The checklist includes tips for creating a family emergency plan that addresses both universal needs and special considerations for those affected by a bleeding disorder.
The National Hemophilia Foundation's (NHF's) publications contain informative resources for people with bleeding disorders and their families. These publications will be of use to healthcare providers, educators, librarians and other healthcare organizations.
Several of these NHF publications may also be available in bulk quantities. For more information about placing a “reasonable” request for copies in bulk, or for help with finding additional materials not listed here, please contact HANDI, at firstname.lastname@example.org or via phone at 800-42-HANDI. (Be sure to include your name, mailing address, and daytime phone number in any e-mail requests.)