Empathy is a sweet and beautiful thing. I think our experiences with Silas's delays have given us a taste (albeit a small one) of what it feels like to have a "special" child. Our membership in this club is not a full one. Maybe it could be called "honorary," and we hope it will be temporary.
I wept today as I read this story about the birth of a Down's baby. Wow, she is a gifted writer.
The pain that one feels upon realizing that (or in our case, wondering if) your child will be different for the rest of his/her life, will be labeled by others, will struggle, will suffer...is unimaginable.
I think that before we went through these emotions with Silas (about 8 months ago now), I had just thought of parents with special needs kids as just that--parents of special needs kids. As if that's the way they always were, as if it seemed normal to them. I admired them, but I never thought about the pain they must have felt When They Found Out. No one plans to have a special needs kid. When imagining and daydreaming about your future family, you just don't THINK of that possibility.
I am thankful for the hope that we have in the Lord. His plan is perfect. He makes no mistakes. His sovereignty extends to even the most painful circumstances.
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i love kelly hampton. i follow her blog religously. she is so inspiring. and nella is an angel.
ReplyDeleteThanks for the link. So encouraging and honest.
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