased

production of reactive oxygen species (ROS), nitric oxide signaling abnormalities, mitochondrial

dysfunction, and alterations in transcriptional activity (Pall, 2015; Yakymenko et al., 2016).

These molecular disruptions may underlie the diverse health complaints reported by individuals

exposed to high levels of EMFs, ranging from headaches and sleep disturbances to more

chronic issues like infertility and neurodegeneration (Belpomme et al., 2018).

 

Despite accumulating evidence, the topic of EMF exposure remains controversial. Skeptics

argue that many reported effects stem from poorly controlled studies or are the result of nocebo

effects (i.e., negative health outcomes induced by the belief that EMFs are harmful) (Eltiti et al.,

2018; Schmidt et al., 2019; de Vocht, 2017; Dieudonné, 2016). Others point to a lack of

consistent epidemiological evidence linking EMFs with adverse health outcomes. Nevertheless,

the rapid global expansion of EMF-emitting devices has prompted increasing public concern

and a call for more robust studies, particularly those that investigate underlying biological

mechanisms and evaluate possible methods of remediation (WHO, 2022).

 

In this context, EMF Solutions has developed products designed to mitigate the biological

impact of EMFs using materials and designs said to harmonize electromagnetic frequencies at a

subatomic level. These include the Device Chip, which is affixed to power cords, and the XL

Home Harmonizer Box, which is designed to neutralize ambient EMFs within a broader

environment. According to EMF Solutions, EMFs are composed of photons traveling at the

speed of light. When these photons are absorbed by solid materials, they can induce both

thermal effects and what the company refers to as “subatomic chaos”—a phenomenon where

particles enter an excited state that disrupts normal subatomic organization. This subatomic

chaos is said to conduct especially well through metals and may be the true cause of

voltage-gated calcium channel (VGCC) malfunction, rather than the EMFs themselves. EMF

Solutions posits that its products address this subatomic disruption directly—not by blocking

EMFs, but by using natural materials to create quantum coherence and restore order at the

subatomic level.

 

The XL Home Harmonizer Box was selected specifically to address not only the EMF radiation

within the incubator but also ambient EMFs from external sources such as nearby cell towers,

SCADA poles, Wi-Fi routers, and other infrastructure in the vicinity that could influence the

experimental environment. The present study evaluates the effectiveness of these remediation

tools in restoring normal calcium signaling in human cells exposed to Wi-Fi-generated EMFs.

We hypothesized that if EMFs dysregulate calcium levels via VGCC activation, then effective

remediation would reverse this disruption and normalize intracellular calcium concentrations.

 

 

 

Methods 

 

Cell Culture Conditions

 

Four human cell lines were used in this study: BJ (human foreskin fibroblasts), MCF10A

(non-tumorigenic mammary epithelial cells), THLE-2 (liver epithelial cells), and HCEC (human

colon epithelial cells). Each cell line was cultured in its optimal growth medium to ensure healthy

and consistent proliferation during experimentation.

 

BJ cells are skin fibroblasts taken from foreskin of a neonatal male and were maintained in

Eagle’s Minimum Essential Medium (EMEM) supplemented with 10% fetal bovine serum (FBS)

and 1% penicillin-streptomycin to support fibroblast growth and prevent bacterial contamination.

MCF10A breast epithelial cells were cultured in a 1:1 mixture of Dulbecco’s Modified Eagle

Medium and Ham’s F12 (DMEM/F12), supplemented with 5% horse serum, 20 ng/mL epidermal

growth factor (EGF), 10 µg/mL insulin, 0.5 µg/mL hydrocortisone, 100 ng/mL cholera toxin, and

1% penicillin-streptomycin. THLE-2 liver epithelial cells were cultured in Bronchial Epithelial Cell

Growth Medium (BEGM), based on LHC-9 or BEGM BulletKit formulations, with additional

supplementation of 5 ng/mL EGF and 70 ng/mL phosphoethanolamine, as per ATCC guidelines.

This medium is serum-free and designed to support the growth of non-transformed liver

epithelial cells.

 

HCEC colon epithelial cells were cultured in DMEM/F12 supplemented with 10% FBS, 5 µg/mL

insulin, 5 µg/mL transferrin, and 10 ng/mL EGF. Depending on the cell line variant, additional

supplements such as hydrocortisone or cholera toxin were included as needed. All cells were

incubated at 37°C in a humidified atmosphere containing 5% CO₂.

 

Experimental Design

 

Three experimental conditions were applied to each cell type (Figure 1):

 

1. Test #1 – Control (No Added EMFs):

Cells incubated without additional EMF exposure.

 

2. Test #2 – EMF Exposure:

Wi-Fi router placed 12 inches from cell culture trays for 24 hours.

 

3. Test #3 – EMF + Remediation:

Same EMF exposure as Test #2, with two remediation devices:

 

○ Device Chip: Attached to the router’s power cord.

 

○ XL Home Harmonizer Box: Placed adjacent to the incubator.

Calcium Quantification Assay

 

Intracellular calcium levels were measured using a fluorometric calcium quantification assay

based on a red-fluorescent calcium-binding probe. This method is designed for sensitive

detection of calcium ions in in vitro samples and is compatible with cells cultured directly in

microplate wells.

 

For each condition (control, EMF-exposed, and EMF-exposed with remediation), cells were

cultured directly in a black-walled, clear-bottom 96-well microplate. Following incubation under

the respective experimental conditions, the cells were lysed in situ to produce solution-based

samples suitable for calcium quantification. A reaction mix containing the calcium-sensitive

fluorescent probe was then added directly to the wells. The plate was incubated at room

temperature for 30 minutes, and fluorescence intensity was measured using a microplate reader

set to an excitation/emission wavelength of approximately 540/590 nm.

