Be an advocate for yourself, your patients, and your community by learning about this complex disease.


Request Informational Booklets

Education Is Key.

Are you a patient just learning about your antibodies? Start here for an introduction to what is happening in your body.

Start Here

Provider Resources.

Are you a provider looking for the most current, evidence-based guidelines for the management of alloimmunized pregnancies?

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Ways You Can Help

Current Research and Clinical Trials

Understand The Terminology

Test Your Allo Knowledge

We have a growing resource library.

Point of Care Materials

Point of Care Materials

AHF is happy to provide free booklets to women and health care providers dealing with HDFN. These booklets contain an HDFN overview, monitoring and treatment options, and spots for patients to record their values. Click here to request your copies today.

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Participate in Research

Participate in Research

The Allo Hope Foundation and AllStripes are partnering to create a database that will enable multiple Alloimmunization & HDFN research projects! We’re looking for patients/families willing to contribute their de-identified medical records to make this effort as strong as possible. Your medical journey can accelerate the development of new treatment and monitoring methods for alloimmunization & HDFN. Because these are rare conditions, researchers need more information directly from patients and their families to fully understand the condition.

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Prenatal Decision Tree

Prenatal Decision Tree

The Prenatal Decision Tree can be used as a step by step guide through the proper course of prenatal care for alloimmunized patients according to current medical literature. If your care plan differs from this, discuss it with your physicians and seek a second opinion if needed. For additional references and a more in-depth explanation of the information in this tree, please see our Providers page.

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Allo Stories

Journey with our families as they go through pregnancy dealing with alloimmunization and HDFN.

Disclaimer: The purpose of this website is to provide general education, access to resources, and relevant literature. This website does not provide specific medical advice or recommendations for individual patients and is not a substitute for speaking with qualified healthcare professionals. The Allo Hope Foundation strongly recommends that care and treatment related to alloimmunization and HDFN be made in consultation with your physicians who are familiar with your individual health situation.

The Allo Hope Foundation - Protecting babies, supporting families.

  • We Are Here To Help.

    We want to connect you with the latest alloimmunization & HDFN information. Let us know what you need as a member of the alloimmunized community. Do you need additional resources or information? Would you like copies of our point of care materials and patient handouts? Email us and let us know how we can serve you. You can also join our quarterly newsletter to stay informed on current developments in the alloimmunization & HDFN world.

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Mission Statement

Our mission is to prevent any harm, stillbirth or infant death caused by alloimmunization and HDFN. We are dedicated to providing patient advocacy, support and education while promoting research and improving healthcare practices for the condition.