This is the second post in a 2-part series reflecting one year after we found out our son would have Down syndrome. You can find Part 1 here. Following our diagnosis, we had limitless support from our family, friends, doctors, and our local DS organization. But we still didn’t have our baby in our arms yet. There was so much we didn’t know about him and all we had were statistics and other people’s stories to try to piece together an image of what our lives would look like. Stats and probabilities weren’t really doing a great job painting a picture of the future. Here are some of the things our doctor wasn’t able to tell us about our son that day. Continue reading
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