Noah's Book

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Myths about Hydranencephaly

Dear Doctor Letter

Here is a book that Lisa made for her son Noah when he started school in the spring of 2005. Some of it is appropriate for the children and other parts of it are more appropriate for those caring for Noah. It can also be used as part of a care plan as discussed in Chapter 13

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There are more pictures and pages to Noah’s book that are not shown here.

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August 16, 2001- January 12, 2005

This website is funded in loving memory of Jason S. by his mother Kammy

The information on this site is provided by families, caregivers, and professionals who are or have been caring for a child with Hydranencephaly.

Please report any broken links or missing photos to angelbearmom@shaw.ca