Click to download pdf booklet
My JIA is an information booklet for children and young people, parents, carers and schools about managing life with Juvenile Idiopathic Arthritis (JIA).
Being diagnosed with JIA can be scary and daunting. You might not have even heard of the condition before. But you are not alone. JAFA is here to support you on your JIA journey.
This booklet will give you an outline of your condition and what to expect. It is written for ‘you’ – a child or young person with JIA. Your parents, carers, family and school will also need to read it. Electronic copies are available on our website to share with them.
Remember that your doctor, nurses and whole healthcare team are the experts. Ask them for specific advice when it comes to your treatment and medications, or if you need some support. When looking for more information, be careful what you read and who you listen to, including social media. Look for trusted sources, such as our website www.jafa.org.au especially the videos on talks by leading Australian paediatric rheumatologists at: www.jafa.org.au/jafa-symposia-series
Above all, remember that you are not alone. Your paediatric rheumatology team and JAFA are here to support you.
