Great to hear that a group of experts were together to help the Still's and SJIA Community. #curesjia SJIA Foundation

Wow! WordDay 2023! A lot of events around the world will continue to bring awareness to pediatric rheumatic diseases. And first time in Brazil! Can't believe I am part of this journey... very grateful! #curesjia SJIA Foundation Claudia Saad Magalhaes MD @canchild_ca Filipa Oliveira Ramos

Yesterday, Bia and I were part of WordDay UK! 🥰 #curesjia

Post will be in Portuguese, working in translation to English... #WordDay2023 emocionante aqui no Brasil! Pais, pacientes e medicos juntos, em prol de tratamento eficaz para os pacientes. Dr. Olaf (Dr. Olaf) fez um resumo excelente. Obrigada a todos! devpeds.medium.com/wordday2023-br…

Fantastic talk this morning at #CARRA2023 I professionally work in a different field (though it overlaps with health) but this discussion on Racism is so relevant & I will be discussing w/ my team to reassess some guidelines and expectations in our community work Dr. Tiffani Johnson, MD, MSc

Excellent thread about IL-18 levels and SJIA in @CARRA Annual Scientific Meeting. Full article below. #curesjia academic.oup.com/rheumatology/a…

Another impactful slide from #carra2023.

Thank you Komodo Health Team for inviting the SJIA Foundation to this Panel. It is always great to share our thoughts and raise awareness for SJIA patients #cureSJIA

Simple article: One same disease, diverse phenotypes, multiple challenges #curesjia jircohorte.org/post/systemic-…

Our community is heart broken today… 💔 Hope the cure is not far. #curesjia

Always great to remember and see the backstage of a great panel. #curesjia

Feelin very proud and emotional…. After difficult SJIA days (and seams like a decade ago), my daughter is again taking something great out of SJIA. Way to go Bia! I am sure you will rock! Thank you SJIA Foundation for all the support always! World Orphan Drug Congress USA

WODC 2023 is over. Still proud and delighted with the work of these young people. And other people noted their hard work too. Here is the post from Julianne Mills, Rare as One CZI, on LinkedIn. CZI Science SJIA Foundation World Orphan Drug Congress USA #cureSJIA

Just starting! #PReS2023, so great to finally meet in person a lot of familiar faces. Pediatric Rheumatology is a very special community. SJIA Foundation connecting the dots in Europe! 🇪🇺🇳🇱

Just starting! Already met some familiar faces but missing my friends from SJIA Foundation Foundation. Great to be here once more. #PRES2024 #cureSJIA

For SJIA/Still’s patients, rare disease day event organized by Systemic JIA Foundation.