9/14/2020 Update: If you were unable to join us for our live sessions or are interested in re-watching sessions from the conference, we've made the pre-recorded Basics webinars and portions of select live sessions available. Click here and use your registration login info to access the recorded sessions.

8/30/20 Update: Those who have registered have received directions via email on how to access the conference sessions. If you have not yet registered for the conference, please register using the button above, and you will receive an email shortly after with instructions on how to access the sessions.

Welcome to the Rare Bleeding Disorders Virtual Conference!

The Rare Bleeding Disorders Virtual Conference is a unique experience to connect, learn and grow with individuals and families affected by rare bleeding disorders from around the world. This year, in order to keep our community safe and help prevent the spread of COVID-19 we have made the decision to host the 2020 Rare Bleeding Disorders Conference virtually.

The Rare Bleeding Disorders Conference will be held from August 30 – September 4, 2020.

We’re excited to bring this virtual experience to you and your family. We see this as an amazing opportunity to expand our programming to provide engaging education and perspectives for families affected by factor V, VII, X, XI, XIII, Glanzmann's Thrombasthenia, and rare platelet disorders! Our time together will include educational sessions on various rare bleeding disorders, intimate provider – patient Q&A sessions, networking opportunities and social experiences for all ages. This year, we are also bringing the first ever virtual Rare Bleeding Disorders Conference Youth Camp!

Can’t wait to see you there!

Virtual Youth Camp

Join us for the National Hemophilia Foundation’s first ever virtual Rare Bleeding Disorders Conference youth camp: Camp Unite!

Amazing Sessions

Expanded programming to provide engaging education and perspectives for families affected by factor V, VII, X, XI, XIII, Glanzmann's Thrombasthenia, and rare platelet disorders!

 
 

 

Our Sponsors


At NHF we cannot do the work we do without the support of our amazing sponsors.