Useful information about APDS to share with your family and doctor.
Use this worksheet to record your family’s health history.
Learn more about APDS, a genetic condition that may affect your children and extended family.
Heather is the mom of an amazing 10-year-old daughter who was diagnosed with the rare primary immunodeficiency, APDS. This is her story.
This video highlights the variety and severity of symptoms that each person with APDS may experience, and the importance of genetic testing.
This video, produced by ‘The Balancing Act’, a Lifetime show, features Tyler and Kaitlyn, a brother and sister who have been diagnosed with APDS.
A podcast for patients on the importance of their role in clinical trials, hosted by the Immune Deficiency Foundation (IDF).
Listen via Soundcloud
Listen via YouTube
Hosted by Elaine Kulm, a Nurse Practitioner with Kristin, a patient who was diagnosed with APDS as an adult. This podcast represents one person’s experience and should not be considered as medical advice.
Hosted by Dr Hajjar, a Clinical Immunologist and Allergist, with special guest – Megan, a patient with PI. This podcast represents one person’s experience and should not be considered as medical advice.
