Emma joins me from @gingerjello_ for this episode. We discuss how important research and advocacy are and how oftentimes presenting research we’ve done to doctors can be the only way to get answers, of course that brings frustration which Emma also addresses. We also discuss how there is no rule or handbook to chronic illness, and how navigating that can be so incredibly lonely. Validation is such a huge part when living with a chronic illness and it’s so important we find spaces to validate what we’re going through!
