OUR VISION
We See a Future Free of Bleeding Disorders
We are a nonprofit organization devoting its efforts to improving the quality of life for persons affected with bleeding disorders and their complications. This mission is accomplished through outreach development, educational programs, informational literature, support services and patient referrals. HFM is a proud member of the Hemophilia Federation of America.
**Important Announcement**
As funding becomes increasingly limited, we must recognize the specialty pharmacies that partner with HFM and financially support our mission. Their partnership and contributions enable us to host events and programs such as Summer Camp, the Milton Doug Hiteshew Scholarship Program, Patient Service Support, Infusion Workshops, Patient Advocacy, Family Educational Programming, Family Weekend, Women’s Support Group Meetings, Men’s Support Group Meetings, and much more. We strongly encourage you to support the companies listed below and
About This Website
HFM wants to help ...
Through advocacy, education, outreach development, support services and the relentless pursuit of a cure, we aim to improve the lives of individuals in Maryland affected by hemophilia, vWD and other bleeding disorders.
Hemophilia Foundation of Maryland (HFM)
13 Class Court Parkville, MD 21234
Who we are
The Hemophilia Foundation of Maryland evolved in the early 1950’s from a group of concerned families who were affected by a hemophilia diagnosis.
These early chapter families were brought together by the social worker at St. Agnes Hospital, where most were treated. Some of the founding members of this organization continue to guide HFM today.
OUR VISION
We See a Future Free of Bleeding Disorders
We are a nonprofit organization devoting its efforts to improving the quality of life for persons affected with bleeding disorders and their complications. This mission is accomplished through outreach development, educational programs, informational literature, support services and patient referrals. HFM is a proud member of the Hemophilia Federation of America.Click a section below to begin ...
Through advocacy, education, organization and the relentless pursuit of a cure and increased research funding, we aim to improve the lives of individuals in Maryland affected by hemophilia, vWD and other bleeding disorders.
Ask Ally #6
Dear Ally, We just received a notice that our insurance will no longer cover my son’s preferred brand of clotting factor. They are asking us to switch to a different brand, but we’re concerned about how this might affect his treatment. What can we do?
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