Since becoming a mother I have found that I have done a lot of grieving. I grieved for all the things that Janice wouldn't be able to do because of her spina bifida. I grieved the fact that Janice had spina bifida. Then when I thought I was done grieving and had come to terms with what Janice's life was meant to be and was finding joy in the things that she found happiness in, then we lost her. I then began grieving the loss of my daughter Janice. I still don't understand why we had to loose her. Now I find that I am again grieving. This time I am grieving the relationship that my daughters will never get to have. The sisterly bond and connection that all sisters should share that my daughters will not get to experience.
So much grieving in such a short time. It isn't fair.
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 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.
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