Newly Diagnosed

XLA Life exists to welcome patients and families into a supportive community with resources and information. If you or a loved one was recently diagnosed with X-Linked Agammaglobulinemia (XLA), here are a few immediate things you need to know.

1) You are not alone.

- The incidence rate in the USA alone is 1 in every 190,000 male births.

- Many families have gone through generations with XLA

- Fill out the form below to Join the XLA Life family and get in touch with others

MAKE A LINK TO THE JOIN OUR FAMILY FORM

2) Suggested Resources: as we continue to organize resources for the newly diagnosed, read the following links from our friends at the Immune Deficiency Foundation.

- Learn about XLA here

- Join the XLA Families Facebook page

3) Introduction to XLA