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Introduction

This blog is intended to provide information and updates on Beckett’s (and our) journey with hypoxic ischemic encephalopathy (HIE), Cerebral Palsy (CP) and Curririno’s Syndrome and how we are doing as a family of three. More than that, it is a way for us, Beckett’s parents, to share and process what we’ve been through as a family. Honest feelings and emotions will be shared. We think and hope that it will be therapeutic in some ways for us, and perhaps for others.

Originally, we wanted to start a blog as a way to keep family and close friends up to date, but have decided to allow the site to be public. Maybe it will bring someone going through a similar situation some comfort in the future. Feel free to share the site or my contact info with others you may know going through something similar, if it might bring them comfort.

I guess it's probably also worth noting that we often call Beckett "Little Bee", hence the name of the blog! 

This blog is written by Mom (Chantale). It is edited and reviewed by Dad (Keith) and Melanie (a.k.a. Aunty Mommy). 




Disclaimer: 

1. This blog is not intended to provide any medical information, recommendations, advice, or diagnoses. Any medical information described is based on our best recollection and understanding as non-medical people…

2. At no point in this blog is my intent to hurt anyone’s feelings or make people feel guilty or bad about things done or said. I’ve written a true reflection of my feelings through this process, but I know our friends and family have always had our best interest at heart.

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