NMDP is a global nonprofit leader in cell therapy, helping save the lives of patients with blood cancers and disorders. Since our founding in 1987, the world has evolved—and so have we. Throughout the years, we’ve been known by many names, including the National Marrow Donor Program® and Be The Match®. 

The Infusion Nurses Society (INS) is dedicated to exceeding the public’s expectations of excellence by setting the standard for infusion care. Membership is open to nurses and health care professionals from all practice settings who are involved in or interested in the specialty practice of infusion therapy.

Immunoglobulin Nursing Society (IgNS) is a professional organization dedicated to nursing professionals in education, management, practice and research in the field of immunoglobulin (Ig) therapy.

The Federation of Clinical Immunology Societies (FOCIS) exists to improve human health through immunology by fostering interdisciplinary approaches to both understand and treat immune-based diseases.

The mission of the Clinical Immunology Society (CIS) is to facilitate education, translational research and novel approaches to therapy in clinical immunology to promote excellence in the care of patients with immunologic/inflammatory disorders.

The American Academy of Pediatrics (AAP) is a professional organization for pediatricians. It is committed to the attainment of optimal physical, mental, and social health and well-being for all infants, children, adolescents, and young adults.

The American Academy of Allergy, Asthma & Immunology (AAAAI) is the leading membership organization of more than 7,100 allergists / immunologists and patients' trusted resource for allergies, asthma and immune deficiency disorders.

The XLP Research Trust promotes and funds research into the cause, management, symptoms and cure for X-linked lymphoproliferative (XLP) disease; raises awareness of the disease; and is a point of contact and support for families affected by XLP.

The Wiskott-Aldrich Foundation is a volunteer run, non-profit organization, dedicated to funding research to find improved cures for Wiskott-Aldrich Syndrome, and to support for families living with the disease around the world. We are a group of passionate individuals, each with our own area of expertise, with a common mission to help families and patients with WAS.

At the SCID Foundation, our mission is to empower families affected by Severe Combined Immunodeficiency (SCID) through awareness, education, advocacy, and support.