Educational Webinar Series

Thank you to all of our wonderful speakers throughout this webinar series.

Without you, none of this would be possible.

The full Webinars with question and answer sessions, extra information, and more resources are posted on the PFIC Network Youtube Channel. Check these short clips out, then head there for a more in depth look at the PFIC disease and treatment.

For instructions on viewing these webinars with subtitles in any language, please see pictures below.

Past Webinars

Medical and Surgical Treatment Options of PFIC

Session 1 Medical and Surgical Options Video Part 1

A brief background about PFIC and the medical management options including nutrition, medications, and medications in clinical trials. Presented by Dr. Jim Squires of Children’s Hospital of Pittsburgh. Question and Answer session at the end moderated by PFIC Network’s Executive Director, Emily Ventura, RN.

Session 1 Medical and Surgical Options Video Part 2

A closer look at current surgical treatment options of PFIC including PEBD, internal diversion and Liver Transplant. Presented by Dr. Kyle Soltys of Children’s Hospital of Pittsburgh. Question and Answer session at the end moderated by PFIC Network’s Executive Director, Emily Ventura, RN.

Session 2 Transplant Life and Complications Video Part 1

A closer look at what to expect when receiving a Liver Transplant, and how life changes after. Presented by Dr. Jim Squires of Children’s Hospital of Pittsburgh. Question and Answer session at the end moderated by PFIC Network’s Executive Director, Emily Ventura, RN.

Session 2, PFIC Specific Complications of Transplant

Diving deep into unique aspects of PFIC, this webinar focuses on some of the considerations that PFIC 1 & 2 patients may experience post transplant. Presented by Dr. Kyle Soltys of Children’s Hospital of Pittsburgh. Question and Answer session at the end moderated by PFIC Network’s Executive Director, Emily Ventura, RN.

Genetics of PFIC and it’s subtypes

Join the PFIC Network and our host, Richard Thompson, Professor of Molecular Hepatology at the Institute for Liver Studies, Kings College London and Consultant Paediatric Hepatologist, at King’s College Hospital. He will discuss the seemingly complex topic of the Genetics of PFIC including the various subtypes and why they are each so unique. He will dive into some of the barriers behind genetic testing and why PFIC is so difficult to treat. He will also give us a quick look at what has been recently discovered in the genetics of PFIC. Moderated by PFIC Network’s Executive Director, Emily Ventura, RN.

Mental Health: Coping Strategies for the PFIC Patient and Caregiver (Full Length Video Coming Soon)

From a fairytale family to losing three brothers, maternal advocate Cristol Barrett O’Loughlin draws on personal tragedy to ease the suffering hearts of others. Her inspiring stories of courageous #RareMothers, reveal the secrets to sustainable self-care and wellness. Forget “PTSD” — more accurate is “CTSD” (Chronic Traumatic Stress) — as our rare community grapples with the realities of long-term caregiving and disease management. There is a purpose to our pain. With guided meditations and her signature infectious enthusiasm, Cristol gently nudges us all to move beyond “Why me?” into “What can I do to help others and to help myself? Moderated by PFIC Network’s President, Melanie Karakaidos.

Upcoming Webinars

PFIC 101

Children’s Hospital Colorado will host the webinar and provide an overview of PFIC for patients and families. They will go over what to expect throughout the journey of PFIC- from a new diagnosis, to exploring treatment and management options including nutrition management, medication/ surgical management, and clinical trial considerations, all the way through to when/if to expect the discussion of liver transplant. December 8, 7:30-9:00 pm EST (USA)