My daughter's disease is ever present in her life, in my life and in our family's life. It guides us daily. It holds her back from things. It holds us back. It makes her think twice before she does what most people do without thinking once! It educates her. She educates me. It makes her very angry sometimes. It makes me very angry always. It makes me feverishly read daily anything I can on Celiacs. But what do we do with this? We live with it. And living with it simply means that we eat differently. Differently than we used to certainly, and differently than most other families. And that is okay. Really. It's still hard but it could be worse. Much worse. We are lucky. Lucky beyond words to have her. Lucky and thankful to have these two lovely, funny, witty and crazy little girls in our lives. So we go forward.
My goal, at least with my current mindset, is to focus on recipes, restaurants (ruthlessly!), current findings, helpful information and of course, sharing still, our story as a family living gluten free out of necessity and not by choice.
I hope you continue to follow us and check back often.
Glad your back. I missed your posts.
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