Support, never replace
MyRemD is a companion to clinicians, not a substitute. Diagnosis and treatment remain with licensed professionals.
Help shape the future of evidence-informed sleep health. MyRemD is collaborating with clinicians, researchers, healthcare organizations, and innovators to build technology that improves patient outcomes while supporting — not replacing — healthcare professionals.
MyRemD sits between consumer wellness and clinical practice — bringing longitudinal context to the exam room and clinical rigor to the everyday.
Patient engagement between visits, not only at intake.
Built on CBT-I and circadian evidence, reviewed by clinicians.
Longitudinal sleep intelligence you can actually use.
For your time, your patients, and your clinical judgment.
MyRemD is a companion to clinicians, not a substitute. Diagnosis and treatment remain with licensed professionals.
Behavioral sleep medicine and circadian science form the foundation of every recommendation surface.
Sleep is a pattern, not a night. We build for months and years of context, not single-session snapshots.
Consent, privacy and clarity are non-negotiable. Data belongs to the patient.
MyRemD is built on established behavioral sleep medicine — cognitive behavioral therapy for insomnia (CBT-I), stimulus control, sleep restriction and circadian rhythm science.
We do not overstate. Where evidence is emerging, we say so. Where a feature is planned, we mark it. Where a claim would require regulatory clearance we do not yet hold, we don't make the claim.
Our validation roadmap includes real-world evidence studies, clinician-in-the-loop evaluations, and peer-reviewed publications with partner institutions.
Founding clinical voices guiding product direction, safety and scope.
Structured review of flows, language and clinical guardrails.
Longitudinal, consented studies in chronobiology and CBT-I.
Introduce MyRemD to a defined patient panel with measurable endpoints.
Deployments across clinics, systems and employer populations.
Peer-review of patient-facing education for accuracy and tone.
Grand rounds, lectures and workshops co-hosted with partners.
Long-horizon collaborations across the sleep health ecosystem.
We're assembling a small founding advisory board across sleep medicine, behavioral sleep, chronobiology and health systems. Announcements will be made only after members formally join.
Codify the CBT-I, stimulus control and circadian evidence base underlying every recommendation.
Measure adherence, retention and self-reported outcomes across early cohorts.
Structured evaluations with partner sleep clinics on shared context and prepared appointments.
Co-authored publications with academic partners on longitudinal sleep behavior.
MyRemD partners with a small number of institutions per year — hospitals, sleep clinics, employers, research organizations, government and white-label partners. See how we work at scale.
No. MyRemD is a consumer-facing sleep health companion. It does not diagnose, treat or replace clinical judgment. Any medical decision-making remains with the treating clinician.
We work with a small circle of partners at a time. Engagements range from informal advisory to structured research protocols and enterprise pilots. Every partnership is scoped in writing.
Founding advisory participation is structured individually. We can discuss honoraria, equity or in-kind arrangements depending on scope and institutional policy.
Yes. Co-authored publications on longitudinal sleep behavior, adherence and CBT-I engagement are explicitly welcome.
Patients hold their data. Partners see aggregate, privacy-preserving signal unless a patient explicitly consents to share individual context with their clinician.
A short note is enough. We reply personally to every clinical and institutional inquiry.