GSD1b Strong Patient Spotlight: Tallulah and Clementine

Being an autosomal recessive disease, parents who carry GSD1b mutations have a 25% of having a child with GSD1b with each pregnancy. This means there are quite a few families in our community with multiple GSD1b children. In this patient spotlight, one such family shares their experience with what they learned with their first child and how that affected the care and management of their second. Clementine and Tallulah’s family also bravely share the impacts that GSD1b have on mental health and remind us that the day-to-day management of this disease are more than just physical. Click through below to hear their story.

Clementine and Tallulah– (Square) by Blair Schneider

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