Isla’s mum opens up about receiving Isla’s PKU diagnosis and navigating the early stages of being on a low-protein diet, especially during weaning and toddlerhood. She shares how they’ve adapted to the low-protein diet while allowing Isla to grow, play, and thrive like any other child. This heartfelt story reminds us that a diagnosis doesn’t define a child—it’s just one part of their journey.

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This article does not consitute medical advice or professional services. Consult your doctor and dietitian before making any changes to your diet or protein intake to ensure the right nutrition to support your unique needs.

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