NHF’s information resource center HANDI is ready to assist you! Now in its third decade, HANDI continues to be a trusted source of information and referrals for those affected by inheritable bleeding disorders and the general public.

Information specialists are adept at providing the latest resources on a wide variety of bleeding disorder-related topics, including but not limited to:

  • Hemophilia,
  • Von Willebrand disease,
  • Women and girls with bleeding disorders,
  • Rare factor deficiencies
  • School issues,
  • Aging issues,
  • Financial assistance
  • Gene therapy

HANDI has access to education and information resources in print, digital, and video formats, and provides referrals to healthcare providers and HTCs, local chapters, and to other support organizations based in the United States and abroad.

There are several easy ways to reach HANDI:

Call: 800.424.2634 (extension 2), 9am-5pm Eastern, Monday to Friday,

Email: handi@hemophilia.org

Submit an information request via HANDI’s online portal.

The HANDI Team looks forward to hearing from you!

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BioMarin Hemophilia Alliance Sanofi Genzyme