We are also trying to get out on our own again. There is a really nice place we are looking into. Plus we are still waiting on Janice's chair.
A mother's personal blog starting in January 2012 about daily life and my experiences with my daughter Janice whom was born with spina bifida September 15 2009 and passed away December 26 2012. This is now more about my memories and how I will somehow continue to live on although my child is gone to heaven. I continue to blog about my experiences after loosing her and conceiving her sibling and life as it continues for us.
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Welcome
Welcome to my blog which is about my family and I and how we deal with what life throws at us, which includes my daughter and her disabilities related to her spina bifida and her death on December 26 2012.
Friday, 18 May 2012
Lots on the mind
There is another going on but some of it isn't my place to say anything about. There is some good and some bad, mostly just to much on my mind. Between the happiness at Janice going on the potty to mom's news. Then there was the news from Van (that I talked about last time). My brain feels overloaded.
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