Where can one find more information about Von Willebrand disease?
* The Von Willebrand Society (VWS): The VWS is a non-profit organization dedicated to increasing awareness and understanding of Von Willebrand disease. Their website has information about the disease's history, research efforts, upcoming events, and links to support groups.
* The National Hemophilia Foundation (NHF): The NHF is another non-profit organization that provides support and information to individuals with bleeding disorders, including Von Willebrand disease. Their website has information about the disease, treatment options, and financial assistance programs.
* The American Society of Hematology (ASH): The ASH is a professional society for hematologists, which are doctors who specialize in the study and treatment of blood disorders. Their website has information about Von Willebrand disease, upcoming conferences and educational opportunities.
* MedlinePlus: This is a free online library that provides information about various medical conditions, including Von Willebrand disease. Their website has information about the disease's symptoms, diagnosis, and treatment options.