 

This assay offers a broad dynamic range (30 µM to 1 mM) and can detect calcium

concentrations as low as 0.03 mM. The procedure does not require separation or wash steps

and was completed within 30 minutes. All samples were analyzed in octuplicate, and mean

fluorescence values were used for comparing calcium levels across conditions.

 

 

Statistical Analysis

 

One-way ANOVA followed by Tukey’s post hoc test was used to compare calcium levels across

groups. Significance was set at p < 0.05.

 

 

 

Results

 

Exposure to electromagnetic fields (EMFs) from a Wi-Fi router significantly affected intracellular

calcium levels in some cell types, but not in others, as shown in Figure 2.

In skin (BJ) cells, exposure to EMFs resulted in a significant influx of calcium into the cells,

indicating that EMFs can disrupt calcium homeostasis in skin/fibroblast cells. The application of

the remediation techniques—specifically the Device Chip and Home Harmonizer—effectively

restored intracellular calcium levels to baseline, suggesting that these products can reverse

EMF-induced calcium dysregulation. The reversal was highly statistically significant, with a

p-value of ****p < 0.0001, indicating the highest confidence in the data (Figure 2A).

 

In breast (MCF10A) cells, EMF exposure caused a significant efflux of calcium, lowering

intracellular calcium levels compared to the control group. After the application of the same

remediation products, intracellular calcium levels were significantly increased, although the

levels did not fully return to baseline values. Despite this partial restoration, the statistical

significance of the increase was extremely high, with a p-value of ****p < 0.0001, indicating the

highest confidence in the effect of the remediation strategy in reversing the EMF-induced

calcium imbalance (Figure 2B).

 

In liver (THLE-2) cells, EMF exposure did not cause any significant change in intracellular

calcium levels compared to the control group, indicating that liver cells may be less sensitive to

the effects of EMFs on calcium homeostasis. Similarly, the application of the remediation

products (Device Chip and Home Harmonizer) did not significantly alter calcium levels in these

cells. The p-value for the comparison between the different conditions was p > 0.05, indicating

no statistically significant difference in calcium levels (Figure 2C).

 

Similarly, colon (HCEC) cells showed no significant changes in intracellular calcium levels due

to EMF exposure. Remediation did not significantly affect calcium levels in these cells either,

with a p > 0.05, indicating no significant difference across the conditions (Figure 2D).

 

These results, illustrated in Figure 2, suggest that the impact of EMFs on calcium homeostasis

is cell type-specific. Skin and breast cells were notably affected by EMF exposure and showed

significant improvements with the application of remediation techniques, while liver and colon

cells did not demonstrate significant changes, either with EMF exposure or with the remediation

strategies.

 

 

Discussion

 

This study confirms that electromagnetic fields (EMFs) emitted from common household

devices—specifically Wi-Fi routers—disrupt calcium homeostasis in human cells. Notably, we

observed a cell-type-specific directional shift in calcium concentration: an increase in skin cells

and a decrease in breast epithelial cells. This differential response supports the hypothesis that

VGCC (voltage-gated calcium channel) subtypes and expression profiles vary between cell

types and mediate distinct susceptibilities to EMF exposure.

 

To investigate potential remediation, we evaluated two products developed by EMF Solutions:

the Device Chip and the XL Home Harmonizer Box. According to EMF Solutions, EMFs consist

of photons traveling at the speed of light. Upon interaction with solid materials, these photons

are thought to induce not only thermal effects but also what the company terms subatomic

chaos—a phenomenon in which particles enter excited states, disrupting subatomic structure

and coherence. This subatomic chaos is said to propagate especially efficiently through

conductive materials like metal. EMF Solutions suggests that this secondary phenomenon—not

the EMFs themselves—triggers VGCC dysfunction, leading to abnormal calcium signaling. The

Device Chip and Harmonizer are not designed to block EMFs but instead aim to restore

quantum coherence through natural materials that stabilize subatomic organization.

 

The XL Home Harmonizer Box was selected for its capacity to address both local and ambient

EMF radiation, extending beyond the incubator environment to include external sources such as

cell towers, SCADA (Supervisory Control and Data Acquisition) infrastructure, neighboring Wi-Fi

routers, and other forms of pervasive electromagnetic pollution. In combination with the Device

Chip, which was affixed to the power cords of equipment within the experimental setup, these

tools were hypothesized to counteract EMF-induced biological effects at the subatomic level.

 

Our findings support this hypothesis. When applied, both remediation devices effectively

reversed the calcium imbalances observed in skin and breast epithelial cells. This reversal

suggests that the products may alter the electromagnetic environment in a way that reduces

inappropriate VGCC activation or inhibition. Interestingly, liver and colon epithelial cells—both of

which are located deeper within the body and typically shielded by overlying tissue—did not

exhibit significant calcium fluctuations in response to EMF exposure or remediation. This may

indicate either limited EMF penetration in vivo or different VGCC compositions that confer

resistance to EMF-induced effects.

 

These results align with a growing body of evidence indicating that EMFs, though non-ionizing,

can exert significant biological influence, particularly through disruption of calcium signaling

pathways. More importantly, our data suggest that strategic mitigation using

coherent-energy-based technologies may provide a viable method to restore homeostasis in

EMF-sensitive cell types. While further research is needed to confirm these findings in vivo and

to dissect the precise molecular interactions involved, this study offers preliminary support for

the potential of subatomic-level EMF remediation.

 

 

Conclusion

 

Exposure to EMFs from a Wi-Fi router caused significant calcium dysregulation in skin-exposed

human cells. Earth-based EMF remediation tools from EMF Solutions successfully reversed

these disruptions. These findings highlight the need for further investigation into EMF mitigation

and its potential role in promoting cellular health.

 

 

 

 

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