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Home
  • Who We Are
    • 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
  • Subscribe
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MASAC Document 077 - Recommendation Regarding Neonatal Intracranial Hemorrhage and Postpartum Hemorrhage
Intracranial hemorrhage in the neonate with a bleeding disorder can cause permanent disability or death, especially if it is unrecognized and untreated. The incidence of intracranial hemorrhage in neonates with congenital bleeding disorders is…
MASAC Document 081 - Considerations for Developing Psychosocial Interventions for Women with Bleeding Disorders
This material is provided for your general information only. NHF does not give medical advice or engage in the practice of medicine. NHF under no circumstances recommends particular treatment for specific individuals and in all…
MASAC Document 087 - Recommendation on Plasma Transfusion Alternatives
Human plasma is required to correct the hemostatic defect in patients with rare hereditary coagulation deficiencies, such as factors I, II, V, VII, X, XI and XIII, for which specific therapeutic concentrates are not available. Plasma is also…
MASAC Document 091 - Recommendation Regarding Risk of Germline Transmission in Gene Therapy Trials for Hemophilia
The National Hemophilia Foundation supports gene therapy as the most promising strategy for curing hemophilia. At this time, NHF also supports the position advocated in the Orkin-Motulsky report on gene therapy that gene therapy should be somatic…
MASAC Document 099 - Resolution on Creutzfeldt-Jakob Disease, New Variant CJD, and Plasma-Derived Coagulation Products
Introduction Creutzfeldt-Jakob disease (CJD) is a rare but fatal condition associated with a poorly understood transmissible agent that may arise from genetic mutations in the prion protein gene or may be contracted through…
MASAC Document 102 - Recommendation Regarding the Need for Collaborative Effort to Collect Data Regarding Interventions to Prevent Joint Damage Secondary to Hemophilia
Progressive joint destruction contributes major morbidity to persons with hemophilia. Currently, there are multiple approaches to prevent or ameliorate early joint inflammation (synovitis) including prophylaxis (regular replacement factor infusions…
MASAC Document 109 - Resolution Concerning Participation in AIDS Clinical Trials by HIV-Infected Persons with Bleeding Disorders
MASAC supports participation in AIDS clinical trials by HIV-infected persons with hemophilia and other bleeding disorders. MASAC specifically supports the optimization of inclusion criteria to allow such individuals to participate in AIDS clinical…
MASAC Document 110 - Recommendation Concerning CMV Screening of Blood Products for Use in HIV-Positive Individuals with Hemophilia
CMV-seropositive blood donors may have peripheral blood mononuclear cells that are latently infected with CMV. Furthermore, a small proportion of CMV-seronegative individuals are CMV carriers who are able to transmit CMV through blood products for…
MASAC Document 111 - Resolution Concerning the Development of Comprehensive Outcome Measures
The National Hemophilia Foundation (NHF) supports the development of comprehensive outcome measures for the treatment of bleeding disorders and their complications, with the goal of improving the quality of care for individuals with congenital…
MASAC Document 113 - Recommendations on Improved Access to Emergency Medical Care for Persons with Inherited Bleeding Disorders
MASAC has received reports of individuals with bleeding disorders who have experienced difficulties receiving appropriate emergency medical care. To address this issue, MASAC recommends the following: 1. Individuals with bleeding disorders should…

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