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Topic: hematologic diseases (he)
Title: All About Von Willebrand Disease...For People With Von Willebrand Disease And Their Families. 2nd ed.
Author: Page, D.
Source: Montreal, QC: Canadian Hemophilia Society. 2007. 87 p.
Availability: Available from Canadian Hemophilia Society. 625 President Kennedy, Suite 505, Montreal, QC H3A 1K2. Phone: 1-800-668-2686. Email: chs@hemophilia.ca. Website: www .hemophilia.ca. Price: Available free of charge on website.
Abstract: This monograph from the Canadian Hemophilia Society provides comprehensive information about von Willebrand disease (VWD), a disease characterized by problems in the von Willebrand factor (VWF). The VWF is a protein in the blood that is necessary for proper blood coagulation. When there is not enough VWF in the blood, or when it does not work the way it should, the blood takes longer to clot. This booklet reviews the different types of VWD, the role of heredity, the symptoms, diagnostic tests that can confirm the condition, treatment options, and strategies for healthy living with VWD. The lifestyle factors discussed include the safety of blood products, coping with nose bleeds, conception, pregnancy and childbirth, medications to avoid, exercise, fitness and sports, child care, schooling, employment, insurance, traveling, and medical identification. The booklet concludes with the contact information for the Canadian Hemophilia Society, a list of hemophilia or bleeding disorders treatment centers in Canada, a glossary of terms, a subject index, and a bibliography. The booklet includes black-and-white illustrations. 6 references.

Format: Monograph/Book
Language: English.
Major Keywords: Hematologic Diseases. Von Willebrand Disease. Antihemophilic Factor. Symptoms. Diagnosis. Therapy. Patient Care Management.
Minor Keywords: Genetics. Blood Diseases and Disorders. Diagnostic Tests. Lifestyle. Activities of Daily Living. Coagulation. Risk Factors. Quality of Life. Patient Education.
Publication Number: HEBK10176.
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