This #JIAAwarenessWeek we wanted to share some of the tips for talking to friends about JIA from our brilliant JIA magazine, made by young people from one of our art therapy groups who live with JIA! 🫖 You can download and print the full magazine here: ow.ly/1Rm650SwZJp

🌟 It's Day 4, Meet Megan! 🌟 She's 18 and has been a warrior against polyarticular #JIA since her diagnosis at 20 months old. 💪 Despite the challenges of having 33 joints affected, Megan shines bright as an advocate for inclusivity in the performing arts industry. 🎭✨

Check out our BRAND NEW Taylor Swift inspired t-shirt. Fans of the Eras Tour will recognise the iconic white #swiftie t-shirt with black and red font. We've created our own version to help raise awareness that #ChildrenGetArthritisToo

Day 5 of #JIA Awareness Week! 🌟 Meet Clare, the incredible Mum to 10-year-old Zak, who was diagnosed with JIA at just 4. 💪 Despite the challenges of JIA spreading from his knees to his hips and dealing with uveitis, Zak is a warrior! 💙

For JIA Awareness Week 2024 we wanted to reshare this blog written by the brilliant Kayleigh about her experience living with JIA, art therapy with Teapot Trust, and the community it brought her. Art work by Kayleigh, and you can read the full blog here: teapot-trust.org/blog/kayleighs…

Amazing work for all those involved! Thank you for your fantastic work on raising awareness and vital funds for JIA 🥹💜

Here’s a look back at JIA Awareness Week 2024! 🎥🌟 Thank you to everyone for joining us in raising awareness, sharing their stories, and supporting the JIA community. Together, we’re making a difference, one step at a time. 💪💜 #ThisIsJIA #JIAAW24

We are very grateful to FDC Law Solicitors for choosing NRAS as their Charity of the Year. For #WearPurpleForJIA in May, they really pulled out all the stops – wearing purple and raising funds and awareness of our families living with juvenile idiopathic arthritis (JIA).

Have you got questions about life with JIA? 🤔 Drop them in the comments below! 💬⬇️ We're here to provide answers, share tips, and support you on your journey. Let's tackle JIA together! 💪 #JuvenileRheumatoidArthritis #NRAS #JIACommunity #AskNRAS

Maddy Roberts, our Families and Young People's Services Manager has arrived at #PReS2024. We are excited to be attending talks from many healthcare professionals and researchers from across the EU - beginning the day with a Global MSK health working party 🔬

Next up … JIA Working Party Meeting taking place at #PReS2024

📢 If you are a Healthcare Professional and have experience with RA or JIA, please take a moment to help NRAS to deliver the support needed for the healthcare sector and patients by completing our survey. Sharing your thoughts will help guide us into improving, refining, or even

Attending a Grand Debate this morning at #PReS2024 - Step Up vs Step Down Therapy in non-systemic JIA 📝

CCAA and many of the families we support have been involved in the fantastic The IMPACT Study from the start. Great to see it being presented at #PReS2024

An insightful morning at #PReS2024 listening to talks around patient pathways, patient involvement and a grand debate exploring Biologics vs Biosimilars 🇸🇪

A fantastic presentation updating on the progress of the The IMPACT Study from Dr Polly Livermore and Klaudia at #PReS2024. The work you are doing is absolutely invaluable to patients and families living with rheumatic conditions. We can’t wait to see the outcome of the next