Welcome to SNAC, our community site that shares information on JIA, events that we hold and much more.
JIA (Juvenile Idiopathic Arthritis) affects about one in every thousand under 16s yet most people don’t even know that kids can get arthritis.
SNAC was set up by parents of kids with JIA to provide support and information for families affected by the condition. On our website you will find information and real life experience about
- The various types of JIA and related conditions.
- The therapies and medicines used to treat the condition
- What is being done to improve the treatments and outcomes
- How to cope, from first diagnosis onwards.
To anyone affected by JIA, we hope you find the content helpful and informative, we have worked with the Scottish Paediatric Rheumatology teams to ensure the content’s accuracy.
Our Heroic Fundraisers
SNAC is run by a group of parent volunteers all of whom have a child with JIA (Juvenile Idiopathic Arthritis) We love what we do and we get enormous satisfaction from seeing the difference that SNAC has made in peoples lives.
NONE of this would be possible without the army of people who give their time to raise funds on our behalf. We’ll ost about as many as we can here but if you have helped and don’t see a post here then please get in touch and tell us all about it – with photos if you can! This is the most recent few, please have a look at the Blogs to see what else has been happening!
The prognosis for JIA has been hugely improved over the last few decades and ongoing research has played a vital part of this. Find out how you can help and why it isn’t as scary as it seems.
JIA is a condition that affects people worldwide as New Zealand Rugby star James Lowe knows only too well. He has been a friend of SNAC for a while now…