It’s hard to believe that a whole year has passed since we launched Project IMPACT. The time has flown...
The 2024 PFIC Family & Scientific Conference in April was our largest conference yet! We had 138 in person...
By: Lisa Jensen, PFIC Network Support Group Facilitator When one family member receives a diagnosis of a rare disease...
Our time at the 2024 ESPGHAN conference was incredibly productive and motivating! The ESPGHAN Congress is an annual meeting...
Did you know that there are several research networks dedicated to studying PFIC and other rare liver diseases? Sometimes...
