Fighting a rare disease can be lonely. Whether you are a parent looking to join the fight against SJIA or a researcher interested in SJIA, join us.
If you are a patient, you will be added to our patient database, you will receive our newsletters with helpful primers and summaries of the latest research. You will also find out about clinical trials and research studies you might be eligible for.
If you are a researcher, you will find out about funding opportunities. You will also receive periodic updates about our patient database which might help you plan your research.
We will never share your email address with anyone.