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CRMO Care is now FlarePath. Same app, same data, new name.What changed
FlarePath

For clinicians

What your patients bring you.

FlarePath is a patient-reported data capture tool for kids and adults living with CNO/CRMO. Patients and families log between visits. You get one page you can read before you walk in the room.

FlarePathPatient-Reported Health Summary

SAMPLE

Patient SAMPLE-0142Age 11 · CNO/CRMO

Reporting period15 March–12 September 2026

Average reported pain
4.2/10
Check-ins recorded
129
Check-in rate
71%
Recorded fever episodes
1
Reported functional impact
High
Pain and functional-impact trendsPatient- or caregiver-reported entries during the selected period.
1050PainFunctionMarMayJulSepReported painFunctional impact
Pain and functional-impact trends
1Pain 3.1Function 7
2Pain 2.4Function 7.6
3Pain 5.8Function 4.2
4Pain 6.9Function 3.1
5Pain 6.2Function 3.6
6Pain 4.1Function 6
7Pain 3Function 7.2
8Pain 2.6Function 7.8
9Pain 5.4Function 4.8
10Pain 7.2Function 2.9
11Pain 6.4Function 3.4
12Pain 3.8Function 6.6
13Pain 2.9Function 7.4
14Pain 3.3Function 7.1
Sample data, not a real patient. Information is patient- or caregiver-reported and has not been verified against the medical record.

One page, before you walk in.

Families bring this to the appointment, or send it ahead through the portal. It is the same view they see in the app, so there is nothing to reconcile between what they remember and what was recorded.

  • Reporting period you choose. Since the last visit, or another window the family selects.
  • Completion rate shown on every report. You can see how much of the period is covered before you read anything into the trend.
How to refer a family

What is measured

What the current report shows.

DomainSourcePresentation
Reported painPatient or caregiver check-insAverage and trend over time
Functional impactPatient or caregiver check-insTrend over time
Fever episodesPatient or caregiver entriesRecorded episode count
Data coverageCompleted check-insCheck-in count and completion rate

Additional measures and report sections are being evaluated with families and clinicians. They are not included in the current report unless shown above.

Scope

What FlarePath does not do.

Stating this plainly is easier than having it discovered later. FlarePath is a data capture and reporting tool. Clinical judgement stays where it belongs.

  • It does not diagnose

    No diagnostic output, no scoring against diagnostic criteria, no differential.

  • It does not recommend treatment

    No dosing guidance, no escalation prompts, no suggestion to start or stop anything.

  • It does not alert or triage

    Nothing is routed to you between visits. It will not page you. Families are told: “FlarePath does not monitor entries. If you or your child needs urgent care, contact your care team or call 911.”

  • It does not replace the medical record

    FlarePath summarizes patient- or caregiver-reported information. Medication lists and other entries should still be reconciled against the medical record.

Referring a family

There is nothing for you to set up.

No account, no portal access, no data entry on your side. Patients and families sign up themselves and bring the report.

  1. Hand them the card

    A printed card with the link and a QR code. [ONLY PUBLISH IF CARDS WILL BE MAILED ON REQUEST]

  2. They sign up at home

    Free, with no insurance involved. Research sharing isn't live yet; when it is, it will be a separate opt-in.

  3. You get the report

    Printed, or sent ahead through your portal. A clinician view is planned but not yet available.

The open question

Does tracking this much actually help?

We have heard from pediatric rheumatologists that daily symptom capture may not serve every patient, and that for some people it risks making the illness the centre of daily life rather than something managed around it. That is a fair challenge and we do not think it is settled.

It is also a design question with a testable answer. A weekly instrument completed by most families may be worth more, clinically and scientifically, than a daily one completed by a third. We are measuring completion alongside everything else so the question can be answered with data rather than preference.

If you have a view on cadence, burden, or which measures actually change your management, we would like to hear it before we build more.

Tell us what you think

Research

Working with the data.

Families control whether they participate in research.

We are speaking with clinicians and research partners about how patient-reported, between-visit data could support future studies and registries. Research sharing is not currently active and would require separate family consent.

Start a research conversation