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What if you had the power to navigate your own health decisions, armed with accurate information and backed by a supportive community? In this fascinating episode, we share our journey of advocacy for endometriosis, protecting the community by ensuring they receive correct and helpful information. We recognize the value of personal recommendations in selecting healthcare providers and stress the significance of mindful advocacy. With an eye on the future, we touch on the series coming up in 2024 covering topics such as interstitial cystitis.

Having diverse voices in the podcast space is not just an ideal, but a necessity. Especially when discussing a complex issue like endometriosis, experiences can differ vastly based on our backgrounds. In our conversation, we underscore the importance of bringing the unique experiences into the spotlight. We also examine the different challenges of navigating endometriosis in different countries and the critical role of evidence-based research. At the same time, we open up about our lessons learned as podcasters, the surprises we've encountered, and the overwhelming support from practitioners in the endometriosis community.

As we wrap up this illuminating discussion, we delve into the future plans and priorities for our podcast. We emphasize the importance of addressing co-conditions alongside Endometriosis, as well as the power of diverse voices from different countries and languages. As well as fostering an intentional space to support couples of all backgrounds. Finally, we express our heartfelt gratitude to all those who have supported our podcasting journey, reflecting on the importance of community when dealing with chronic illnesses and the lessons learned thus far. Join us and be a part of this journey as we advance understanding, advocacy, and empowerment in the world of endometriosis.

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https://insixteenyears.com/
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Kathleen King- DEARG

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