So everything is over. The funeral was absolutely beautiful and I plan to write an entire blog post about it–with pictures and a copy of the talk I gave–for those that want it. We are home now and everything feels weird. It somewhat feels like everything I have been experiencing over the last 5 months or so were leading up to his funeral–and now I don’t know what to do or how to feel. For the most part I feel normal and a bit like I just had a bad dream. Because I never really had Isaac in my life, I feel like his presence was almost phantom like.
Until I think of our family. It doesn’t feel complete without him. Aaron and I were asked how many children we had the other day by an old acquaintance–they knew about Isaac, but hadn’t made the connection between the story they had heard and meeting us again in person. When he asked us, Aaron and I froze and looked to one another for an answer. Neither of us spoke and both kind of let out an awkward chuckle–not really knowing how to respond–so we stood there stammering. In an attempt, I’m sure, to understand the awkwardness, this man shuffled through information in his memory and remembered our situation. He felt instantly remorseful for his question. You could physically see when he realized what had just happened. It wasn’t his fault. Really, there is just no way to always be careful and considerate in a situation like that. He hadn’t see Aaron in years–had heard our story through someone else, so I felt bad at his embarrassment. There was nothing we could say that would make him feel better though. It was hard and awkward for all of us.
Ironically, we ran into another of Aaron’s friends that night–but this man had lost a child in December. His wife was 8 months pregnant. Sound familiar? Their situation was completely different than ours, but the outcome was the same and we could understand and relate with each others grief.
How opposite those two encounters were.
What was interesting about the second one was talking to a fellow parent who had lost their baby. It would seem they knew exactly what we were going through–and we them. But in reality neither of us could understand. Our situations were so different. I had a hard time with that over that past few weeks, when message after message came flooding in of people telling me their stories. While I sincerely appreciated their vulnerability and putting themselves out there, it was hard for me not to want to say “you have no idea”.
Sometimes, in our hurt and grief, we feel as if we are the only ones experiencing pain. It’s hard to relate with others when they aren’t experiencing what we are–even if it’s similar. I hated every time someone told me that they had also lost a child. It seemed to make my anger grow. Why could God let so many children die? How was this part of a greater plan or purpose?
On top of that, I didn’t know how to deal with the information of an infant passing–when they were perfecting healthy and normal otherwise. The weight of that knowledge laid heavy on my heart. What if Isaac had been healthy–but I lost him anyway?
But Isaac wasn’t healthy. For months Aaron and I went to devastating doctor appointment after appointment. Every time we went it seemed as if there was more bad news. Another solid nail in his tiny coffin. Each hospital visit was just more evidence that our sweet baby boy was not going to live–no matter how much I wanted him too.
I never really got to dream for him. I never got a baby shower. I wanted one. I never bought him a crib or clothes or very many toys. I never decorated a nursery or planned outings for Audrey and him. I never pinned fun baby boy things on pinterest. I never got to hope past birth. So even though he was taken–just like those other babies were–I never even got to hope for a life with him.
I tried anyway. So many times I thought that maybe all the doctors and ultrasounds and hospital visits were just wrong. Maybe, just maybe, my baby didn’t have trisomy 18.
But he did have trisomy 18. And sometimes in the thick of everything that happened, it’s hard to remember that is why he died. My baby had a chromosomal defect that many doctors say is just “not compatible with life”. My baby had a third 18th chromosome and that third chromosome took his life. It’s why I didn’t know how to relate with people who told me stories of how they had also lost a little one.
I had another experience the other day that caught me off guard. Someone off handedly joked about people being retarded. I wanted to scream that they were talking about my son. I didn’t, because I knew they didn’t mean it in the way the said it. However, it still was more personal than it ever has been in the past. Jokes about having a third chromosome have never been funny to me, but there is no humor now. Having a third chromosome took my son’s life. Had he lived, he would have been severely mentally retarded. It’s not a joke that I can ever take lightly now. Not that I should have in the past–as I am positive that I have called someone or something “retarded” before. But now. Now those words cut so much deeper–they hit so close to my heart–they could easily be mistaken for physical pain.
My son changed me. My sweet little innocent boy, although perfect now, was not born into a perfect body. His body held him captive and death was the only way to be free of life’s trials and others thoughtless comments–such as the careless joke of being “retarded”. I am certain this person had no intention of offending me, my little boy or anyone else–but that’s the problem, right? We need to have more care and consideration in our words and actions.
I am at a point now where I don’t know how to live my life. It’s still all too soon and new to feel like I have “moved on”, yet remaining in the dark despair is exhausting. It feels wrong to be happy. It feels wrong to laugh and have a good time–but I KNOW that is what Isaac would want for us. He is, after all, our gift of laughter from God.
I am grateful for Audrey and moments like these. She is just a beautiful ray of sunshine that cannot be darkened. Her smile, her laugh, her infectious giggles and personality forces us to smile and remember we have so much to live for.
I still don’t know what to say to people when they ask about our family. My body is shrinking and I look less and less like I just had a baby (minus the fact that I still have extra weight–I don’t look like I do). Soon I will have nothing left but the short sweet memory I have of holding him in my arms.
It’s a surreal world I live in right now. I don’t know how to react to life. Tears come out of nowhere and yet other times when I talk about him, I feel like I’m talking about someone I used to know–a long time ago–no emotion at all. I long to feel his presence. I wish I could feel him constantly around me. I wish I could wear his memory like a warm fuzzy coat, constantly engulfed in his company.
Aaron and I had a long drive back to AZ and our topics of conversation were everywhere. Different things would trigger our grief and we would both find ourselves hit with emotions that seemed out of no where during normal conversations. What got me was talking about future family vacations. It seemed hurtful to plan fun trips without our little boy. I had a hard picturing have fun at the Grand Canyon or visiting Tombstone, when I couldn’t factor Isaac into that picture.
I know that my life has been altered. I am on a new road and there is no back tracking. I can never be who I was. I will always be Isaac’s mama and my experiences in relation to him will continue to mold and shape my life.
While life will go on and many will never know that I am the mother of an angel, I pray his existence and example will continue to mold and shape me into a more perfect being–worthy of his celestial presence.