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American Indian Health Service of Chicago Inc
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The Paisley Foundation Inc
Raise awareness of Thanatophoric Dysplasia, financially support clinical research, and provide financial assistance and community resources to affected families Raise Awareness of Thanatophoric Dysplasia Financially Support Clinical Research and Provide Financial Assistance and Community Resources to Affected Families Building a Community to Support TD Families The foundations purpose is to raise awareness of Thanatophoric Dysplasia TD financially assist families both in their everyday lives and where insurancesocial programs fall short and to be a community resource for families present and future whose children have TD.
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Gift Distribution
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Pascales Pals Inc
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Professional Societies & Associations
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Down Syndrome Medical Interest Group
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Riaan Research Initiative Inc
501(c)(3) non-profit organization hunting for a cure for rare and life-limiting genetic diseases that hurt children, starting with Cockayne syndrome.
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Oakland Gardens
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Ichoose Foundation Inc
OUR MISSIONTo serve women going through cancer treatment or during post treatment by providing products and services to help them feel beautiful strong and empowered.
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International Association of Sickle Cell Nurses and Physician ASSISTAN
International Association of Sickle Cell Nurses and Professional Associates IASCNAPA PROVIDES A PLATFORM FOR NURSES, NURSE PRACTITIONERS, PHYSICIAN ASSISTANTS SOCIAL WORKERS, SICKLE CELL ADVOCATES, AND OTHER HEALTHCARE PROFESSIONALS CARING FOR INDIVIDUALS WITH SICKLE CELL DISEASE TO IMPROVE THE CARE OF PEOPLE WITH SICKLE CELL DISEASE Home Who We Are Membership Scholarships Events Contact More Join us in the fight against Sickle Cell Disease We are dedicated nurses and professionalassociates striving to improve the lives of Sickle Cell Warriors.
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Specifically Named Diseases
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YBRP Inc
YBRP is a non-profit organization whose mission is to positively impact the lives of individuals with HNRNPH2 genetic variations.
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Health - General & Rehabilitative N.E.C.
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4P-Support Group
Our mission is to serve our membership by providing information, education and support; uniting families, researchers, and professionals; and promoting awareness and understanding of 4p- syndrome, with Wolf-Hirschhorn Syndrome as the main condition, and the related 4th chromosome abnormalities.
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