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Von Willebrand Disease (VWD) - Online Support Group

Welcome aboard, Kya from North Dakota

@Kya

Hello and welcome to Living With VWD! Let our wonderful community join you in collectively hoping that your daughter’s situation will improve greatly now that you have found her a new treatment center. Don’t hesitate to give us an update on her or ask any questions about other’s experiences - I know many other members around here have also joined on behalf of their children. You can even look through some of these old topics yourself, if you’d like, or search for something in particular by using the Search Icon (top right of the red bar).

Best wishes for your family - and let me know if you ever have any questions!