We are dedicated to helping children and adults with suspected or diagnosed Primary Immune Deficiencies (PID) as well as bone marrow and liver transplant children.
Our Foundation provides emotional, financial and medical specialist support as well as offering hospital advocacy and funding research into PID and liver disease. We offer practical advice and an open door to our extended community of families.
How can we help you? »We are a non-profit charity receiving no government funding to provide our services. This means we are reliant on the generosity of individuals, schools, corporates and trusts who are willing and able to support us.
We run annual fundraising programmes and events, but there are so many other ways you can help, including volunteering your time or providing 'gifts of joy' for our children.
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Our annual ALL4Good appeal is your chance to get involved and support our precious children.
All funds raised go towards ongoing support services for our families, such as much needed vouchers to cover the expenses of meals, pharmacy needs and petrol for our families who are often living in hospital for weeks or months on end.
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We proudly support people with PID disorders as well as bone marrow and liver transplant children.
We are eternally grateful to the ongoing support and generosity shown by our wonderful sponsors.
Meet our courageous families who take each day as it comes as they face big and small challenges.
Newborn screening for primary immunodeficiency disorders More good news for Australasian PID community !IDFNZ is thrilled that newborn screening has recently commenced in Australia. Screening for all New South Wales (NSW) newborns for the most severe forms of primary immunodeficiency (PID) disorders commenced on 1 August 2018. The aim is to ...
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