A little light, every day.
Two lights — one for the patient, one for the family caring for them.
A companion for children with rare epilepsy and cognitive differences — and a continuous record of what matters, between visits.
Follow the journeyA child with rare epilepsy sees a neurologist once or twice a year. Between those visits, families navigate almost entirely without data.
It is not a failure of care. There is simply no platform yet built around the individual patient — capturing their unique cognitive and neurological profile over time, in real life, not in a clinic.
A six-year-old and a fifteen-year-old should not be looking at the same screen. The cognitive measurement underneath is identical — validated, WISC-aligned, longitudinal. The way it shows up is radically different.
Twelve weeks instead of one afternoon. A clear baseline for this patient — not a comparison against averages that may never have applied to them.
The data vacuum is most acute in rare genetic epilepsies. We start there — because the need is sharpest, and a small, focused product can make an immediate difference. The architecture generalises.
No dates. No promises. Stage-gated by what we learn and what funds. Every step is shaped by conversations with families — not by a product roadmap written in a vacuum.
No dates yet · Stage-gated by what we learn and what funds
2lux is an early-stage research project. If something here resonates — as a family, a clinician, or a builder — we'd like to stay in touch.
No spam · Updates only when there is something real to share