HFA News & Notes

WFH appoints John Bournas as new CEO/ ED

Click for link to WFH Montreal, Canada, January 10, 2012 — The World Federation of Hemophilia is pleased to [...] Read More >>

U.S. Department of Health and Human Services releases Essential Health Benefits Bulletin

On Monday, Dec. 16, the U.S. Department of Health and Human Services (HHS) released a bulletin outlining guidance [...] Read More >>

BAXTER: PHASE I TRIAL OF LONGER-ACTING RECOMBINANT FVIII

Link to Baxter’s Press Release BAXTER INITIATES PHASE I CLINICAL TRIAL OF LONGER-ACTING RECOMBINANT FVIII [...] Read More >>

Contact Info

Hemophilia Federation of America
210 7th St. SE, Suite 200B
Washington D.C., 20003
800.230.9797
202.675.6984
202.675.6983

© 2011 Hemophilia Federation of America · Board of Directors Only · BB Admin Only · Privacy & Legal

PRESS RELEASE: HFA AWARDED CDC COOPERATIVE AGREEMENT FOR FIT FACTOR PROGRAM

FOR IMMEDIATE RELEASE: September 1, 2009

The Hemophilia Federation of America (HFA), a national nonprofit headquartered in Washington, DC, has been awarded a five-year cooperative agreement from the Centers for Disease Control and Prevention (CDC).  The award supports a program aimed at promoting physical activity and maintaining a healthy weight in individuals with hemophilia.

 Proper nutrition, combined with safe and effective exercise, is especially important to facilitate good health in people with hemophilia. The program, Fit Factor:  Strength, Flexibility and Wellness, offers services designed to improve health, fitness, and quality of life through regular physical activity and proper nutrition. The program will offer video podcasts, support in tracking physical activity, and dietary meal plans based on age, weight and medical complications secondary to hemophilia for those unable to afford health club memberships or have personal or travel constraints due to physical limitations or rural locations. 

 Chad Steven, HFA President, states, “We are extremely proud of the cooperative agreement with the CDC for Fit Factor.  The program is strategically aligned with HFA’s goal of improving the quality of life for all community members, and we are pleased to be able to offer this program to meet the needs of our community members.”

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The Hemophilia Federation of America is a national 501(c)(3) organization consisting of 30 member organizations and numerous individual members who offer assistance and grassroots advocacy on behalf of the bleeding disorders community.   Incorporated in 1994, the HFA provides programs and services to improve the quality of life for persons with hemophilia and von Willebrand disease (VWD). For more information, visit our website at www.hemophiliafed.org or call 1-800-230-9797.

 

HFA CONTACT:  Susan Swindle, Development Director

Phone: 713-203-8540     Email: s.swindle@hemophiliafed.org