The National Bleeding Disorders Foundation (NBDF) proudly announces that our former President and CEO, Leonard A. Valentino, MD, has been appointed as President of WFH USA. This appointment represents an exciting expansion of Doctor Valentino's dedication to the bleeding disorders community, now on a global scale.
During his impactful tenure at NBDF, Leonard Valentino led transformative initiatives that strengthened our foundation's research programs, enhanced patient support services, and advanced crucial advocacy efforts. His leadership was instrumental in our successful transition from the National Hemophilia Foundation to the National Bleeding Disorders Foundation, reflecting our expanded commitment to serving all those affected by inherited blood and bleeding disorders.
"We are thrilled to see Dr. Valentino's expertise and passionate advocacy extend to the global bleeding disorders community through WFH USA," said Ryan Griffith, NBDF Board Chair. "His appointment strengthens the connections between our organizations and amplifies our shared mission of improving care for all people with bleeding disorders."
In his new role at WFH USA, Dr. Valentino will lead efforts to advance global access to treatment through partnerships with American residents, foundations, and corporations. WFH USA works alongside corporate and community partners, patient organizations nationwide, and dedicated individuals to pursue its vision of Treatment for all people with bleeding disorders worldwide.
For more articles about Dr. Leonard A. Valentino, see below:
About WFH USA
Since its founding in 1996, the WFH USA has advanced support for the global mission of the World Federation of Hemophilia (WFH) within the United States. WFH USA, a 501(c)3 organization, provides American residents, foundations, and corporations a charitable opportunity to help ensure "Treatment for All" for people with bleeding disorders all over the world.
About the National Bleeding Disorders Foundation
The National Bleeding Disorders Foundation (NBDF) is dedicated to finding cures for inheritable blood and bleeding disorders and addressing and preventing these disorders' complications through research, education, and advocacy, enabling people and families to thrive. Today, NBDF serves people across the United States with all bleeding disorders, including hemophilia, von Willebrand disease, rare factor deficiencies, and platelet disorders. The foundation also supports a network of 50 chapters across the country. To learn more, visit www.bleeding.org and follow NBDF across social media @nbd_foundation.
Written by: Kyla Clark, Director of PR and Communications
