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Home
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    • Our Story
      • Mission & History
      • What We Do
      • What Do We Value?
      • Health Access
      • NBDF Reports
      • Financial Statements
      • Media Newsroom
      • Educate to Elevate
      • The National Hemophilia Foundation Has a New Name
      • The Red Thread: 75th Anniversary Celebration
    • Our Team
      • Staff
      • Board of Directors
      • MASAC
      • Meet the NYLI
      • Nursing Working Group
      • Physical Therapy Working Group
      • Social Work Working Group
      • LEE Research Advisory Council
    • Our Partners
      • Partners In Progress
      • The ACT Initiative
      • Red Tie Society
      • CDC Coop Agreement
      • Pathway to Cures
    • Careers
      • What Do We Value?
      • Career Opportunities
      • Volunteer Opportunities
  • Bleeding Disorders A-Z
    • Overview
      • Fast Facts
      • What is a Bleeding Disorder?
      • History
      • Types of Bleeds
      • Inhibitors
      • Women and Bleeding Disorders
    • Types
      • Hemophilia A
      • Hemophilia B
      • Von Willebrand Disease
      • Other Factor Deficiencies
      • Inherited Platelet Disorders
    • Treatment
      • Comprehensive Medical Care
      • MASAC For You
      • Treatment Guidelines (MASAC)
      • Current Treatments
      • Innovative Therapies
      • Clinical Trials
      • Shared Decision-Making
      • Hemophilia Treatment Centers
    • Healthcare Coverage
      • Choosing an Insurance Plan
      • Private Insurance
      • Public Insurance
      • Health Insurance Toolkit
  • Educational Programs
    • Education
      • Bleeding Disorders Conference
      • Inhibitor Education
      • Steps for Living
      • Online Education
      • Rare Bleeding Disorders
      • Von Willebrand Disease
      • Mental Health
      • Gene and Innovative Therapies
      • Women
      • Educational Programming
      • Clotting Cascade
    • Training
      • Youth Leadership (NYLI)
    • Outreach
      • THRIVE
      • THRIVE - en español
      • Undiagnosed
      • Guías Culturales
  • Advocacy
    • Federal Priorities
      • Access to Care
      • Federal Programs
      • Medicare
      • Medicaid
      • Blood & Blood Product Safety
      • Make All Copays Count
    • State Priorities
      • Utilization Management
      • Patient Out-of-Pocket Expenses
      • Medicaid
    • How You Can Take Action
      • Voices for Policy Change!
      • Washington Days
      • Advocacy Do’s and Don’ts
      • 6 Steps for Grassroots Advocacy
      • Tell Your Story
    • Managed Care & Payers
      • Collaborating on Coverage
      • Quality of Care Guidelines
      • CME/CE Webcast Series
      • Educational Web Portal
      • Quality Improvement & Cost Management
  • Research
    • Research Projects
      • Foundation Research
      • Funded by Foundation
      • Presented at Our Conference
      • Research Journal Club
      • Research Roundtable
      • Clinical Trial Essentials
      • coreHem Mental Health Tool
    • Fund Your Research
      • Judith Graham Pool Postdoctoral Research Fellowship
      • NBDF-Sanofi Career Development Award
      • Nursing Excellence Fellowship
      • Physical Therapy Excellence Fellowship
      • Social Work Excellence Fellowship
    • Community Voices in Research
      • What is CVR?
      • How & Why Should I Participate?
      • Impact on Research
      • Frequently Asked Questions
      • Login to CVR
    • Bleeding Disorders Research Collaborative
      • What is the Bleeding Disorders Research Collaborative?
