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Home
  • Who We Are
    • Our Story
      • Mission & History
      • What We Do
      • What Do We Value?
      • Health Equity
      • Accomplishments
      • Financial Statements
      • Media Newsroom
      • 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
    • Our Partners
      • Partners In Progress
      • The ACT Initiative
      • Red Tie Society
      • CDC Coop Agreement
      • Pathway to Cures
    • Careers
      • What Do We Value?
      • Job Openings
      • 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
      • Future Therapies
      • Clinical Trials
    • Healthcare Coverage
      • Choosing an Insurance Plan
      • Private Insurance
      • Public Insurance
      • Health Insurance Toolkit
  • Educational Programs
    • Education
      • Bleeding Disorders Conference
      • Inhibitor Education
      • Online Education
      • Rare Bleeding Disorders
      • Von Willebrand Disease
      • Mental Health
      • Gene and Innovative Therapies
      • Women
      • Educational Programming
      • Own Your Path
      • Clotting Cascade
    • Training
      • Youth Leadership (NYLI)
    • Outreach
      • 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
      • Register to Vote
      • 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
      • Clinical Trial Essentials
    • Fund Your Research
      • Judith Graham Pool Postdoctoral Research Fellowship
      • Career Development Award
      • Bridge Award
      • Innovative Investigator Research Award
      • Jeanne Marie Lusher Diversity Fellowship
      • 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
      • What We’ve Learned So Far
    • National Research Blueprint
      • What is the National Research Blueprint?
      • Involvement from Across the Community
      • Lived experience experts (LEEs) leading the way
      • Building the Blueprint
      • Research Priorities
  • Healthcare Professionals
    • Guidelines on Care
      • Comprehensive Care
      • MASAC Documents
      • Products Licensed (US)
      • Emergency Management
      • Snapshots of VWD Guidelines
    • Education & Resources
      • NHF-Takeda Clinical Fellowship Program
      • NBDF’s Collaborative Learning Exchange
      • Online Education for Providers
      • Live & Online Learning (Partners)
      • Rare Coagulation Resource Room
      • Peer-reviewed Journals
      • NBDF Publications
      • Other Associations
    • Allied Healthcare
      • Nursing
      • Physical Therapy
      • Social Work
  • Community Resources
    • Request Information
      • Contact Us
      • HANDI - NBDF's Information 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
    • Financial Assistance
      • Scholarships
      • Patient Assistance Programs
  • Contact Us
  • Subscribe
  • News
  • Events
  • Give
    • Give Now
      • Make a Donation
      • Give Monthly
      • Honor a Loved One
      • Support Research
      • Why Give?
      • Kevin Child Scholarship Donation Form
      • Physician Partners
    • Other Ways to Give
      • Be a Corporate Partner
      • Donate Your Car
      • Give Stock
      • Make a Planned Gift
      • Create a Will
      • Donor Advised Funds
    • Fundraise
      • NHF GO
      • Run in a Marathon
      • 2022 United Airlines New York City Half Marathon
      • Create Your Own Fundraiser
      • Fundraise on Facebook
    • Join Us
      • Takeda Shoes
      • Red Tie Soiree
      • Bleeding Disorders Awareness Month
      • Find a Walk
      • For Young Professionals
NBDF’s Established Initiatives & Impact >

Wednesday Webinar Series

NHF's Wednesday Webinars are a free education series open to providers and community members. Register to attend and learn about the latest in research, breakthrough developments, and more.
Register for Wednesday Webinar Series
  1. Home
  2. Community Resources
  3. Request Information
  4. Wednesday Webinar Series
  • Burden on parents of children with moderate or severe von Willebrand disease: The impact of clinical data
    20 Sep

    Burden on parents of children with moderate or severe von Willebrand disease: The impact of clinical data

    Sep 20, 2023 - Sep 20, 2023
  • Rebrand webinar image
    13 Sep

    From NHF to NBDF: A Time for Change

    Sep 13, 2023 - Sep 13, 2023
  • HEMGENIX Patient Eligibility and Treatment Steps
    06 Sep

