Living My Best Liver Life with Livie Wells

Season one, episode three, features Danielle a Respiratory Therapist and PBC patient who shares her diagnosis journey, challenges, managing multiple autoimmune conditions, (including Sjogrens and MCAS), the impact of working through COVID pandemic she discusses treatment, symptoms, management and lifestyle adjustments and the emotional effects of chronic illness. Danielle also highlights her advocacy work as president of Friends of the PBC Foundation - in the US, the importance of patient communities and practical strategies for navigating care and preserving mental health while living with PBC. *I would like to make a correction, please note that Danielle has one very sweet, smart and talented cat named Juniper Peaches.  YES,  I did say that Juniper Peaches plays video games! 

In this episode of Living My Best Liver Life, host and guest Jackie discuss her diagnosis with primary biliary cholangitis (PBC), the long road to correct diagnosis, and the added challenge of fibromyalgia. Jackie shares how she manages fatigue, treatment struggles, lifestyle changes, and caring for her family— including her daughter’s recent health issues and gluten sensitivity. The conversation focuses on resilience, practical strategies, and the importance of support and self-compassion.   I am not a medical doctor. My guest is not a medical doctor. We are sharing our stories, experiences and advice. Please seek medical advice, testing and treatments from your medical doctor or specialist. If you are experiencing a medical emergency please dial 911 on your phone. 
If you are experiencing a mental health emergency please dial 988 on your phone. You can also text HOME to 741741 for the crisis text line in the US which is a free confidential service. 

 Please know you are loved,  you are not alone,  and I am here with you. 
Xo Livie   

I’m excited and a little nervous to share this episode one of “Living My Best Liver Life”. In this first episode, I share the story behind the podcast, my journey through chronic illness and liver disease. I also share why advocacy matters so much to me. My hope is that this podcast becomes a supportive space for patients, caregivers,  advocates, anyone looking for encouragement. I’d love for you to listen, subscribe and send me your “Itch or Bliss” for future episodes. What’s a “Itch or Bliss” you say? Tune in now and you’ll find out!