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
July 26, 2023
Eager to get involved with WPBDF, Ashley and her family joined the Unite for Bleeding Disorders Walk in 2022 with
June 5, 2023
Enjoy dinner, visit sponsor booths, and learn about the WPBDF’s services at the Annual Meeting! Everyone who attends is invited to
April 20, 2023
Summary Responsible for assisting in managing WPBDF’s fundraising initiatives; including the development, planning and execution of special events. WPBDF offers a
April 19, 2023
We have an exciting opportunity to advance the Safe Step Act and the HELP Copays Act. The Senate HELP Committee
April 11, 2023
Hemophilia, von Willebrands Disease, or any other bleeding disorder? No problem! Fly into this fine-feathered hike and game for fun physical
April 3, 2023
To celebrate Bleeding Disorders Awareness Month and World Hemophilia Day, members of the WPBDF community were sent 4 x 4
March 22, 2023
Who is eligible for the WPBDF Scholarship? Any person or immediate family member of a person with hemophilia, von Willebrand Disease,
February 3, 2023
Do you or a family member currently have health coverage through Medicaid or the Children’s Health Insurance Program (CHIP)? If
January 11, 2023
We are looking for individuals who are interested in supporting the advocacy efforts of the Pennsylvania Bleeding Disorders Foundations throughout
January 3, 2023
NHF’s Washington Days is an opportunity for people affected by inherited blood disorders to advocate for issues important to them.
Giving back is as simple as one dollar, one day, one moment. You can change the tomorrow of someone in need. Join Us.