Get diagnosed, get treated, get your life back!
ABDA Advocates for Policies Important to People Living with Behcet's Disease and with Rare Diseases
The American Behcet's Disease Association advocates for policies affecting the lives of patients and their families. Our efforts aim to affect change, actively work on proposals to protect and improve key policies at the local, state and federal levels and ultimately improve patient outcomes and quality of life. Addressing issues such as access to care, treatment innovations, research and healthcare policies, the voice of patients in policy and treatment development is of utmost importance. We encourage the community to reach out to elected officials through "call to action" initiatives.
"After many years of illness, my physician suspected a diagnosis of Behcet's Disease. Getting in touch with the American Behcet's Disease Association allowed me to connect with other patients and physicians with ample knowledge of BD and gave me hope. I'm no longer alone!" M. Kelly
WAYS TO HELP
Order Awareness Bracelets
Donate to the ABDA and receive free bracelets!
Become a Member
Becoming a member will provide recognition as a reliable contributor to the ABDA's advocacy and educational effort.
Patient Education Program & Walk for Behcet's Disease
As the outbreak of COVID-19 has been developing worldwide, ABDA has been closely tracking its impact on the global community. The Patient Education Program & Walk for Behcet's Disease have been postponed until next year. Our free educational webinars are planned for 2021. Please stay tuned.
Thank you for your constant support!
-The ABDA Board and Staff.