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Stacy posted this on Facebook last night: “My wish for 2010 is that people will understand that children with disabilities do not have a disease; children with disabilities are not looking for a cure but ACCEPTANCE........93% of people won't copy and paste this, WILL... YOU be one of the 7%…
This is going to be a really short post, but I had to share. I happened to catch Stacy and James napping in our bed. How cute are they? Love these two.
This poor kid (and his parents) just can’t catch a break. Here we go for another hospital stay. But before I get to that, I should probably fill you in with some back story in case you haven’t read the First Trip to the ER post. Even if you did…
James has been having what we think are GI (gastrointestinal) issues for a while now. He doesn’t seem to be tolerating his food well so yesterday we switched his formula from Similac Alimentum to Similac Sensitive to see if that helps. Today we took James to a different GI doctor…
There are so many things going on with James that are beyond our control. There are things about him that we just can’t fix. That doesn’t stop us from trying, though. I don’t know if this is part of the cerebral palsy, or his muscle tone, or a combination of…
As we say goodbye to 2009 and welcome 2010, we wanted to take a moment and reflect back on this past year. What a rollercoaster year it was! Stacy and I spent the first 8 months of the year planning for the arrival of James. After we lost Jackson in…