connecting the dots to find a cure for Systemic Juvenile Idiopathic Arthritis

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:supportGroupHeader-02Fighting 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.

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Systemic JIA Foundation

3 weeks ago

Systemic JIA Foundation
twitter.com/sjiafoundation/status/1630655502970396675 ... See MoreSee Less

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Systemic JIA Foundation

3 weeks ago

Systemic JIA Foundation
Today is #RareDiseaseDay - how are we at Cassie + Friends creating a space for our community (you) to learn, raise awareness and add your voice to the conversation? We'll be marking it with our RareTalks: Genetics and Childhood Rheumatic Disease session! An opportunity for everyone in our community - families navigating #JA, #TRAPS, #Lupus, #FeverSyndromes, #JDM, #DADA2, #Undiagnosed, #CRMO, #Vasculitis, #SJIA and all other childhood rheumatic diseases - to come together to learn about the role of genetics, ask questions, and connect with other families in our breakout room chats. This is the biggest and first virtual and national gathering of autoimmune autoinflammatory and undifferentiated/undiagnosed families from right across Canada.Not just today, but every day, we work with our community of healthcare, parents/caregivers, youth and patients, community partners and beyond to grow this community, get even more people involved in our mission, and raise awareness for further support, education, research and connection opportunities with the hopes that one day, we'll be meeting you all in person to mark #RareDiseaseDay together. Until then, we hope to see you all online tonight. If you haven't registered yet, it's not too late! Head over to cassieandfriends.ca/event/raretalks-genetics/ to RSVP.----#RareDiseaseDay #rarediseaseday2023 #juvenilearthritis #lupus #autoinflammatorydisease Autoinflammatory Alliance Canadian Arthritis Patient Alliance Arthritis Society Canada Jarproject Arthritis Broadcast Network The Flying Lifeguards Arthritis Research Canada Canadian Pain Society CRMO Foundation Systemic JIA Foundation Arthritis Foundation ✌ ... See MoreSee Less

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Systemic JIA Foundation

1 month ago

Systemic JIA Foundation
For Rare Disease Day this year, the SJIA Foundation is organizing a social hour. Bring a cup of tea / coffee (or your favorite beverage) and join us! On Saturday, 25th Feb, at 10am EST | 3pm UTCPlease register here: tinyurl.com/sjia-aosd ... See MoreSee Less

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Location 3584 Outlook Avenue, Cincinnati OH, 45208

Email Address info@systemicjia.org

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Disclaimer

This website is provided for educational and informational purposes only. Systemic JIA Foundation is not engaged in rendering medical advice or professional services and this information should not be used for diagnosing or treating a health problem. The site authors and the content providers make no representation or warranties, expressed or implied. Providing links to other websites does not imply that Systemic JIA Foundation endorses the information or services provided on those websites. The organizations operating those websites are solely responsible for the content found on their websites.