your symptoms are real.
science confirms it.
Headaches, chronic fatigue, sleep disturbances near screens or mobile towers? The DEMETER study (INSERM 2025) confirms a measurable cellular defect in 100% of electrosensitive individuals tested. Our programme targets these mechanisms directly through photobiomodulation and targeted nutritional support.
electrosensitivity is real:
science confirms it
For years, people suffering from electrohypersensitivity (EHS) were told their symptoms were psychosomatic. A study published in 2025 changes everything.
Dr Nicolas Foray's team at INSERM Lyon conducted the DEMETER study on 26 self-reported EHS individuals. The researchers took skin cell samples (fibroblasts) and analysed their function at the molecular level.
The findings are unequivocal: 100% of those tested showed a defect in the RIANS cellular mechanism (Radiation-Induced ATM Nucleoshuttling). This is not a matter of perception. It is a measurable biological reality.
why your cells
don't repair as well
Our cells are under constant assault: radiation, oxidative stress, toxins. The ATM protein (Ataxia Telangiectasia Mutated) plays a central role in DNA repair. When a break occurs, ATM migrates rapidly to the cell nucleus to coordinate the repair process.
In electrosensitive individuals, this migration is delayed. Their cells are slower to detect damage and less efficient at repairing it. It is not that EMFs cause more damage — it is that the capacity to handle cellular stress is compromised.
This discovery explains why EHS symptoms are not limited to electromagnetic fields. Many sufferers also report heightened sensitivity to chemicals, light, noise, or disproportionate fatigue from everyday stress.
two profiles,
two risks
The DEMETER study identified two subgroups:
Low Background, Highly Responsive
Cells show little baseline damage but react strongly to stress.
High Background, Lowly Responsive
Cells carry high levels of baseline damage and respond weakly to further aggression.
Both profiles call for the same therapeutic approach: optimising the cellular repair mechanisms.
photobiomodulation and targeted nutrition
Avoiding EMF sources (switching off the router, using airplane mode) helps, but it doesn't address the underlying problem. Our approach targets the faulty cellular mechanisms directly.
Kickstarting cellular repair
Red light (660 nm) applied to the wrists. This transcutaneous blood irradiation technique, used for decades in physical medicine, directly stimulates cellular activity and repair pathways including the ATM protein.
- Increased ATP production (cellular energy)
- Activation of repair pathways including ATM protein
- Restoration of membrane ionic balance
- Stimulation of antioxidant defences (Nrf2 pathway)
Supplying the repair cofactors
Each supplement targets a specific step in the cellular repair process. Introduction is gradual, tailored to each patient's tolerance — people with EHS are often sensitive to many substances.
- Resveratrol + astaxanthin — activate SIRT1, protect membranes
- GlyNAC — glutathione precursors
- Curcumin — anti-inflammatory, potentiated by laser
- Magnesium, zinc, B vitamins — enzymatic repair cofactors
three clear steps
Initial assessment
Thorough medical history, identification of aggravating factors. Targeted blood panel: inflammation markers (CRPus, oxidised LDL), membrane fatty acid profile, thyroid function, iodine and vitamin D status. These results allow us to tailor the protocol.
Intensive programme — 2 weeks
Daily sessions at the centre: photobiomodulation (20 min), vagal stimulation if needed, TMJ physiotherapy if indicated. Most patients report improved energy and sleep within the first few days.
Home consolidation
Continued supplement protocol and dietary adjustments. Reduction of refined carbohydrates and fructose. Follow-up blood panel at 8–12 weeks to assess progress and adjust.
what people ask us
reimbursement
Covered by basic health insurance (LAMal) as physiotherapy
Prescribed by the doctor, covered by LAMal
At your own expense
full
transparency
We do not claim to 'cure' electrosensitivity. The ATM transit defect appears to be a constitutional trait. What we offer is optimising the compensatory mechanisms to reduce the impact on your quality of life.
We do not promise miraculous results. Each person responds differently. Some notice rapid improvement; others experience a more gradual change.
We are not asking you to take our word for it. We invite you to measure: your symptoms before and after, your biological markers, your quality of life.
this programme is
right for you if
- You experience symptoms consistent with electrosensitivity (headaches, fatigue, cognitive difficulties near electronic devices)
- You have already tried removing EMF sources without sufficient improvement
- You want an approach grounded in the understanding of biological mechanisms
- You are ready to commit to a structured programme lasting several weeks
- Sonzogni L, et al. Skin Fibroblasts from Individuals Self-Diagnosed as Electrosensitive Reveal Two Distinct Subsets with Delayed Nucleoshuttling of the ATM Protein in Common. Int J Mol Sci. 2025;26(10):4792. DOI
- Calabrese EJ, Kozumbo WJ. The hormetic dose-response mechanism: Nrf2 activation. Pharmacol Res. 2021;167:105526. DOI
real solutions exist —
and they're measurable
Book an initial assessment. 30 minutes with our advisor to evaluate your situation. No commitment.
1204 Genève