Take a look at what our rare disease nonprofit has accomplished since its establishment in 2019:
Take a look at what our rare disease nonprofit has accomplished since its establishment in 2019:
Evidence-based resources for both patients and clinicians, empowering informed care and decisions.
Supporting global awareness, education, and resources through impactful fundraising initiatives, in partnership with organizations making a difference
Active and engaged social media community across Instagram, Facebook, LinkedIn, and YouTube.
Expanding global outreach to developing countries with limited access to Rh Immune Globulin and comprehensive care for HDFN.
Providing ongoing peer-to-peer support for our network of 2,000 alloimmunized patients through our online support group
March 12th is now officially recognized as World Alloimmunization and HDFN Awareness Day.
Traveling, exhibiting, and speaking at key conferences such as SMFM, ACOG, AABB, ISBT, THOR, and more.
JOIN THE FIGHT
There are plenty of ways to get involved with The Allo Hope Foundation including sharing your story, participating in research, donations and more.
©2025 ALLO HOPE FOUNDATION. All Rights Reserved. All trademarks are the property of their respective owners. The Allo Hope Foundation is a qualified 501(c)(3) tax- exempt organization EIN: 84-2785519. - Download Form 990
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.