The last couple of days have been wrought with some downright scary thoughts. I’ve traveled to some pretty intense destinations within my mind, and well, I’ve really wondered how I would ever claw my way back from the pit I’d fallen into. I am that deep in this pit of self-loathing right now that I am starting to wonder if there is anyway to get out of this thinking, or out of this feeling.
You see, I fell into this pit last year. When I sat down with the agency worker, who delivered a set of news that rocked my world, and caused me to hate myself more than I had ever hated myself before. I told some people what I was told that day- my therapist who watched me crumble in away that I have never let anyone see me do before, The Hubby, my best friend, and my parents. I later spoke to some experts in the field to find out details that hadn’t been included in the information I was given, and spoke about my reservations. Although, after that initial day, I refused to talk about it, and just shrugged it off. It has been something I have thought about almost every day for the last year.
The message I got whenever I spoke to people about this was, “Be honest and tell them your opinion”. I scoffed, I laughed. Why would I want to be honest now? I mean, I know that’s who I am. I’m an honest person. But this? This news about The Kiddo? I would never want to be honest about how I feel about this diagnosis. I would never want to tell the truth about this diagnosis, because it makes me sick.
Here we are a year later, and honesty still appears to be the silent message I’m being told to voice. My best friend told me in her sage wisdom that I had to do it, if not for me, but for him, The Kiddo. I needed to voice my opinion, even if it meant dealing with some consequences. I needed to tell the truth, so one day The Kiddo would know how I felt, without any question or doubt.
That has been sitting at the back of my mind ever since my visit with The Kiddo’s parents on Sunday. Could I finally be brave enough to voice my opinion, and say what I need to say, without fear of all that I stand to lose if I articulate my truth?
You see, I went into the visit hopeful that we were going to start a new chapter of openness. The Hubby told me not to get my hopes up, he felt like our relationship with them would not progress to more openness for years, if ever. I disagreed out of sheer desperation. I needed to see a hope for openness, because otherwise, I was beginning to wonder why I was even around and why I was torturing myself.
During our visit, as they said that they would likely not introduce me for another three or more years, I nodded, and hoped that my devastation didn’t show on my face. I quickly did the math in my head. He’d be 12 then, at the earliest. The window of opportunity to have this reunion be a positive one seemed to be slipping through our fingers. I wanted to ask them if they realized that, or if they understood how old he’d be at that point, and how that would dramatically play into the dynamic. Furthermore, in three or more years, he’d know about his diagnosis, and I can only assume the resentment toward me, would be high.
I respect their decision, I have to, even if I don’t understand it. They say that he’s immature, but then they tell me stories where he is more mature then some adults I know. I have to wonder if they are just not ready for this, if they don’t want it, and maybe can’t find a way to articulate that they want me to disappear. Their hesitation baffles me.
And of course, I respect that they are his parents, and when it comes to this relationship, they are in complete control of what happens. Even if I would do it completely differently.
But that window, I see it in my mind. It’s the reason why I have kept quiet and not outwardly said what I really think of the diagnosis, or how I really feel. It’s the reason why I have smiled and nodded, even when I wanted to express disappointment. It’s the reason I have bit my tongue, and only cursed in the safety of my own home. There was always a tiny sliver of hope that indicated that I might be in an open adoption sooner. Now, I’m being hit with the realization that the window is closing, there is no chance of reunion right now. I may have been silly to think it was ever possible before adulthood. I know how things work in the LDS faction. A full, honest, constant open relationship through adoption? It’s rare. It’s unheard of, and I can’t imagine, in this particular situation that The Kiddo’s parents would be willing to be blaze a trail for those to follow.
So, I’m admitting defeat.
Instead of hiding in shame, I’m going to be honest, because that’s what I have been trying to do all year. I have been trying to change my routine, and open up. This honesty isn’t just for the world to read, it’s for me. So I can heal, so I can move on. And I hope that is what this confession does for me; I hope it sets me free. Right now, hiding it is eating at me in a way I’ve never had something eat at me.
The Kiddo was diagnosed last year with Fetal Alcohol Syndrome, or more accurately, Alcohol Related Neurological Defects (ARND).
I do not agree with the diagnosis.
I don’t agree with it for a number of reasons, namely, based on the amount of alcohol I consumed it doesn’t make sense. Based on when I consumed it, the diagnosis doesn’t make sense. When I got the diagnosis, I did reading, a lot of reading. I didn’t fit into the criteria of what most professionals would qualify as a legitimate reason to diagnosis with such a heavy label. So then I got my journals out, because I wrote a lot back then and because I wanted to verify my statement that I hadn’t drank more then two coolers, and that it had been terribly early, possibly before conception. I figured out when my last period was, I figured out when A and I broke up. I figured out the dates when I drank each of those coolers.
Here’s the reality:
One would have been before I was even pregnant, the other would have been just shortly after, maybe a day or two. That particular cooler? I didn’t even finish. I had it as a nicety when I sat down with A’s grandpa to chat, and he razed me about not finishing it and wasting alcohol.
