The more you know, the better
partner you become in your
own care.

Where can I go for more information?

One of the most important things you can do after a von Willebrand disease (VWD) diagnosis is to educate yourself on how it impacts your life. Included here are links to basic facts, resources you should be aware of, and an opportunity to join our VWD mailing list. Bookmark this page for quick access to all the resources you may need moving forward with VWD.

Learn about VWD resources
Learn about VWD resources
Learn VWD topics to discuss with a HCP
Learn VWD topics to discuss with a HCP

Discussion Guides

What questions should I ask my HCP about VWD?

Not sure what to discuss about VWD when you talk to your healthcare provider? Download some of our HCP discussion guides to help start the conversation.

They focus on:

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Your Journey

Take the poll and see how other members of the VWD community answered.

What type of bleeds do you most commonly have?

of Beyond the Bleed visitors had the same answer you did. Read more about diagnosis.

What are my options for managing VWD?

Learn how comprehensive care at an HTC plans personalized care

Find out about it

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