My new blog where I will attempt to post about my new life as a Chiari wife and the mom of 2 beautiful big girls and one "tiny" baby girl. Join my on my journey to self discovery, as I attempt to cope with the life God has given me.My husband has a disease called Chiari Malformation. He was diagnosed on June 23, 2008. On July 3 we pre-registered him at the hospital, and on July 8, 2008 my husband had brain surgery. My whole world felt like it was crashing down around me. He is doing okay right now (6 months later), but our lives are changed forever and I have a hard time dealing with that. He will live with this the rest of his life and there is not a cure. Our faith in God has not wavered. We put our worry HIS hands and I am confident that things will turn out OK. We are blessed to have had the last 6 months to be a family. We don't know how long my husband has, but we are most definitely going to make the most of it.
This blog is basically my place to vent.....worries, feelings, thoughts, anything I feel like writing. I don't know that anyone will ever read it (besides me) but that's not why I'm writing it anyway. It's just nice not to have to keep it all bottled up anymore.












Wow, I'm so gald you joined blogworld. i think you will find a stream of comfort and support here. I'm sorry to hear about your husbands disease. I would like to know more about it. What does this disease do? Hugs!
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