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Comunicado de prensa: HFA organiza el primer intensivo de promoción

FOR IMMEDIATE RELEASE:     October 20, 2009

 Washington, DC:  The Hemophilia Federation of America (HFA) held its first Advocacy Intensive weekend October 2 – 5, 2009.  The program is a best practice model for bringing HFA social advocacy programs full circle and encouraging members of the bleeding disorders community to reach their  full potential through role modeling and self advocacy.

 “It was a wonderful group to work with. The participants were eager to learn and we applaud their determination and enthusiasm to become dedicated community advocates,” states Kisa Carter, HFA’s Public Policy Director. 

 All participants expressed appreciation for the opportunity to become stronger advocates for the bleeding disorders community. One participant stated, “The name ‘Intensive’ is clearly appropriate.  From start to finish, the weekend was incredibly planned and full of useful information and experiences.” Feedback from another participant commends the HFA for an invitation to “a valuable learning tool in advancing [my] abilities as a community advocate.” 

 The program is delivered during an intense three to five days of experiential learning where participants engage in a variety of hands-on activities including team building and communication exercises, special projects and training on the legislative process.  The participants also authored their own “Personal Story” and delivered it to legislators on Capitol Hill.       

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La Hemophilia Federation of America es una organización nacional 501(c)(3) que consta de 30 organizaciones miembro y numerosos miembros individuales que ofrecen asistencia y defensa de base en nombre de la comunidad de trastornos de la coagulación. Constituida en 1994, la HFA ofrece programas y servicios para mejorar la calidad de vida de personas con hemofilia y enfermedad de von Willebrand (EVW).

Para obtener más información, visite nuestro sitio web en www.hemophiliafed.org o llame al 1-800-230-9797.

CONTACTO DE HFA:  Susan Swindle, Development Director |713-203-8548| s.swindle@hemophiliafed.org

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