Our vision is to help find a cure for Job Syndrome by providing the scientific community with additional opportunities to further research the disease.

The APS Type 1 Foundation exists to drive research to improve the lives of people with this rare disease, and ultimately find a cure. We support education, awareness and fundraising for critical research in APS Type 1.

The IPEX Foundation's mission is to improve the treatment, quality of life, and long-term outlook for children and adults living with IPEX syndrome through research, support, education, and advocacy to families and patients.

XLA Life fosters the unification and empowerment of the global X-Linked Agammaglobulinemia (XLA) community through education, advocacy, and initiatives that aim to improve the overall quality of life for those affected by XLA.