We know that living with an autoimmune condition is often complex, unpredictable, and exhausting.

Many of us are managing our symptoms while maintaining work and home commitments, often squeezing in time for medical appointments. We’re juggling parenting with getting enough sleep, eating well, staying on top of housework, shopping for groceries, and maintaining relationships – while tracking our symptoms, flare triggers, and how our bodies respond to treatment.

By the time we finally make it to a doctor’s appointment – where we need to convey this information accurately and efficiently, usually in a short space of time – we can feel like we’ve let ourselves down. Too many of us leave thinking, ‘I forgot to mention that,’ or ‘I didn’t explain it properly.’ This is especially common if we’re exhausted or feeling unwell, as it can affect how we process information, and communicate. We know how important it is for your doctor to listen and respond to our feedback so we get value from each appointment, and our treatment reflects your true experience. We feel your frustration and you’re not alone, and that’s why we’ve created these tools. Our tools are practical and easy to use, to encourage easier communication with your doctor.

Use our tools to track your symptoms, test results, pain levels, and day-to-day impacts, so you can arrive at appointments feeling more prepared and confident.

They are designed to support meaningful collaboration with your doctor and are not medical advice, but simply a way for you to take a more informed approach when talking about the your treatment plan. Most importantly, these tools are shaped by you. They’ve been developed by listening to our community in our Dragon Talks sessions, learning from shared experiences, and partnering with other organisations where needed. Your voices, challenges, and ideas guide what we create. As our community grows, so will our resources – always grounded in real needs, real lives, and real support. We hope you find these tools helpful on your journey, and we always welcome any feedback.

MPaCT

Living with chronic pain is exhausting. MPaCT helps you express not just where it hurts, but how it’s affecting your everyday life. It makes sure your healthcare team is getting the full picture.

Do you want to join our Newsletter list to hear about our News, Events, free Expert Talks and more?

My Numbers Tool

Use this tool to track your tests results and symptoms to help reveal any patterns, which can be useful to advocate for any changes to your treatment plan. This tool was designed to make communication easier with your doctor by showing you have tracked your symptoms and recorded your test results. My Numbers Tool is proudly endorsed by the Australian Rheumatology Association (ARA).

Do you want to join our Newsletter list to hear about our News, Events, free Expert Talks and more?

icon

Autoimmune Conditions and the importance to Know Your Numbers

Dragon Claw’s own Dr Charmaine Jones was the driving force behind the need for a tool for people living with autoimmune conditions – a tool to their own symptoms and test results to empower them to be a more active participant in their treatment plan. Being able to show your medical practitioner a picture over time, to be able to better advocate for themselves. In this episode, rheumatologist Dr Daniel Lewis talks to us about the benefits of using a tool like this to help identify if medication is working for you, or if you need an adjustment.
icon

MyFlareUp launches new pain communication tool (MPaCT) at Parliament House

MyFlareUp was honoured to launch My Pain Assessment Communication Tool (MPaCT) in partnership with Painaustralia at the Parliamentary Friends of Pain Management event on 10 March 2026 at Parliament House in Canberra, Australia. This event brought together patient leaders, clinicians, advocates and policymakers to discuss the future of pain communication in Australia – and the urgent need for reform.
icon

How does My Numbers Tool work?

After MyFlareUp's research project with Community and Patient Preference Research (CaPPRe) in 2024 found some alarming stats, we needed to explore why so many people in the autoimmune community today still continued to have severe symptoms, despite there being new treatment options available. We discovered that of the participants surveyed, 45% of them knew nothing about biologics and 56% of them knew nothing about JAKi’s, and 34% of participants were on the same medications and dosages over the past year, despite them reporting moderate to high disease burden. We also found that 52% of participants believed there were no further treatment options available to them, other than what they'd used before.