About Us
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About Us
Rare Disease Advocates (RDA) is a nonprofit organization founded by a diverse coalition of healthcare professionals dedicated to improving the diagnosis, treatment, and overall experience of individuals facing rare and complex diseases. We empower both healthcare providers and patients through education, advocacy, support, and innovation—creating lasting change in healthcare delivery and equity.
While our roots are in rare diseases, our mission has grown to address gaps in care across all underserved or misunderstood disease states. By equipping providers with tools for early recognition and evidence-based management—and by offering patients the support and resources they deserve—we bridge the gap between diagnosis and compassionate, effective care.
Our Mission:
At RDA, our mission is to:
Educate Providers: Deliver expert-led training and educational programs and clinical tools to enhance provider understanding of diagnosis and optimal treatment.
Provide Financial Support: Offer inclusive, financial support for those navigating complex healthcare journeys.
Raise Awareness: Increase public and clinical understanding of underrecognized diseases, while spotlighting the challenges faced by patients and families.
Advocate for Change: Champion health policy, research funding, and systemic improvements that benefit both rare disease communities and other overlooked populations.
Our Values:
Collaboration: We partner across disciplines, institutions, and communities to amplify impact.
Empowerment: We equip patients and providers alike with knowledge and agency.
Compassion: We approach every individual and family with empathy and dignity.
Innovation: We embrace creative, data-informed solutions to overcome complex challenges in care delivery.
Our Commitment:
RDA is committed to driving real-world impact through:
Listening: Centering the voices of patients, caregivers, and clinicians in everything we do.
Educating: Providing reliable, up-to-date, and practical information for both medical professionals and the communities they serve.
Advocating: Promoting equitable access to care, research, and resources through grassroots and legislative initiatives.
Supporting: Delivering peer connection, guidance, and holistic resources that meet the physical, emotional, and social needs of those affected.
Donations made to Rare Disease Advocates are tax-deductible and directly support our mission-driven programs.
Your Financial Contribution Can Help Us Fund Critical Programs & Initiatives
As a Nonprofit organization, we are deeply committed to raising awareness, providing patient support, and advocating for better resources and research for individuals living with rare diseases.
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For general questions about our organization, our mission, or how you can get involved, please email us. We endeavor to respond to all inquiries