This RF Safe article argues that biological effects from radiofrequency and pulsed electromagnetic fields can be interpreted through two complementary layers: Maxwell–Wagner interfacial polarization (as a direct electrodynamic mechanism at cell membranes) and an “S4–Mito-Spin” framework (as an upstream susceptibility model tied to voltage-sensor density, mitochondrial coupling, and antioxidant buffering). It suggests these mechanisms could converge on outcomes such as altered red-blood-cell stability, blood rheology, membrane deformation, and—at higher intensities—electroporation or hemolysis. The piece is presented as a mechanistic synthesis rather than reporting new experimental results, and it frames potential vulnerability to pulsed/non-native exposures as context-dependent.

This PubMed-listed in vitro study tested whether 1800 MHz RF-EMF exposure can modify chemically induced DNA damage in mouse embryonic fibroblasts under standardized, non-thermal conditions. The authors report RF-EMF alone did not produce detectable DNA damage and did not significantly increase damage from hydrogen peroxide, 4-nitroquinoline-1-oxide, or cadmium. However, co-exposure with hexavalent chromium (Cr(VI)) was reported to synergistically increase DNA damage in the comet assay, which the authors interpret as possible selective exacerbation of Cr(VI)-induced genotoxicity requiring further investigation.

RF Safe argues that Media Bias/Fact Check (MBFC) downgraded RF Safe partly by citing an FDA webpage stating typical RF exposure is not supported by current evidence as a health risk, but that the cited FDA page now redirects to a general “Cell Phones” landing page. The post claims other historically cited FDA consumer pages also redirect and that the strongest reassurance language is now mainly accessible via archives. It further cites Reuters reporting that FDA removed outdated webpages about cellphone safety alongside HHS launching a new study, and contends MBFC should update its rationale and links.

This RF Safe commentary argues that if HHS and FDA pursue a “reset” on cellphone radiation policy, they should fund mechanistic, predictive biology rather than relying on literature summaries or general safety reassurances. It cites the NTP rat bioassays and a WHO-commissioned animal cancer systematic review (Mevissen et al., 2025) as motivation, emphasizing reported tissue-selective findings and non-monotonic dose patterns. The post proposes a mechanistic framework (“S4–Mito–Spin”) and calls for research to map boundary conditions across tissues and exposure parameters to inform standards beyond SAR/thermal assumptions.

RF Safe promotes its QuantaCase (also called TruthCase) as a leading “anti-radiation” phone case for 2026, emphasizing a directional shielding design intended to deflect RF energy away from the body. The article argues the product aligns with consumer-safety guidance such as keeping phones away from the body and using hands-free modes, and it claims RF Safe’s earlier advocacy influenced FTC/FCC warnings about ineffective or counterproductive shielding products. It cites comparisons, user reviews, and an “independent” 2017 TV review as support, but presents limited verifiable technical detail in the excerpt.

RF Safe argues that “no effect” findings in some RF exposure studies should be interpreted as meaningful negative controls rather than as evidence that RF has no biological effects. The post presents RF Safe’s “S4–Mito–Spin” framework, claiming certain skin cell types (fibroblasts and keratinocytes) are predicted to be relatively resistant to non-thermal RF effects, so null results in these cells can be consistent with the model. It cites in-vitro studies at 3.5 GHz (5G-modulated) reporting no changes in ROS measures, stress responses, or UV-B DNA repair kinetics under specified SAR conditions, and frames these nulls as boundary conditions rather than a general safety conclusion.

RF Safe publishes a commentary disputing Media Bias Fact Check’s (MBFC) labeling of RF Safe as “pseudoscience” with “mixed factual reporting” and “low credibility.” The post argues MBFC mischaracterized RF Safe’s content as overstating evidence about cell phones and health, claiming RF Safe generally uses cautious, study-referencing language (e.g., “associations,” “potential risks”) and avoids asserting direct human causation. It also points to RF Safe disclaimers that the site is educational and not medical advice, and highlights its research library linking to primary studies such as NTP and Ramazzini animal findings.

This PubMed-listed paper argues that the U.S. regulatory framework for radiofrequency radiation (RFR) from wireless technologies is outdated, lacks adequate oversight and enforcement, and has not been meaningfully updated since 1996. It contends that FCC exposure limits focus on short-term, high-intensity effects and do not address long-term, low-intensity exposures, with insufficient safeguards for children, pregnancy, and other vulnerable groups. The authors also discuss alleged regulatory capture, gaps in monitoring and compliance, and propose reforms including independent research, updated safety limits, and stronger pre- and post-market surveillance.

RF Safe criticizes Media Bias Fact Check (MBFC) for labeling RF Safe as “pseudoscience” with “mixed factual reporting” and “low credibility,” arguing MBFC’s entry contains factual errors and misrepresentations. The post says RF Safe does not claim RF radiation definitively causes human disease, but instead presents precautionary interpretations of peer-reviewed studies and proposed non-thermal mechanisms. It also alleges MBFC made specific, checkable mistakes about study-linking practices and site ownership/funding, and failed to correct them after rebuttals.

RF Safe publishes a rebuttal to Media Bias Fact Check (MBFC) after MBFC labeled RF Safe as “pseudoscience” with “mixed factual reporting” and “low credibility.” The article argues MBFC made factual errors about RF Safe’s research links and ownership/funding, and says MBFC has not corrected the entry despite requests. RF Safe also defends its framing of non-thermal RF/EMF effects as precautionary and grounded in peer-reviewed literature, while criticizing what it characterizes as superficial fact-checking.

