Stay informed with the latest updates for the inheritable blood disorders community.

NBDF & Community
2025 Rare Disease Day
HANDI Highlights Looks Towards Rare Disease Day
Advocacy & Legislative
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Tune In! NBDF's Bill Robie Talks HB 1216 & Rx Costs
Advocacy & Legislative
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A Powerful BDAND Testimony in the Minot Daily News
Advocacy & Legislative
Capitol Hill Picture with flowers
Your Government Relations Update: January 2025
Advocacy & Legislative
A room where politicians meet with several empty seats
NBDF Advocates for Lower Out-of-Pocket Drug Costs in North Dakota
Medical
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FDA Approves New Non-Opioid Treatment for Pain
NBDF & Community
A group of diverse hands raised up
A Message from the Heart of NBDF
Advocacy & Legislative
Capitol Hill picture
Government Relations Update - December 2024
Medical
Diverse medical professionals
Clinical Practice and Hemophilia Gene Therapy the Focus of New…
Wildfire in the woods
Greater Los Angeles Wildfires: Community Support
Industry
Red blood cells bone marrow
Investigational Sub-Q Von Willebrand Disease Therapy Put on Fast Track
NBDF & Community
Boardroom
NBDF Welcomes New Board Members for 2025
NBDF & Community
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NBDF Joins Top Tier of Nonprofit Excellence
NBDF & Community
Dr. Valentino Becomes CEO
NBDF Celebrates the Appointment of Leonard Valentino, MD as President…
NBDF & Community
Diverse people on a globe
Global Experts Create Blueprint for Future VWD Research