Education for Healthcare Professionals
We are committed to working with healthcare professionals to ensure patients receive the best treatment and care.
The rapid change of pace in research and treatments for amyloidosis makes it vital that healthcare professionals have access to up-to-date information on best practices. We provide unique resources and tailored information for doctors, nurses and other clinicians.
We collaborate with amyloidosis experts from around the world to design educational tools that provide clinicians with easy access to the most current information on scientific and clinical advances to help achieve earlier diagnosis and therapeutic intervention.
Physician Education & Tools
ARC Cardiac Amyloidosis Alert Card
This easy-to-use pocket card identifies “low voltage” EKGs in combination with ECHO images of increased ventricular mass, which are very...
Cardiac Amyloidosis: Stop Missing It! (CME/CE)
This symposium will provide a brief overview of cardiac amyloidosis, current guidelines and emerging options for treatment, and how to...
Medscape CME & Education for Physicians
Medscape is the leading online global destination for physicians and healthcare professionals worldwide with the latest medical news and expert...
Clinical Resources APP
Learn how this valuable tool is giving healthcare professionals easy access to critical and current medical information and improving early and accurate diagnosis of amyloidosis.
Amyloidosis Support Groups has been hosting these meetings for our hereditary and wild type patients since 2009. The group has grown from 85 at the first meeting to over 400 in 2017. With more treatments and clinical trials, these meetings have become vitally important and life altering.
The 61st ASH Annual Meeting & Exposition is the world's most comprehensive hematology event of the year. The meeting will provide an invaluable educational experience, and the opportunity to review thousands of scientific abstracts highlighting updates in a variety of hematology topics. Network with top minds in the field and a global community of more than 25,000 hematology professionals from every sub-specialty.
Rare Disease Week attracts hundreds of patient advocates from around the country to Washington, DC for a week of events dedicated to empowering patients, families, and friends to become legislative advocates. Advocates will have an opportunity to meet with Members of Congress and learn best practices for successful advocacy. No advocacy experience required. The travel stipend application for Rare Disease Week is open. Deadline to apply for a travel stipend is December 2, 2019. You can apply here. Registration for Rare Disease Week on Capitol Hill opens on January 3, 2020.