This RF Safe commentary argues that U.S. RF exposure protections remain anchored to “thermal-only” assumptions from the 1990s despite what it describes as newer WHO-commissioned systematic reviews elevating certain animal cancer endpoints and a male fertility endpoint to “high certainty.” It contrasts these claims with a WHO-commissioned review of human observational studies that reportedly found mobile-phone RF exposure is likely not associated with increased risk of several head/brain tumors, arguing that this is often overgeneralized in public messaging. The piece calls for “prudent avoidance,” updates to FCC rules, and highlights legal and policy constraints such as federal preemption under the Telecommunications Act and a 2021 D.C. Circuit decision criticizing the FCC’s rationale for retaining its RF limits without adequate explanation.

This animal experiment assessed GSM-modulated 3.5 GHz RF exposure in male Wistar rats and reported hormonal, oxidative, and histological changes consistent with testicular impairment. RF exposure was associated with lower testosterone, LH, and FSH, higher oxidative stress (increased MDA and TOS), and degenerative testicular histology. Coenzyme Q10 supplementation partially mitigated several reported changes. The authors caution against generalizing these results to FR1 5G NR signals and call for further research.

This in vitro study examined strictly non-thermal, GSM-like 3.5 GHz RF-EMF exposure in cultured mouse dorsal root ganglion neurons for 1–24 hours. The authors report time-dependent reductions in cell viability alongside increased ROS and changes consistent with mitochondria-mediated apoptosis (e.g., Bax/caspase-3 up, cytochrome c release, Bcl-2 down) and increased p75NTR. They conclude these findings provide mechanistic evidence of peripheral neuronal vulnerability to mid-band RF exposure and call for further in vivo research.

This in vitro study tested whether 1800 MHz RF-EMF modifies chemically induced DNA damage in mouse embryonic fibroblasts under non-thermal exposure conditions. RF-EMF alone did not produce detectable DNA damage and did not significantly enhance damage from hydrogen peroxide, 4NQO, or cadmium. In contrast, co-exposure with hexavalent chromium (Cr(VI)) was reported to synergistically increase DNA damage, suggesting a selective co-genotoxic interaction under specific chemical conditions.

This study reports measurements of electric field intensity (E) and magnetic flux density (B) from electric vehicles (inside driver/passenger seats during driving) and EV supply equipment (near chargers during charging) up to 400 kHz in and around Chennai. E and B inside EVs and E around EVSEs were reported to be within ICNIRP/IEEE guideline limits. However, B around certain EVSE positions reportedly exceeded a general public threshold (~200 T), and a preliminary FEM analysis suggested relatively higher fields at charging infrastructure. The authors call for further research on long-term health impacts and recommend policy actions to mitigate exposure.

RF Safe argues that non-native electromagnetic fields (EMFs) can affect biology through timing and redox mechanisms even without tissue heating, framing this as a challenge to common safety narratives focused on thermal effects. The post links circadian disruption (citing a 2025 Frontiers in Psychiatry paper on ADHD and circadian phase delay) to broader vulnerability of biological timing systems, and proposes an “S4–Mito–Spin” framework involving ion-channel timing noise, mitochondrial oxidative stress amplification, and radical-pair/spin chemistry. It also cites a 2018 PLOS Biology study as mechanistic support for cryptochrome-dependent ROS changes under weak pulsed EMF exposure, while presenting these points as converging evidence rather than definitive proof of harm in real-world exposures.

RF Safe promotes QuantaCase (also marketed as TruthCase) as an “anti-radiation” phone case designed to deflect RF energy away from the user while maintaining phone performance. The article argues that non-thermal biological effects can occur below current exposure guidelines and cites multiple reviews and reports to support a precautionary approach, while stating it does not directly extrapolate these findings to proven human harms. It also criticizes current RF standards and regulators, references the 2021 D.C. Circuit remand of the FCC’s RF decision, and advocates exposure-reduction strategies such as Li‑Fi and consumer action.

RF Safe presents “TruthCase™ · Clean Ether Action Hub” as a combined product-and-policy hub arguing that evidence from multiple RF health research lines supports harm occurring below current exposure limits. It promotes a proposed “S4–Mito–Spin / IFO‑VGIC” framework and a “density-gated” vulnerability map, and calls for policy actions such as changes to Section 704 and enforcement via FDA/FTC. The page frames regulatory “capture/inertia” as a key reason current limits persist, while positioning its view as a “respectable minority” in 2025.

This RF Safe article argues that the organization’s EMF safety advocacy should not be dismissed as “biased” or “commercially motivated,” framing its work as rooted in its founder’s personal experience and long-term activism. It recounts founder John Coates’ claim that prenatal RF exposure contributed to his infant daughter’s neural tube defect, and presents RF Safe as combining advocacy, scientific synthesis, and product development. The piece also claims RF Safe’s antenna work helped prompt a 2003 FCC rule change recognizing directional antenna approaches to reduce energy toward users while maintaining performance.

An RF Safe article argues that, as of 2025, evidence is “decisive” that man-made radiofrequency (RF) fields can cause cancer and other biological harm, and that non-thermal mechanisms are now established. It cites animal studies (including NTP and Ramazzini), a 2025 WHO-commissioned systematic review (as described by the author), and proposed mechanisms involving voltage-gated ion channels, oxidative stress, and radical-pair/spin chemistry. The piece calls for updated safety standards that consider modulation and tissue vulnerability, while stating it is “not a call for panic.”

This RF Safe article discusses rouleaux formation (reversible red blood cell stacking) and proposes a speculative mechanism by which weak magnetic fields might influence red blood cell surface charge (zeta potential) via spin chemistry in heme-related radical-pair processes. The piece frames the idea as a mechanistic “what if?” rather than a direct claim that everyday phone use causes blood clotting, and it leans on general concepts from hematology and radical-pair magnetosensitivity (e.g., cryptochrome in animals). No new experimental data are presented in the provided text; the argument is largely theoretical and interpretive.