My son, Liam Purser, was born on Dec. 16, 2011 with a condition called Semi-Lobar Holoprosencephaly (HPE). When we first heard this word I was overcome with emotion because for one I couldn't even pronounce it, let alone comprehend what it was. Since that time we have learned much about this condition but the ultimate thing we have learned is that the Dr's can not tell us what to expect of our son. Every case is so unique and so our Liam will have his own unique journey and so far that has been true.
With any condition that deals with the brain there are many "unknowns" and the expenses accumulated to help us care the best for our little fighter are, and will be, anything but small. Anything that you are able to contribute to help us will ultimately allow us to give Liam the best life a child with his condition can have. And with that it will allow Mom & Dad to get the necessary things we need to help care for him. I hope you will read this blog and become a friend of Liam's and embark on his journey with us :)
Thank you for Visiting
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