March 28, 2005
National Hemophilia Foundation Returns to the Hill

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Women's Bleeding Disorders - von Willebrand's Disease
First Steps
National Prevention Program

NHF Youthworld

Come Join us at our 57th Annual Meeting!

The National Hemophilia Foundation's 57th Annual Meeting
October 27 to 29, 2005
San Diego Marriott Hotel and Marina, San Diego, CA

Network with other families, colleagues and industry representatives. Socialize at fun events. Learn from the nation's leading experts. Register online by June 30, and save 15%!

Find out more >>


Please join us at the second annual NHF National Youth Leadership Institute--a special program for young adults.

Apply by July 31, 2005 >>

 


Celebrating Leadership: Chapters Make It Happen

The National Hemophilia Foundation is pleased to present our Fifth Annual Gala, which will take place on Saturday, June 4, 2005, at The Lighthouse, Pier 61, located on the Hudson River in Manhattan. This year's gala theme is "Celebrating Leadership: Chapters Make It Happen." Please join us for a festive evening of cocktails, dinner and dancing, as we celebrate the outstanding leadership of all our chapters.

For details and sponsorship opportunities, please click here >>


Scholarships for Students
with Bleeding Disorders

Kevin Child Scholarship
Each year a $1000 Kevin Child Scholarship is awarded to a qualified individual in memory of Kevin Child.
Find out more >>


Project Red Flag Academic Scholarship for
Women with Bleeding Disorders

This scholarship is designed to benefit women with bleeding disorders in their pursuit of post high school studies. Two $2500 scholarships are available.
Find out more and download application >>


View all available scholarships
Over twenty non-NHF affiliated scholarships are listed on our web site.
Visit our scholarship listings>>


It's Time for a Cure for Bleeding Disorders

NHF has launched a new tool to help you get involved and raise needed funds for the It’s Time for a Cure campaign! In just four simple steps, you can create a personalized Web page on NHF’s Web site to e-mail to all your friends and family, who can contribute to your fundraising goal and help us all get that much closer to a cure!

To find out more about It's Time for a Cure, click here >>

To find out how to create your personal fundraising webpage, click here >>



NHF Discussion Groups for Bleeding Disorders Community
Online Discussion Groups
Ask questions, exchange ideas and share your stories in our discussion groups.

Join one of the following discussion groups:

Read more about NHF's Discussion Groups >>



NHF Online Inhibitors Community
Inhibitors Online Community

Find out the latest information on Inhibitors, in our new Online Community which also previews the look-and-feel of the newly redesigned NHF website.

Read More >>



National Hemophilia Foundation
116 West 32nd Street, 11th Floor
New York, NY 10001
(800) 42-HANDI - (212) 328-3700 - fax (212) 328-3777
Email: info@hemophilia.org
HANDI Information Service: handi@hemophilia.org

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