Help Center
Quick-reference cards. For in-depth docs, see Documentation.
Looking for the full documentation?
Deep guides on every module, every workflow, the safety model, and the technical layer.
Open Documentation →Guides by role
Patient guide
Organize your diagnosis, track symptoms and treatments, store records, and prepare for visits.
Read →Caregiver guide
Help someone manage their cancer journey once they've granted you access.
Read →Clinician guide
Read a patient's organized record and their one-page summary — with their consent.
Read →Researcher guide
Explore the public data bank and research-only tumor-state tooling. Never identified patient data.
Read →Admin guide
Operate the platform: audit trail, data bank seeding/ingestion, and research exports.
Read →Quick start
What Teloma is
Teloma is a cancer journey observability platform. It helps you organize your records, track how you feel and respond over time, and produce a clean summary for appointments — for any cancer type.
Teloma is NOT medical advice. It does not diagnose, recommend or rank treatments, provide dosing, or replace your care team.
Signing in
Go to /sign-in. In this demo you can sign in with an email and a role (Patient, Caregiver, Clinician, Researcher, Admin) — no password.
Patients land on the Dashboard. Clinicians and caregivers see the people who have granted them access.
The big picture
Symptoms are your logs, labs/vitals are metrics, diagnosis/biopsy/treatment/imaging are events, pathology/genomics/biomarkers are system state, and response/progression/recurrence are outcomes.
Everything you enter flows into one Timeline and can be rolled up into a one-page Clinician Summary.
Frequently asked questions
Is Teloma medical advice?
No. Teloma organizes and tracks your information and produces summaries. It does not diagnose, recommend or rank treatments, or provide dosing, and it does not replace your care team.
Does it support my cancer type?
Yes — Teloma supports all cancer types. The diagnosis and biomarker fields are generic, so any cancer and any marker can be recorded.
Who can see my data?
Only you, plus any clinician or caregiver you grant access to (revocable anytime). Researchers never see identified data. Every access is audited.
What does research consent mean?
If you opt in, a de-identified copy of your records may be included in research datasets. It's optional, separate from clinician access, and you can withdraw at any time.
Can I export my summary?
Yes — generate a clinician summary and download it as a PDF to bring to appointments.
Architecture, data model, runbook, and source docs also live in the docs/ folder of the repository.