Yes, I know that any amount of alcohol is too much, but this? It just seems like too much, like the diagnosis doesn’t fit the crime at all. Like it was the easier place to go to, when they were struggling. Because it meant it wouldn’t be their fault. It was an outside person to blame, or an outside occurrence. And I guess, maybe that all makes sense after years of struggling with him behaviorally.
When I was pregnant, I spoke to friends who were medical professionals, and I asked them about the drinks. I was reassured, and even laughed at for being so worried. I was told, “There are women who drink way more then that, and their babies are just fine”. I was told, “That’s so little, it doesn’t even count.” I was told not to worry. I was even advised not to put it in any paperwork, because it wasn’t even something that should be considered, if they ran into behavioral issues.
That part of the paperwork was the last thing I filled out. I stared at it for days. I wondered if I should put it in. I had conversations with myself about it. I felt like I should out of sheer ethics, but something told me not to do it. The agency worker told me I had to and I had a feeling if I didn’t put something in, that it would end up there anyhow. I prayed about it, and the feeling was that I should leave it out. I hated that damn question and the line that sat empty. In the end, I ignored my gut, and I filled it out.
In the paperwork it says, “In the first 2-3 weeks of pregnancy” to the question about consuming alcohol.
When I said that, I was counting from the time I had my period. Not when I found out about the pregnancy. And then, below that, there is an addition. Because that’s all I wanted to write. Because I had been told it wasn’t even necessary to be there. Yet, when it came up, I was told that I needed to put how many. The worker convinced me that I should err on the side of caution and say more than less. When I said I knew exactly how much I drank, and when I drank them, I was told that I may have forgotten from all the stress I was under, or from that “darn pregnancy brain”.
I trusted her. And I trusted that it was the right thing to do, being honest, but then I was asked to elaborate, because even then, I trusted that they might be right, that they might be right that I could be wrong. Because my self-worth was so low, that I believed that I couldn’t even possibly remember something that occurred just months before.
I feel like I was set up. And used. And now, The Kiddo lives with this label, a label that I know he wouldn’t have if I had parented him. A label that will follow him for a life time, and will cause him to look at me much differently when we are reunited, even though my opinion or experience was not a part of the actual process of coming to the diagnosis. A label that will cause people to judge him and reject him, over and over throughout his life.
Of course, it’s only my word, the lowly birthmother word. I wasn’t included in this epic diagnosis, when they had access to me, and know I would have actively participated. My gut tells me I was kept out for a number of reasons. I have thought of many of these reasons over the last year and I have wondered how I could articulate my disappointment. Because that’s what it is, regarding how this was handled, and how I was left out of the entire process. And what it means for The Kiddo, for the rest of his life.
Really, that’s what it is, complete disappointment. I’m not angry with them. I’m not even mad. I could be, and I know that’s where my parents went when the diagnosis was given out to us. I even protected and stood up for The Kiddo’s parents when my family was saying uglier things, because I don’t believe that this diagnosis was ever vindictive. I believe they were in a place of exhaustion, and that paperwork was just there, with information that could explain away his behavioral issues. I get that, especially now as a parent, the struggle and inward fight that happens when you are not quite understanding why your child is not behaving in an appropriate, normal manner. I get how frustrating it is when you just want help, an explanation, an action plan so you can move on with your life, and stop revolving around this one person who is monopolizing everything.
What I am angry about is the fact that all of this would look entirely different if I had been strong enough to parent, and not stupid enough to believe every word I was told through the agency or fall for my parents routine manipulations. What I am angry about is having parents who saw religious resitituion as the most important aspect of the scenario, versus keeping The Kiddo with me.
Most of all, I’m angry that I was lied to in the hospital. When I cried over and over, and over again that he was going to hate me, I was told he wouldn’t. I sobbed over it, I begged him not to hate me, as if he, as an infant understood. I felt so sure that if I went through with this adoption that the end result would be hatred. That he would hate me.
Right now? I feel like I was right. How could he want anything to do with me, if he finds out about me around the same time he’ll find out that his “brain is different” because his biological mother consumed alcohol. I am the reason, according to this diagnosis, that he struggles, that he will struggle. I am the reason why his life is a little harder. Why wouldn’t he hate me for that?
Of course he’ll hate me. His parents will be the saints who parented him through, and I will be the dumb teenage girl who got knocked up out of wedlock and consumed alcohol, thereby ruining his life.
I ask again, why wouldn’t he hate me?
If I’m continuing the trend of honesty, for the last year, I have hated myself, I have hated everything I am, to the point where I have lost confidence, any ability to maintain self-worth, and I challenge any person who even remotely says they love me. If I hate me, why would he have any reason, especially since I keep being shoved back to the shadows, to not do the exact same thing?
I hate me not because I believe in the diagnosis, but because I wasn’t smart enough to know that I shouldn’t have been so damn honest, and trusting. Because I have continued to believe that my voice is an important one in this equation.
And I am learning, even nine years later, that while I was told I was the most integral part of the process, my time has been served, and my opinion, even if it serves the truth, has no part in this adoption process past the day I signed those damn papers.
That realization alone is enough to keep me paralyzed in this pit of complete self-loathing for an eternity.





