Treatment trials
Keep medications, dates, dosages, and reasons for stopping together.
MIGRAINE TREATMENT HISTORY · PRIVATE BETA
Your migraine treatment.
One clear history.
Record clinician-directed medication trials, what happened, and what to bring to your next appointment. Fast to update. Yours to review and share.
WHAT EASE DOES
Everything you need.
Nothing you don't.
Quick outcome logging
Record benefit, side effects, and migraine days in a few taps, even on difficult days.
Privacy first
You decide what to record and when to share it. We do not sell your personal data.
Treatment timeline
See past and current medication trials in one chronological, patient-owned record.
Appointment-ready reports
Turn your history into a concise summary to review with your clinician.
Low-burden check-ins
Short prompts keep your history current without asking for a long daily diary.
OUR APPROACH
Built for the reality of migraine treatment.
Appointments are short and treatment histories get fragmented. Ease keeps the details together without adding another demanding routine.
1 TREATMENT HISTORY
3 CORE OUTCOMES
YOU CONTROL SHARING
MON 28
TUE 29
WED 30
THU 31
FRI 1
SAT 2
SUN 3
YOUR RECENT HISTORY
ROADMAP
From a clear treatment history
to better-informed appointments.
Now Phase 1
Treatment History
- Clinician-directed medication trial records
- Quick benefit and side-effect logging
- Migraine-day and severity history
- Patient-owned chronological timeline
- Appointment-ready report export
In development Phase 2
Workflow Validation
- Beta-user interviews and usability testing
- Clinician review of the report format
- Low-burden outcome measures
- Consent and data-governance workflows
- Pilot operations and support workflows
Planned Phase 3
Shadow Research
- Prospective observational cohort
- Pre-specified evaluation protocol
- No user-facing predictions or treatment advice
- Calibration and subgroup performance checks
- Independent clinical and statistical review
Target Phase 4
Regulated Product, If Validated
- Intended-purpose and classification assessment
- Quality and risk management systems
- Clinical performance and utility evidence
- Human factors and cybersecurity validation
- Regulatory submission only after evidence gates