Vote for your favorite 2024 World Hemophilia Canvas!
April 11, 2024
To celebrate Bleeding Disorders Awareness Month and World Hemophilia Day, members of the WPBDF community were sent 4 x 4
April 11, 2024
To celebrate Bleeding Disorders Awareness Month and World Hemophilia Day, members of the WPBDF community were sent 4 x 4

March 29, 2024
Constance is diagnosed with von Willebrand Disease (VWD), and like many other women in the bleeding disorders community, did not

March 27, 2024
At two years old, Cassie accidentally received her diagnosis of Type 1 von Willebrand Disease, severe, when she was scheduled

March 22, 2024
Educational Grants are Available for NBDF’s 2024 Bleeding Disorders Conference The Western Pennsylvania Bleeding Disorders Foundation (WPBDF) is pleased to

March 21, 2024
Before Jessamyn received her bleeding disorder diagnosis, she had terrible, long, and miserable periods. Her family had a long history

March 12, 2024
Who is eligible for the WPBDF Scholarship? Any person or immediate family member of a person with hemophilia, von Willebrand Disease,

March 7, 2024
Marisa has mild hemophilia A, but she didn’t receive her diagnosis until she was 31 years old. Growing up as

February 5, 2024
Program and Events Coordinator Summer 2024 Internship Summary Responsible for assisting in planning and managing WPBDF’s programs and fundraising initiatives; including the

January 29, 2024
Did you know you can request a review of denied health insurance claims online? If your health plan has denied a
November 29, 2023
There are many meaningful ways for you to invest your time, creativity, and talents to help WPBDF operate efficiently and

October 27, 2023
Program and Events Coordinator Spring 2024 Internship Western Pennsylvania Bleeding Disorders Foundation Summary Responsible for assisting in planning and managing WPBDF’s programs and fundraising

August 31, 2023
Team 4 Rare Kids is made up of the team captains, Christy and Jason, and their children, Seth, Spencer, Xavier,
August 24, 2023
By Identifying as a ‘Leading Patient Advocate,’ Payer Matrix Puts Patients in Jeopardy New York, NY (August 24, 2023) – 34 patient

August 10, 2023
Hemophilia Federation of America is excited to once again offer their Mild Matters Summit, created for adults with mild bleeding

August 7, 2023
On Saturday, August 6, 2023, Megan W. hosted a fundraiser for her senior project to help raise funds for the
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