Yesterday I read this article published by The Age newspaper based in Melbourne, Australia.
It got me thinking.
Last year, when R was recently diagnosed, I struggled with the question, "Does this mean I have a special needs child?"
I was also asked that of several well-meaning people, although at the time it was hard to answer. Because R seemed so normal aside from his speech delay, it was really hard to come to terms with whether or not he was a special needs kid.
Admittedly, I as a parent would not have actively chosen to have a kid who has special needs. I realized that while I am taking this journey with R. But for reasons I have yet to fully understand, God has blessed us with this little boy, SPD and all.
And by His grace, I know that there are others in worse situations than us.
I am in several Facebook groups. In one of them, I read of a little guy named Caleb Munn. As of this posting he is eight months old, and is recovering from a liver transplant.
Yes you read that right.
Caleb was diagnosed at two months old with a severe liver disease called Biliary Atresia.