Kevin’s 4th Birthday
November 7th, 2009 | by Matt |The relentless march of time. That’s how I think of it sometimes. We’re already to what would have been Kevin’s 4th birthday, and I wonder how a year and a half could have gone by so fast. On his last birthday, it was only 6 months after he died and I could imagine him being just a bit older. But now another year later, I find that I can’t really imagine him at age four. I don’t know how he might look different, what he would sound like talking in full sentences, what games he would like to play, and what toys he might be excited to get for his birthday.
Today was a beautiful day outside – temps in the 70’s and perfectly clear. I kept thinking of what a perfect day it would have been for a birthday party. Friends and family would come over, Rich would take some pictures of the kids outside in the leaves, cake, ice cream, etc. I wonder what kind of little boy he would be growing into. Would he still be kind of shy and goofy? Or would he be loud and the life of the party? When he died, life kind of split into "what could have been" and "what is", and his birthday lies on the "what could have been" path. As time goes on, that path grows farther and farther from the one we’re on now, and it’s hard to see it slip away. I find it hard to imagine Kevin at age four. He’s forever age 2 1/2 in my mind, even though life keeps going forward.
Unfortunately, Emily came down with strep throat this morning. So instead of doing something as a family outside in the warm weather, I spent most of the day camped out with her while Dawn took care of Ava to keep her away from her sick sister. Some parents who have lost children choose to do something symbolic on the child’s birthday like letting balloons go or putting flowers at their grave. That is fine, but those kinds of rituals aren’t really what feels right to me and Dawn. We tend to spend the "important" dates quietly remembering Kevin, looking at pictures and watching video. Sometimes it can feel overwhelming to have these dates come, because it feels like there is some expectation of things we should do or how we should feel or what we should say. It’s not always easy to know what to say or do and how much is too much or not enough. We just go with what we feel.
I find it hard that we obviously don’t have any new pictures or video to post and share. I still love Kevin and he’s still my son, and I find that at times I want to share how he affects my life. But I don’t have new pictures from school or him in this year’s Halloween costume. I can’t just say the same things and post the same pictures over and over, even though I want to acknowledge what a day means to me and that he is still special in my life.
We went to a second "grief retreat" a few weeks ago in Iowa City. It was similar to the last one, but we found this one a little easier to get through. There were new people there. People whose child had died since the spring retreat. Everything was fresh and new and raw to them in a way that was so familiar and sad. It was a strange feeling to be one of the parents whose child had died over a year ago. Time keeps marching on.
While we were up there, we also brought all the blankets that our family and friends had generously donated at Ava’s party a couple months ago. We included a note about Kevin’s life and where the blankets came from. They are always so appreciative at the PICU, and the blankets will go to good use. Hopefully some young kid there will have a smile on their face when they get a nice new special blanket.
We also finally did something with all of Kevin’s toys. Over the course of a few weekends, we sorted through them, put all the parts together, and made sure they were clean. We saved some of the toys that held the most memories for us, but really the things he played with most were DVD cases and other odd items. We saved a few toys for Ava, but we donated most of them to the Children’s Therapy Center. They will make use of them in their work or give them to families who can put them to good use. It’s comforting to us to know that his toys are now in the hands of other little boys who can enjoy them, rather than having them sit in tubs in our basement.
We’re fortunate to have family and friends who continue to think of us and remember Kevin, and we appreciate it when you keep us in your thoughts.
7 Responses to “Kevin’s 4th Birthday”
By Jeni on Nov 8, 2009 | Reply
Lily and I just watched Kevin’s 2nd birthday video, and she giggled the whole time. It was like she was seeing the pictures for the first time. We think of him daily, and his smile just can’t be replaced.
By Stephanie on Nov 8, 2009 | Reply
It’s always so nice to come to Kevin’s website and remember him in a special way. I thought of you all so much on Kevin’s birthday and also tried to imagine how that must feel. We also loved the video you put together. What a wonderful tribute to a special little boy!
By Joanna on Nov 16, 2009 | Reply
I always wonder how Kevin would act at four too! I can still hear his giggle, see his smile, and the way he used his hands when he talked sometimes. I miss him more than I can even put in words. I talk about him all the time to Keaton because I never want him to forget “Kiki” his cousin. Thank you for continuing to update his sight!
Love,
Joanna
By Aunt LIZ on Nov 21, 2009 | Reply
I understand the pressure you must be feeling about dates, what to do, how to remember, how to act… But the right way and the best way is what works for you. I would like to offer that I have learned to always rejoyce in the memories and dream the wonder that might have been. There is no perfect recipe to go forward – only perfect memories. Love you!
By Amy Mescher on Nov 24, 2009 | Reply
Hi Matt,Dawn and Family,
I think of Kevin and your family often.Emily and Eva are growing so fast. I wish you also a Happy Thanksgiving. Love, Amy
By Mona Kruse on Nov 24, 2009 | Reply
I find myself thinking a lot about Kevin this week as we begin the holiday season. When I hear Christmas music the tears & memories come, but when I allow myself to feel the hurt I also feel close to him, so it’s not all bad. I miss him so much. Matt, Dawn & Emily, you’re always in our hearts & minds & even more so during the holidays.
By Alberto Restello on Jan 1, 2010 | Reply
Dear Matt, I drop several times on your javascript Toolbox site as I am a programmer and I wanted to tell you what a great job you did but then; once discovered your son story, all the rest became senseless …
I’m the father of 2 wonderful boys (5 and 3,5 years old) and the youngest is suffering from autism.
I cannot say ” I know how you are feeling” but I understand your pain as I’m struggling with all my energies to recover my child.
Even now I can’t stop tearing …
I would only say I feel close to you and your family.
Please accept my best wishes to you for a happy new year.
God bless you all.