A diagnosis can derail your life, your career, and your confidence in your own body—but it doesn't have to define your future. Julie Croner shares her journey from childhood joint problems and years of uncertainty to a life-changing psoriatic arthritis diagnosis in her 20s. Along the way, she faced avascular necrosis, complex regional pain syndrome (CRPS), melanoma, chronic pain, and a period of disability that left her struggling with her independence and identity. Julie explains how tracking her symptoms like a data analyst helped her identify personal triggers, advocate for herself with doctors, and reclaim a sense of control over her health. With the help of her mom's legendary medical binder and an online community, she went from feeling alone to building a career centered on patient advocacy. We also get honest about the challenges of living with autoimmune disease while navigating relationships, fertility concerns, pregnancy on biologics, breastfeeding, and raising four children. Julie shares the fears she faced about passing autoimmune disease to her kids, how she navigated her youngest daughter's life-threatening medical crisis, and why flares can sometimes arrive after the storm has passed. This conversation is a reminder that bad days don't equal a bad life—and that a diagnosis doesn't erase your worth or your ability to build a meaningful future. In this episode, you'll discover:How Julie's childhood symptoms and knee surgeries eventually led to a psoriatic arthritis diagnosisWhy her mom's medical binder helped connect the dotsHow an online autoimmune community changed her sense of isolationWhat six months of tracking food, sleep, pain, activity, and other symptoms taught herHow she used data to have more productive conversations with her doctorsWhat it's like to navigate fertility, pregnancy, biologics, and motherhood with autoimmune diseaseHow Julie turned her lived experience into a career in patient advocacyJulie works with Health Union and the Social Health Network, helping connect patient leaders, caregivers, and healthcare communities and amplify patient stories. Whether you're newly diagnosed, struggling with chronic illness, considering pregnancy, or learning to advocate for yourself, this episode offers practical insights, honest conversations, and hope for the road ahead. Timestamps00:00 – Introducing Julie's autoimmune journey 00:52 – Childhood symptoms, knee surgeries, and psoriatic arthritis 01:44 – Severe illness, chronic pain, and losing independence 02:39 – The “mom binder” that helped connect the dots 05:32 – Avascular necrosis, CRPS, melanoma, and treatment challenges 06:57 – Finding community through SpoonyChat 07:55 – Six months of symptom tracking and identifying triggers 08:50 – Using personal data to advocate with doctors 09:46 – Turning lived experience into patient advocacy 11:30 – Health Union and the Social Health Network 16:56 – Dating, relationships, and fears about being lovable 23:00 – Pregnancy, biologics, and breastfeeding 27:24 – Managing autoimmune flares while raising four children 29:02 – Her youngest daughter's medical crisis and delayed flares 34:15 – Fear of passing autoimmune disease to children 36:01 – Food, inflammation, and identifying personal triggers 39:40 – Advice for women with autoimmune disease who want a family 40:57 – Strength, faith, and accepting what you cannot control 42:43 – Why sharing your patient story matters 45:07 – Where to find Julie Connect with Julie: Learn more about her patient advocacy work through Health Union and the Social Health Network. https://www.instagram.com/itsjustabaddaynotlife/