no update

Week 2 and still no update from the Geneticist on Grant and I's blood test.

I received an email from a good friend this week whose son also has developmental delays and I felt like I was reading Adelaide's story. Luckily for my friend they knew their son had a disorder from birth so they were able to start looking into specialist and treatment much earlier on. I tried to give the few words of wisdom that I had, but I know that I was tired of hearing what everyone had to say too.

No two children are the same, but her story was so similar it made me feel like we weren't the only ones out there struggling with this. Maybe it's my ignorance or a lot of my friends ability to hide their struggles, but for the longest time I felt like everyone else I knew had a perfectly healthy child except us. Not that I would change anything, though my arms do get tired of having to carry Adelaide around all of the time.