Your experience. Our future.

A patient, caregiver, and clinician registry for real-world cannabis healthcare experience.

Share symptoms, goals, cannabis use or non-use, outcomes, side effects, and access barriers in a plain-language format designed to support research, learning, and better understanding across real care experiences.

Before you begin

This survey works for patients, caregivers, and clinicians through one shared entry point.

The wording adjusts after the first questions so each person sees a flow that fits their role.

Who should use this

Anyone sharing their own experience, answering for someone else, or contributing clinician observations.

What is optional

Many questions can be skipped. Future-contact information stays separate from the main survey data.

Start the registry survey

Patients, caregivers, and clinicians all belong in the recordPlain-language flow with role-aware wordingOptional future contact only if you choose it

Plain-language survey

Designed to be completed one screen at a time without clinical jargon.

One shared entry point

Patients, caregivers, and clinicians all start from the same survey and branch from there.

Research, not emergency care

Built for research and learning, not diagnosis or urgent clinical support.

Choose Your Path

One survey, three respondent paths

You do not need a separate link for each audience. Start once, choose the role that fits, and the survey adjusts the wording and route from there.

Patients and participants

Share your own experience with symptoms, cannabis use or non-use, outcomes, side effects, cost, and access barriers.

Parents and caregivers

Answer for a child, dependent, or another person in your care. The survey adjusts its wording once you choose that route.

Clinicians

Contribute either one patient-focused response or broader practice-level observations without patient identifiers.

Ready To Start

Start the survey when you are ready

You do not need special preparation. Choose the role that fits, answer in plain language, and share only what you are comfortable entering.

Continue to survey

If you want more background first, the public document library stays available below.

Privacy And Trust

Survey answers and optional follow-up are handled separately

The main survey response can stand on its own. If someone wants updates or future follow-up, the contact details needed for that are handled separately rather than mixed into the core response record.

Main response record

Symptoms, goals, use patterns, outcomes, safety, and access barriers.

Optional future contact

Contact details only if someone chooses updates or future follow-up.

Read privacy and consent

Supporting Materials

Keep the background material available, but secondary

These pages are optional reading for people who want more context before or after they respond. They are not required to complete the survey.

About this registry

See what the registry is for, who it serves, and why these responses matter.

Privacy and consent

Read the consent notes and privacy framing before sharing a response.

After you submit

Understand what confirmation means and what the participant summary does and does not represent.

Staff And Internal Use

Registry staff, reviewers, and governance users can access the protected workspace separately. This entry is here for internal operations, not for survey participants.