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The Immune Deficiency Foundation is the national patient organization dedicated to improving the diagnosis, treatment and quality of life of persons with primary immunodeficiency diseases through advocacy, education and research.
IDF provides accurate and timely information for patients and families living with PI and offers valuable resources. IDF...
- Helps the patient and medical community gain a broader understanding of PI through education and outreach efforts;
- Promotes, participates in, and conducts research that has helped characterize PI and given patients and physicians substantially improved treatment options;
- Addresses patient needs through public policy programs by focusing on issues such as insurance reimbursement, patient confidentiality, ensuring the safety and availability of immunoglobulin therapy, and maintaining and enhancing patient access to treatment options.
Thousands of individuals and families affected by PI diseases depend on IDF for advocacy, education and empowerment.