      • The BDRC Structure and Research Priorities
      • Lived Experience Experts (LEEs) Leading the Way
      • How to Get Involved
      • Our Journey Together
      • BDRC Resources
  • Healthcare Professionals
    • Guidelines on Care
      • Comprehensive Care
      • MASAC Documents
      • MASAC Minutes
      • Products Licensed (US)
      • Emergency Management
      • Snapshots of VWD Guidelines
    • Education & Resources
      • NBDF-Takeda Clinical Fellowship Program
      • NBDF’s Collaborative Learning Exchange
      • Online Education for Providers
      • Live & Online Learning (Partners)
      • Rare Coagulation Disorders Resource Room
      • Peer-reviewed Journals
      • NBDF Publications
      • Other Associations
    • Allied Healthcare
      • Nursing
      • Physical Therapy
      • Social Work
      • Other Interdisciplinary Healthcare Providers
  • Community Resources
    • Request Information
      • Contact Us
      • The Neil Frick Resource Center
      • Read Our Publications
      • Subscribe for Email Updates
      • Get HemAware Magazine
      • Newsletter Archive
      • Wednesday Webinar Series
    • Resources Near You
      • Chapters
      • Hemophilia Treatment Centers
      • Clinical Trials
      • Bleeding Disorders Camps
      • Community Voices in Research
    • Financial Assistance
      • Scholarships
      • Patient Assistance Programs
  • Make a Difference
    • Donate
      • Donate Now
      • Donor Advised Funds
      • Donate Securities or Cryptocurrency
      • Give Monthly
      • Planned Giving
    • Join Us
      • Become a Corporate Partner
      • Bleeding Disorders Awareness Month
      • Find a Walk
      • Participate in Research/CVR
      • Why Give?
    • More than a Donation
      • Create Your Own Fundraiser
      • Fundraise on Social Media
      • Run in a Marathon
      • Matching Gifts
  • Give
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Inequities in Thrombosis and Hemostasis Lab Testing the Focus of Illustrated Review
A new illustrated review published in the journal Research and Practice in Thrombosis and Haemostasis makes the case that many established reference intervals (RIs) used to interpret the results of laboratory tests are biased and highly problematic…
Shaping the Future: Search Begins for New NHF CEO
Dear Valued Partners, Recently Dr. Len Valentino, President and CEO of the National Hemophilia Foundation, announced his retirement at the end of 2023 and the search for a new leader has begun. Under Dr. Valentino’s leadership, NHF has taken…
Lived Experience Experts (LEEs) Leading the Way
 The BDRC (formerly the NRB) is organized to enable people affected by inherited bleeding disorders and their loved ones – recognized as lived experience experts (LEEs) – to actively participate and influence the direction of transformational…
First Hemophilia B Patient Dosed with Gene Therapy Product
CSL Behring has announced that the first patient has been dosed with HEMGENIX®, the only hemophilia B gene therapy product currently approved in the U.S. Approved by the U.S. Food and Drug Administration in November 2022, HEMGENIX is indicated…
Patient-Clinician Partnerships the Theme of ASCO Presidential Address
Earlier this month The American Society of Clinical Oncology (ASCO) held their annual meeting in Chicago, IL. The opening session presentation was delivered by ASCO President Eric P. Winer, MD, FASCO, a dedicated clinical oncologist for more than 30…
The National Hemophilia Foundation Has a New Name
  NBDF History In 1948, the foundation got its start as simply “The Hemophilia Foundation” – then in 1956, the foundation formally incorporated into what is known today as – the National Hemophilia Foundation. Even then, it was…
The Clotting Cascade
#block-recentonlineeducation { display:none; } Clotting Cascade 3D VideoCome along on a 3D adventure in this video about how blood clots when there is a bleed or injury. The 3D animation in this video shows each of the proteins (called clotting…
Hemophilia A Gene Therapy Product Receives U.S. FDA Approval
The U.S. Food and Drug Administration (FDA) has approved BioMarin’s ROCTAVIAN™ (valoctocogene roxaparvovec-rvox) gene therapy product for the treatment of adults with severe hemophilia A without antibodies to adeno-associated virus serotype 5 (AAV5…
Helen Lamping
New Trial Data Shows ALTUVIIIO™ Prophylaxis Effective in Children
Sanofi recently shared positive data from the Phase 3 XTEND-Kids study, which is currently evaluating once weekly prophylaxis with ALTUVIIIO™ in previously treated patients younger than 12 years of age with severe hemophilia A.ALTUVIIIO is Sanofi’s…

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