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Patients with primary immunodeficiency diseases have rights, especially in terms of treatment and standards of care. (Click here for IDF’s Bill of Rights for Patients with PI.) To help patients protect those rights and educate healthcare providers and/or insurance companies, the American Academy of Allergy, Asthma & Immunology (AAAAI) Primary Immunodeficiency Diseases (PID) Committee created an IVIG toolkit. The kit includes recommendations and guidelines for physicians and for those responsible for coverage determinations to ensure the safe, effective and appropriate use of IVIG. You can share these documents with your healthcare provider and/or insurance company. The IVIG toolkit includes: