NBDF Unveils THRIVE Campaign: Empowering Individuals with Bleeding Disorders through 6 Essential Steps

NBDF Unveils THRIVE Campaign: Empowering Individuals with Bleeding Disorders through 6 Essential Steps
The National Bleeding Disorders Foundation (NBDF) announces the THRIVE campaign to raise awareness and educate on living healthily with bleeding disorders. Discover six essential steps to empower individuals and families, offering resources to thrive daily.

NBDF Announces 2023 Kevin Child Scholarship Winner

NBDF Announces 2023 Kevin Child Scholarship Winner
The National Bleeding Disorders Foundation (NBDF) is pleased to announce that Hunter Montgomery of Cottonwood Heights, Utah was selected as the recipient of the 2023 Kevin Child Scholarship (KCS). Hunter, who has severe hemophilia A, is currently a 3rd year medical student at the University of Utah School of Medicine in Salt Lake City. His plans are to become a clinician-scientist working to improve the lives of his patients.

National Bleeding Disorders Foundation raises $200,000 at the most successful Red Tie Soiree to date.

National Bleeding Disorders Foundation raises $200,000 at the most successful Red Tie Soiree to date.
CHICAGO, Ill. — The National Bleeding Disorders Foundation (NBDF) painted the town red at its annual Red Tie Soiree at the Chicago Cultural Center on October 27. The signature fundraising gala raised over $200,000 for the inheritable blood and bleeding disorders community- the most money the event has ever raised.

Embracing Change and Empowering Communities: 2023 Bleeding Disorders Conference

Embracing Change and Empowering Communities: 2023 Bleeding Disorders Conference
The National Hemophilia Foundation (NHF) is thrilled to announce the highly anticipated 2023 Bleeding Disorders Conference, set to take place from August 17-19 at the renowned Gaylord National Resort & Convention Center in National Harbor, MD. This year's conference promises to be a groundbreaking event, bringing together individuals affected by inheritable blood and bleeding disorders, health care professionals, and industry experts.

NHF announces publication of working group recommendations as part of the National Research Blueprint for Inherited Bleeding Disorders

NHF announces publication of working group recommendations as part of the National Research Blueprint for Inherited Bleeding Disorders
Discover NHF's recent research recommendations for inherited bleeding disorders. Explore key issues and opportunities in advancing research.

NHF Announces Fall 2022 Wednesday Webinar Schedule

NHF Announces Fall 2022 Wednesday Webinar Schedule

FOR IMMEDIATE RELEASE                                                                                
Ilana Ostrin    
Senior Director of Public Relations and Communications   

National Hemophilia Foundation “Starts the Conversation” During Bleeding Disorders Awareness Month

National Hemophilia Foundation “Starts the Conversation” During Bleeding Disorders Awareness Month

Awareness month campaign encourages the community to raise their voices and share what is most important and relevant to their conditions throughout March.

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