The more you understand about primary immunodeficiency (PI), the better you can live with the disease or support others in your life with PI. Learn more about PI, including the various diagnoses and treatment options.
Living with primary immunodeficiency (PI) can be challenging, but you’re not alone—many people with PI lead full and active lives. With the right support and resources, you can, too.
Be a hero for those with PI. Change lives by promoting primary immunodeficiency (PI) awareness and taking action in your community through advocacy, donating, volunteering, or fundraising.
Whether you’re a clinician, researcher, or an individual with primary immunodeficiency (PI), IDF has resources to help you advance the field. Get details on surveys, grants, and clinical trials.
Severe combined immune deficiency (SCID), also known as the bubble boy disease, is a rare, serious disorder where a child lacks the ability to fight off infections. Babies with SCID are placed in isolation both before and after the corrective treatment to protect them or isolate them from germs that could make them sick.
Riley’s parents share their perspectives on her diagnosis, treatment, and isolation. Her story of survival is one of many. Fortunately, many children with SCID are now grown, living healthy, productive lives. SCID can affect any infant, regardless of gender, race, ethnicity or socioeconomic status. Without appropriate early treatment, including the critical period of isolation, these babies cannot survive. Therefore it is essential that newborn screening for SCID is established in all 50 states because all babies, no matter where they are born, deserve a healthy life.
Browse IDF's video library to learn more about primary immunodeficiencies (PI) and the impact IDF has on people living with PI.
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The Immune Deficiency Foundation improves the diagnosis, treatment, and quality of life for every person affected by primary immunodeficiency.
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