Useful information about APDS to share with your family and doctor.
Use this worksheet to record your family’s health history.
A reference for frequently asked questions about APDS.
A useful guide to help understand terms you may hear from your doctor or find in your research.
A helpful resource for people living with APDS, and their support network.
What is happening in my body?
Dr Eveline Wu talks through the patient journey to a diagnosis.
Dr Hartog talks about the genetics behind APDS and how it’s diagnosed.
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.
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.