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Accessibility Statement

Last updated: 2026-05-27

Forgotten Rare exists for families navigating rare disease and complex care, including many in the disability community. Accessibility is foundational, not optional.

What we work toward

  • Conformance with WCAG 2.1 AA as our target standard.
  • Semantic HTML, descriptive headings, and proper landmark regions for screen-reader users.
  • Keyboard-navigable interfaces, visible focus states, and a "skip to main content" link.
  • Color combinations chosen for sufficient contrast against our background palette.
  • Large tap targets sized for one-handed and assistive use.
  • Plain-language explanations of medical and insurance terms throughout the app.

Known limitations

Forgotten Rare is in active development. Some AI-generated content, third-party embeds, and evolving features may not yet meet our accessibility goals. We treat accessibility issues as bugs and prioritize them.

Tell us what's broken

If something is hard to use with a screen reader, keyboard, switch device, or any other assistive technology, please email accessibility@forgottenrare.com with the page and what you tried. We will respond and fix what we can.

Join the Forgotten Rare support list

Caregiver encouragement, new resources, financial help updates, and platform announcements. No spam — unsubscribe anytime.

Forgotten Rare provides educational, organizational, and emotional support only and does not provide medical, legal, insurance, financial, mental health, genetic counseling, or emergency advice. Always consult qualified professionals regarding your specific situation.

Not HIPAA compliant. Forgotten Rare is a personal support tool, not a medical records system. Please do not enter information you would not be comfortable storing outside of a HIPAA-protected environment. Avoid posting full identifiers (full name + date of birth + medical record numbers) and any data you are required to keep within a HIPAA-covered system.

© 2026 Forgotten Rare · In honor of Augyst

A portion of profits supports rare disease families.