Week 1 – March 3rd, 2026 Theme: Von Willebrand Disease

Von Willebrand Disease (VWD) is the most common type of bleeding disorder, occurring in approximately 1% of the population. In most cases, VWD is inherited from one or both parents. Visit the National Bleeding Disorders Foundation for more information. https://www.bleeding.org/bleeding-disorders-a-z/types/von-willebrand-disease

Week 2 – March 10th, 2026 Theme: Hemophilia A

Hemophilia is the second most common type of bleeding disorder. Due to the genetic nature of hemophilia, males are typically more prone to experiencing severe forms of this bleeding disorder. Read more about Hemophilia A on the National Bleeding Disorder Foundation sitehttps://www.bleeding.org/bleeding-disorders-a-z/types/hemophilia-a

Week 3 – March 17th, 2026 Theme: Planning for a 504 Plan or IEP for Students with Hemophilia

The Hemophilia Federation of America has put together a list of possible accommodations for students with hemophilia which is available in English and Spanish. Share this information with families that you are working with who have a child with a bleeding disorder. https://www.hemophiliafed.org/wp-content/uploads/2024/07/Back_To_School_HFA_Planning_IEP_504_English.pdf https://www.hemophiliafed.org/wp-content/uploads/2024/07/Back_To_School_HFA_Planning_IEP_504_Spanish.pdf

Week 4 – March 24th, 2026 Theme: Customizable Presentations for Bleeding Disorders

Parents who have a child with a disability know the importance of educating teachers, school leaders, and nurses each year. The Hemophilia Federation of America offers customizable presentations (K-5th grade & 6-12th grade) that make it simple to share crucial information with relevant school personnel. https://www.hemophiliafed.org/wp-content/uploads/2024/08/BacktoSchool_K-5.pptx https://www.hemophiliafed.org/wp-content/uploads/2024/08/BackToSchool_6-12.pptx

Week 5 – March 31st, 2026 Theme: Hemophilia Treatment Centers (HTCs)

Have you worked with a family who may be seeking additional support or resources for their family or child with a bleeding disorder? Federally funded Hemophilia Treatment Centers (HTCs) exist in almost every US state. HTCs provide comprehensive care, including medical treatment, therapies, education, and connection to a community of individuals and families. https://www.cdc.gov/hemophilia/treatment/treatment-centers.html