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        <Desc>PATIENT SUPPORT - WE PROVIDE PATIENTS THROUGHOUT THEIR JOURNEY WITH ALLOIMMUNIZATION AND HDFN. THIS INCLUDES A LARGE PATIENT SUPPORT GROUP ON FACEBOOK WITH OVER 1,000 MEMBERS WORLDWIDE WHERE PATIENTS CAN CONNECT WITH OTHER WOMEN AND FIND ALL THE RESOURCES THEY NEED. WE ALSO MENTOR PATIENTS ONE ON ONE BY PROVIDING EMOTIONAL SUPPORT AND ANSWERING QUESTIONS THEY HAVE AND REFERRING THEM TO EXPERIENCED SPECIALISTS.</Desc>
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        <Desc>ADVOCACY AND AWARENESS - OUR ADVOCACY AND AWARENESS PROGRAM CONNECTS US WITH OTHER RELATED ORGANIZATIONS AND PATIENTS FROM ALL OVER THE WORLD. WE HELP BRING AWARENESS TO THE DISEASE THROUGH SPEAKING ENGAGEMENTS, PODCASTS, WEBINARS, BLOG POSTS, ETC. WE ALSO HELP RAISE SUPPORT FOR OUR PARTNER ORGANIZATION IN NIGERIA: RHESUS SOLUTIONS INITIATIVE.</Desc>
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        <Desc>RESEARCH - WE TEAMED UP WITH ALLSTRIPES TO CREATE A RARE DISEASE RESEARCH PROGRAM FOR ALLOIMMUNIZATION AND HDFN. THIS WILL HELP RESEARCHERS ADVANCE TREATMENTS FOR OUR DISEASE.</Desc>
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        <FormAndLineReferenceDesc>FORM 990 - ORGANIZATION'S MISSION</FormAndLineReferenceDesc>
        <ExplanationTxt>THE ALLO HOPE FOUNDATION'S MISSION IS TO PREVENT ANY HARM, STILLBIRTH OR INFANT DEATH CAUSED BY ALLOIMMUNIZATION (ALSO CALLED ISOIMMUNIZATION) AND HEMOLYTIC DISEASE OF THE FETUS AND NEWBORN (HDFN). WE ARE DEDICATED TO PROVIDING PATIENT ADVOCACY, SUPPORT, AND EDUCATION WHILE PROMOTING RESEARCH AND IMPROVING HEALTHCARE PRACTICES FOR THE CONDITION. CURRENTLY, WE ARE THE ONLY KNOWN 501(C)(3) ORGANIZATION FOUNDED TO OFFER RESOURCES AND SUPPORT GEARED SPECIFICALLY TOWARDS ALLOIMMUNIZED WOMEN AND HDFN PATIENTS.</ExplanationTxt>
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        <FormAndLineReferenceDesc>FORM 990, PAGE 2, PART III, LINE 4D</FormAndLineReferenceDesc>
        <ExplanationTxt>RESEARCH - WE TEAMED UP WITH ALLSTRIPES TO CREATE A RARE DISEASE RESEARCH PROGRAM FOR ALLOIMMUNIZATION AND HDFN. THIS WILL HELP RESEARCHERS ADVANCE TREATMENTS FOR OUR DISEASE.</ExplanationTxt>
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