Kids with arthritis
deserve better
The Juvenile Arthritis Foundation Australia (JAFA) is dedicated to improving the lives of children and young people affected by juvenile idiopathic arthritis and related childhood rheumatic diseases.
Kids with arthritis
deserve better
The Juvenile Arthritis Foundation Australia (JAFA) is dedicated to improving the lives of children and young people affected by juvenile idiopathic arthritis and related childhood rheumatic diseases.
Kids with arthritis
deserve better
The Juvenile Arthritis Foundation Australia (JAFA) is dedicated to improving the lives of children and young people affected by juvenile idiopathic arthritis and related childhood rheumatic diseases.
Values
We strive to be innovative, agile, effective & efficient organisation that is sensitive and responsive to the needs of children with arthritis.
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Why is she so sad?
It's hard to learn when you're in pain
It's hard to be happy when you can't do what other kids do
It's hurtful when others tease because you're different
It's scary when you don't know what the future could hold for you
A day in the life…
How many kids do you know who have to go to a hospital on the way home from school to have an infusion?
Australian Juvenile Arthritis Registry (AJAR)
AJAR is a national registry of people aged 0-24 years with JIA and related CRDs. 713 children and young adults have now registered in AJAR. We are aiming to reach 1,000 by the end of 2025.
Join the Australian JIA Registry
713 families have registered - help us reach our goal of 1,000 registrations
🔒 Your data is secure and used only for research purposes to improve JIA treatment and outcomes.
Key Initiatives
Our flagship programs making a difference in children's lives
Australian Juvenile Arthritis Registry (AJAR)
AJAR is a national registry of people aged 0-24 years with JIA and related CRDs. 713 children and young adults have now registered in AJAR. We are aiming to reach 1,000 by the end of 2025.
713 / 1,000 registered
IMPACT Study
JAFA's landmark 'IMPACT Study' details the previously hidden physical, mental, emotional and financial burden of juvenile idiopathic arthritis (JIA) and childhood rheumatic diseases on affected 0-25yr olds and their families.
Join Us in Making a Difference
Your support helps fund vital research, provides essential resources to families, and advocates for better healthcare outcomes for children with juvenile arthritis.
Together, we can improve the lives of children with arthritis
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Latest JAFA News & Updates
Stay informed about our latest initiatives and breakthroughs
22 March 2025
A Giant Step Forward
JAFA welcomes the support of frontline peak bodies and allied health organisations in its campaign to reduce delays in the diagnosis...
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15 February 2025
My JIA Booklet in Three New Languages
JAFA is proud to present My JIA, the 'must have' handbook for older children and parents, in three new languages: Mandarin, Vietnamese and Arabic...
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10 January 2025
Early Diagnosis Campaign
JAFA's federally funded, national early diagnosis campaign is in full swing. The campaign is targeting GPs and other frontline health professionals...
Read More →Join Us in Making a Difference
Together, we can improve the lives of children with arthritis