So it’s only day one of 2014 and I am already behind. First, I never finished getting my Christmas cards out so if you didn’t get one enjoy this digital version, because I’m not going to even try. Second, my birthday. I am probably the only person in the history of Facebook who didn’t thank everyoneContinue reading “Slowing down”
Tag Archives: our story
Lost in the little things
We don’t talk much about Reese’s development. In many ways it’s her biggest problem from all that we deal with every day. Of course she doesn’t know it, well most of the time. Sometimes she looks at me and is so intently talking to me with her eyes, I feel like she must be frustratedContinue reading “Lost in the little things”
A kiss to build a dream on
First, I want to make sure anyone who is following our story and/or is new to epilepsy knows something. Millions of people live with this disease. Most likely Reese isn’t the first person you’ve come across. You just didn’t know it. Thousands and thousands of people live with this disease and find ways to manageContinue reading “A kiss to build a dream on”
My favorite pictures of our family of all time. (so far). Back in April in the bluebonnets. Love seeing Reese’s smile and how much Davis loves to love on her.
All is quiet…
If you haven’t figured it out yet, we go dark when things are good. Davis starting school has been so fun for us and overall the summer was good. We are so happy with all of Reese’s progress and we share all the big and little moments with photos and video… I predict a firstContinue reading “All is quiet…”
Why I love 3D now, the trip update
We know everyone is on the edge of their seats waiting for the big update. We don’t label this as good news exactly, but we do feel we have new insight thanks to some creative investigating by the specialist at Lurie Children’s. Seems we may have found physical proof of the culprit causing Reese’s seizures.Continue reading “Why I love 3D now, the trip update”
OK With Change 