IDFNZ Kids Foundation - Helping Kiwis with Rare Diseases of the Liver and Immune System (PID)

This Rare Disease Day (Sunday 28th of February), we are asking for donations and support to help the Rare Gems in our community - children, teenagers and adults with diagnosed Primary Immune Deficiency (PID) disorders as well as bone marrow and liver transplant children.

People living with rare diseases often have complex needs and face unique challenges. The current health system is often difficult for these families to navigate.

IDFNZ Kids Foundation provides emotional, financial and medical specialist support as well as offering hospital advocacy and funding research. We offer practical advice and an open door to our extended community of families.

IDFNZ Kids Foundation is a non-profit organisation dedicated to supporting children, teenagers and adults with diagnosed Primary Immune Deficiency (PID) disorders as well as bone marrow and liver transplant children. We are a charitable foundation that appreciates any donations to ensure kids are getting the support and help they deserve.

IDFNZ has a proven track record of over 31 Years supporting and uplifting New Zealand PID / Transplant children dealing with life-threatening medical conditions.

Visit www.idfnz.org.nz to read some of our current patient stories and learn more about our work with this special needs patient community.