Learn more about different roles of patient partners in health research from this insightful session at #PxP25. 👉The recording is available here to watch any time:

What are some unique challenges and opportunities for patient engagement in research in different parts of the world? 👀Watch back this session from day 1 of #PxP25 https://t.co/zZ26hDBPM9

PxP India used storytelling, provocative debate, and Q&A to showcase how patients can convert their lived experience into valuable expertise to help shape research and healthcare processes. Wherever you are based in the world, you can watch it back here:

Looking for a case study on co-design? PxP Australia featured an insightful presentation by @joancarlini and Letisha Living, facilitated by @JanelleBowden. Their #ConsumerInvolvement project used Lego! Intrigued? Watch the session back here: https://t.co/gzqhZZj21p

RT @breastlessAfrik: We did it!!!🥳🎉🙌🏾 #PxP25🇨🇦 has officially ended. Day 3 which was held on the Australian time zone was awesome, fun and…

#PxP25 Truly global. Truly sensitive to different languages (captions), expertise (context/content), and timezones (alarm clocks not always needed). With #AI, we can also ask speakers questions in their local language...not perfect, but progress.

Fellow #Insomniacs Africa🌍 Join us for Day 3 of #PxP25 on the Australian time zone. I am attending from Johannesburg, South Africa. And I am in awe to see my Portuguese speaking #livedexperience/ #patientpartner colleagues from Brazil and Australia participating in the first

'Bold, daring, brave and powerful' 💜 we love that, thank you Ann!

Having a great international chat with patients and researchers at #PxP25. Bold, daring, brave and powerful voices in health research

At the cutting edge: innovations in patient engagement The first sessions of #PxP25 day 3 is underway! Join us now, or consider coming to catch-up at a rewatch party 👉 https://t.co/QS3D4fMtIy #PatientEngagement #ConsumerEngagement #ForPatientsByPatients

If you haven’t yet engaged with #PxP25, it’s not too late. Another great set of sessions for the last day today, live in the Aus Timezone! 👇👇👇

Day 3 of #PxP25 is about to get started. If you haven't joined us yet this year, there is still time to register: https://t.co/lgvHoVWytM Thank you to our wonderful speakers for today 💜 @AggieMN @AhliaGriffiths @JanelleBowden @gillyminn

We can't wait for day 3 of #PxP25! The sessions start at a different time today, to better suit people based in parts of Asia and Oceania. We are looking forward to hearing from today's speakers 👏 If you can't join live - check out the times for the re-watch parties.

@DisabilitywAnna “Academia is not conducive to the kinds of relationships we need to create and the safety we need to create for patient engagement. I have started to build in longer deadlines, especially at the start of the research project.” - Michelle Phoenix #PxP25

@DisabilitywAnna “I’ve learned to not assume what people [patient partners] might be interested in or helping out with. We try to keep the door open in terms of what they would like to contribute to a project.” - Manoj Lalu #PxP25

“As a patient partner, in projects where there have been longer timelines, that has helped a lot. Having a bit more time to meaningfully participate is so helpful.” - Anna Samson #PxP25

“When we shift towards inclusion, we include people’s experiences and improve the research.” - BC Pomeroy #PxP25

“Evidence-based advocacy helps understand patient needs in a systematic manner … and it generally has a greater impact.” “You can point to national and global disparities using evidence-based advocacy.” - Rachel Giles #PxP25

“When we look back at this time, I hope we look back and think about how bizarre it was that patient partners weren’t part of all research.” - Knoll Larkin #PxP25

“Find your own voice and make it as quiet or as loud as you want it to be.” - Rita Schriemer #PxP25