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Avatar of Elyse

I am from Ontario, Canada. Recently my premature son was found to have PKU, he is now 17 days old. It was a struggle to deal with at first to know that worst case senario, my son could not eat very much of our everyday food. Due to lots of research on the topic and helpful posts from people, we have found that it is an obstacle but not impossible. This website is just fantastic, and wonderful. It has eased my mind tremendously to know that there is support and others going through the same stress.

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