
Good Evening!
We are sitting here, listening to the Republican National Convention. I don't dabble in politics often (Brandon does that enough for both of us), but it is interesting to hear the perspectives of those that are speaking. I am excited about a woman running on the McCain ticket. I look forward to hearing her speak tonight.
This week has been a good one. Brandon and I took a trip to Chicago over Labor Day weekend. The time without the kids was so nice. It was great for us to be able to rest, relax, shop, and eat on our own schedule. We took in some of the sights of the city, slept in, and ate ourselves into oblivion. The kids spent time with Grandpa and Grandma McKinney in Baldwin, and, despite spending three days there, Kylee still cried when it was time for her to come home with us. They had a blast over the weekend, too.
Friday was a difficult day as we learned that baby Gabriella Duffet, at 55 days old, passed away. We have come to know Gabriella's family through Alexandra's House. Gabriella was born on July 5th and had Trisomy 18. As I mentioned in a previous post, she defied the odds by being here on earth with us for as long as she was. As her Daddy said on their family blog...Gabriella sprouted her wings and went to heaven....on August 29th. It brought back many painful memories of losing Caden, and, again, the question "Why must anyone endure this kind of pain?" We may never know. Of course, our love, thoughts, and prayers continue to be with the Duffett family. Please include them in your prayers as well.
Saturday was the two month anniversary of Caden's birth. I felt funny and then realized what day it was. I often find that my heart tells me when an anniversary date is approaching even if I don't consciously realize what the date is. I was grateful that we were doing something fun together. It made the day more bearable.
I am finding more peace as the days go by. There isn't a day that I don't miss our baby, but time is healing our wounds. Life is moving forward. Brandon and I talk about Caden often. The kids are doing well...Kylee hasn't had any more meltdowns, although she still looks at the baby stuff in Target with sad eyes. Above, you see her wearing her napkin on her head at dinner. Look out, Little Red Riding Hood!
We are picking up the pieces and finding our new normal. I have found that I speak of Caden in normal conversation as one of our children, which, of course, he is. Sometimes it catches people off guard, but it feels good to say his name. Some inquire about him when I mention his name, and it gets easier to share his story each time we do it. As we share our story, we have found that many people open up and share their own story of loss. It is humbling and soothing all at once. Many have looked at Caden's picture in our entryway and commented on how beautiful he was. We agree. :)
On Saturday, our friends will be here planting flowers and shrubs in Caden's garden. We are excited to see it all come together. We will dedicate the garden in just two weeks...another step in the healing process for us. We will post pictures when it is finished.
We are so grateful to have a garden full of living, beautiful things to help us memorialize our baby boy. Thank you so much to all of you who have helped bring the garden into being.
We continue to appreciate your love, thoughts, and prayers. Keep them coming!