The HFMD is a non-profit organization dedicated to providing programs and services for those living with hemophilia and related genetic bleeding disorders. Read more »
Let your voice be heard and tell your story! Join HFMD and other bleeding disorder community members for the 2020 Bleeding Disorder & Rare Disease Day at the Minnesota State Capitol on Friday, March 20th. Meet with your elected officials during the day to inform them of the importance of good health care for everyone! Join us for an Advocacy Workshop from 11:00 a.m. for tips and talking points on speaking to your representative. Then join us for a rally in the Capitol rotunda at 1:30 p.m. Visit the Events Tab above for more information on how to register for this event.
Red Caps for Hemophilia Scrapbook from 1969 through 1994: Red Caps Scrapbook