October 3-5, 2025

National Conference for Women with Hemophilia and Rare Factor Deficiencies

NATIONAL CONFERENCE FOR WOMEN WITH HEMOPHILIA AND RARE FACTOR DEFICIENCIES

SAVE THE DATE! October 3-5, 2025
Hosted in-person
The Westin Detroit Metropolitan Airport

ELIGIBILITY

Conference attendance is open to women 18+ with hemophilia A, B, or rare factor deficiencies (1, 2, 5, 7, 10, 11, and 13; excluding factor V Leiden), including carriers with symptoms.

Applying does not guarantee in-person selection, as we must consider multiple factors, including diverse representation of states, the number of first-time attendees, and funding capacity.Ā 

”Las hispanohablantes son bienvenidas a nuestra conferencia! Muchas de nuestras sesiones serÔn interpretadas simultÔneamente para que todas podamos participar juntas.

CONFERENCE DETAILS

  • Women who are eligible to join our special three-day conference will learn from national experts and health care providers, connect with speakers and other attendees, and build community and connection.

Featuring educational sessions on:

  • Navigating Bleeds
  • Iron Deficiency
  • Rare Factor Deficiencies
  • Peri-Menopause & Menopause
  • OB-GYN Care
  • Sexual Health & Relationships
  • Research Updates

Plus, more time for small group discussions with a Leader in Action (LIA)!

There is NO CHARGE for this conference – transportation, hotel, and meals are provided for attendees.

The following expenses will be covered for eligible attendees during the conference: round-trip transportation, hotel accommodations, and meals.Ā 

Please note, the following expenses are not covered and will be the responsibility of the attendee: parking in your hometown, baggage handling fees, and meals and snacks during travel to and from the conference.

Application opens July 11 at 12:00pm

Thank you to our Sponsors

Presenting Sponsor
Community Lead Sponsor
Community Sponsors
Event Sponsor
Regional Supporter
Chapter Education Supporter
Community Supporters
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About Us

The Hemophilia Foundation of Michigan strives to improve the quality of life for all people affected by hemophilia, von Willebrand disease, other coagulation disorders, and related complications.

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