    HEMGENIX (etranacogene dezapavovec-drlb) Patient Eligibility and Treatment Steps

    Sep 6, 2023 - Sep 6, 2023
  • BDC 2023 Sneak Peek
    09 Aug

    BDC 2023 Sneak Peek

    Aug 9, 2023 - Aug 9, 2023
  • Sanofi August 2 webinar
    02 Aug

    Factor up: Discover the Possibility of Higher Factor VIII Levels for Longer

    Aug 2, 2023 - Aug 2, 2023
  • The New WFH Shared Decision-Making Tool
    26 Jul

    The New WFH Shared Decision-Making Tool

    Jul 26, 2023 - Jul 26, 2023
  • Gene Editing
    19 Jul

    Gene Editing

    Jul 19, 2023 - Jul 19, 2023
  • Corporate Giving 101
    12 Jul

    Corporate Giving 101

    Jul 12, 2023 - Jul 12, 2023
  • Hemophilia Gene Therapy: First, Do No Harm
    14 Jun

    Hemophilia Gene Therapy: First, Do No Harm

    Jun 14, 2023 - Jun 14, 2023
  • Managing Pregnant Women with Hemophilia and von Willebrand Disease: How Do We Provide Optimum Care and Prevent Complications?
    07 Jun

    Managing Pregnant Women with Hemophilia and von Willebrand Disease: How Do We Provide Optimum Care and Prevent Complications?

    Jun 7, 2023 - Jun 7, 2023
  • Learn More About HEMABiologic’s Latest Treatment Option for the Hemophilia Community
    31 May

    Learn More About HEMABiologic’s Latest Treatment Option for the Hemophilia Community

    May 31, 2023 - May 31, 2023
  • The Evidence for Shared-Decision Making for Hemophilia Gene Therapy
    24 May

    The Evidence for Shared-Decision Making for Hemophilia Gene Therapy

    May 24, 2023 - May 24, 2023
  • Gene Therapy: Breakthrough Era for Hemophilia B. Introducing Hemgenix ®️ (Etranacogene Dezaparvovec-Drlb)
    17 May

    Gene Therapy: A Breakthrough Era for Hemophilia B. Introducing Hemgenix®️ (Etranacogene Dezaparvovec-Drlb)

    May 17, 2023 - May 17, 2023
  • Recombinant Factor VIII FC Fusion Protein for First-time Immune Tolerance
    10 May

    Recombinant Factor VIII FC Fusion Protein for First-time Immune Tolerance

    May 10, 2023
  • Lentiviral Gene Therapy for Artemis-Deficient SCID
    03 May

    Lentiviral Gene Therapy for Artemis-Deficient SCID

    May 3, 2023 - May 3, 2023
  • Wednesday Webinar: Increasing Health Equity IQ
    26 Apr

    Increasing Health Equity IQ

    Apr 26, 2023 - Apr 26, 2023
  • Wednesday Webinar: 10 Things You Need to Know About Cannabis
    19 Apr

    10 Things You Need to Know About Cannabis

    Apr 19, 2023 - Apr 19, 2023
  • Raising the Bar for Joint Health
    12 Apr

    Raising the Bar for Joint Health

    Apr 12, 2023 - Apr 12, 2023
  • Empowering the Community Through Knowledge and Resources
    05 Apr

    Empowering the Community Through Knowledge and Resources

    Apr 5, 2023 - Apr 5, 2023
  • National Research Blueprint: A Continued Conversation
    29 Mar

    National Research Blueprint: A Continued Conversation

    Mar 29, 2023 - Mar 29, 2023
  • National Research Blueprint: An Introduction
    22 Mar

    National Research Blueprint: An Introduction

    Mar 22, 2023 - Mar 22, 2023
  • Global perspectives on prophylaxis
    15 Mar

    Global Perspectives on Prophylaxis

    Mar 15, 2023 - Mar 15, 2023
  • Gene therapy in hemophilia: educating the community on the science to aid in conversation with your healthcare team
    08 Mar

    Gene Therapy in Hemophilia: Educating the Community on the Science to Aid in Conversation with Your Healthcare Team

    Mar 8, 2023 - Mar 8, 2023
  • Equitable Access to Behavioral Health Treatment for the Bleeding Disorders Community
    01 Mar

    Equitable Access to Behavioral Health Treatment for the Bleeding Disorders Community

    Mar 1, 2023 - Mar 1, 2023

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