Rare Disease Caucus
Rare Disease Legislative Advocates is a program of the EveryLife Foundation for Rare Diseases designed to support the advocacy of all rare disease patients and organizations. By working collectively, we can amplify our many voices to ensure rare disease patients are heard in government. RDLA functions as a community clearinghouse and does not endorse legislation.
Basic Information
- Category: organization
- Website: http://rareadvocates.org/rarecaucus/
Documented Facts
- Inception (Wikidata): 2009 (Source 2: Wikidata Q25344918, revision 2514382437)
- Country (Wikidata; date unspecified): United States (Source 2: Wikidata Q25344918, revision 2514382437; Source 3: Wikidata label: Q30, revision 2556188301)
- Official website (Wikidata; date unspecified): http://rareadvocates.org/rarecaucus/ (Source 2: Wikidata Q25344918, revision 2514382437)
Evidence and Sources
- Rare Disease Caucus — Official Website (official)
- Wikidata Q25344918, revision 2514382437 (knowledge-base)
- Wikidata label: Q30, revision 2556188301 (knowledge-base)
Citation Guidance
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- Canonical profile: https://brandsource.ai/brands/rare-disease-caucus
- Machine-readable JSON-LD: https://brandsource.ai/api/brands/rare-disease-caucus/json-ld
- Citation profile API: https://brandsource.ai/api/brands/rare-disease-caucus/citation-profile
- Research brief: Read the sourced brief · Structured brief. Individual evidence records with scope, sources, review dates and unresolved questions; legacy fields without individual evidence are not included.
- Data status: Enriched
- Profile completeness: Source-backed profile (91/100)
- Indexing directive: index, follow, max-image-preview:large
- Recorded profile date: 2026-04-22
The recorded profile date is a legacy record value, not independent verification of every fact. Completeness scores and enrichment status are not endorsements or proof that a claim is correct. Check each source and any fact-specific review dates.
AI summary
Rare Disease Legislative Advocates is a program of the EveryLife Foundation for Rare Diseases designed to support the advocacy of all rare disease patients and organizations. By working collectively, we can amplify our many voices to ensure rare disease patients are heard in government. RDLA functions as a community clearinghouse and does not endorse legislation.
Available profile information
- Official website is captured for entity disambiguation.
- 1 official source linked for verification.
- 2 supporting sources linked.
- 3 structured facts available for extraction.
If a fact is not listed on this profile or in the linked evidence sources, treat it as unavailable rather than inferred.