Meet Jo, living with PBC

Jo’s journey to diagnosis began about 10 years ago, when she contacted her GP feeling tired and run down, but it wasn’t until 4 years ago following some routine blood tests and a liver biopsy, that she received a diagnosis. Support groups, like the PBC Foundation, have been a gamechanger for Jo, providing support, education and a like-minded community.

The impact of fatigue: Jo’s Story

Fatigue is more than just tiredness. From her social life to her work life, Jo describes how her fatigue symptoms have impacted both.

Lifestyle adjustments to manage fatigue: Jo’s Story

From diary organization to diet management, Jo explains her individual lifestyle adjustments to manage fatigue.

Knowing liver function: Jo’s Story

PBC affects the bile ducts that run through your liver. Liver blood tests that show high levels of ALP (alkaline phosphatase) are a marker of PBC disease progression. Jo explains why understanding what impacts your liver function is an important part of taking charge of your PBC journey.

Finding a community: Jo’s Story

Jo describes the importance of community in PBC management.

Advice to her past self: Jo’s Story

Jo shares the PBC advice she would give to her past self.

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