HelpFindMyCure

Dignity, permission and control

Patient Bill of Rights

These rights describe how the product is designed to behave. Implementation continues to deepen; we do not invent certifications or outcomes.

1. Privacy

Your case is private by default.

2. Respect

Your health story is treated as lived experience, not a dataset.

3. Transparency

You can see who has access and why.

4. Control

You decide who may participate and what they may see.

5. Informed consent

Important authorizations generate readable receipts.

6. Access visibility

Access history is presented in understandable language.

7. Revocation

You can revoke access where operationally possible.

8. Correction

You can review, confirm, correct or dispute extracted information where supported.

9. Portability

You should be able to retrieve your information where supported.

10. Human review

Medical action remains under qualified clinical authority.

11. AI transparency

Material AI outputs show provenance and are not presented as physician-authored.

12. Source transparency

Research claims should connect to evidence and original sources.

13. Security

Security claims describe actual controls—not slogans.

14. Non-discrimination

Access and participation must not be designed to discriminate.

15. Accessibility

Core flows target WCAG 2.2 AA usability.

16. Complaint mechanisms

You can raise privacy, access, AI and safety concerns.

17. Commercial transparency

Funding and commercial relationships will be disclosed as they exist—never invented.

18. Clear deletion practices

Deletion controls must explain what is removed and what may be retained.

19. Accurate representation of expertise

Credentials and roles must not be exaggerated.

20. No fabricated outcomes

We do not invent patient stories, cure claims or unverifiable results.