Resources
Dive into available resources designed to help you navigate through an APDS diagnosis and treatment with Joenja.

Tyler, Tyrek, Twana, Liam, Annie

Downloadable resources
For people exploring Joenja as a treatment option

Patient brochure
Learn more about Joenja results and dosing.

Physician locator tool
Connect with physicians who are knowledgeable about diagnosing, managing, and treating APDS.
For those taking Joenja

Joenja leaflet
Learn more about what to expect after getting Joenja prescribed.

APDS Assist enrollment form
Complete the enrollment form below and submit it to APDS Assist.

APDS Assist brochure
Learn how you can take advantage of APDS Assist.

Administration guide
Learn how to take Joenja, and tips for staying on treatment.
For those exploring genetic testing

Family discussion brochure
Learn more about APDS as a genetic condition and how it may impact other members of your family.

What to expect with genetic testing
Download this informative guide on what to expect from genetic testing and office visits.
Stay in touch
Sign up for emails to get the latest news and stay up to date on everything Joenja.

Patient advocacy
Having a rare disease can be hard. You may even feel alone because you don’t know many people like you, but there are hundreds of people in the United States living with APDS.
Click on each logo to learn more about each patient advocacy group dedicated to people with primary immunodeficiencies, APDS, and their families.
APDS, activated PI3K delta syndrome.
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