With more than 30 million rare disease patients in the United States, the rare disease community is diverse in race, ethnicity, religion, and socio-economic circumstances. Because the rare disease community encompasses individuals from all walks of life, the RARE Foundation understands the need for linguistically diverse and inclusive material. The Foundation is committed to providing resources in multiple languages and ensuring that every advocate, regardless of primary language spoken, can advocate and have their voice heard.
Transcription and Translation Services Resources and References
- DC Municipal Government Approved and Vetted Vendors (Interpretation and Translation)
- Census Search for Race and Ethnicity per state and City
