Education
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Overview
The Bleeding Disorders Council of California partners with the local bleeding disorders foundations, national organizations and rare disease partners to educate policymakers and the public about the needs of bleeding disorders and rare disease patients.
In particular, BDCC seeks to equip patients to understand and navigate potential barriers to access timely, affordable and quality health care.
View Our
Educational Events & Programs
to learn more about what we do, and how you can get involved.
WEBINAR SERIES
Informative online discussions that focus on understanding how your health care works and how to advocate for yourself.
LEARN MORECALIFORNIA RARE DISEASE ACCESS COALITION
A group that brings together advocates, providers, and stakeholders for improved care outcomes.
LEARN MOREHEALTH CARE ACCESS FORUMS
Quarterly member-exclusive meetings to discuss and address solutions to care and treatment issues.
LEARN MOREADVOCACY & ACCESS AMBASSADORS
A program that trains leaders to advocate on legislative and health policy initiatives.
LEARN MOREFUTURE LEADERS
A youth program that provides leadership training and develops advocacy skills for teens affected by bleeding disorders.
LEARN MOREFALL ADVOCACY DAYS
An event series that facilitate and encourage people to advocate in their own communities.
LEARN MORE
