The Paperchase Is OVER!

We received our I-171H back from CIS on Monday (June 26th). It only took them two-and-a-half weeks to process and send it back to us!!! Actually, we received TWO I-171Hs because we had said we were open to taking twins, if they’re available, although we didn’t directly request twins. So, yesterday we had copies of the forms notarized and fed-exed all the remaining documents to the agency. Now everything is out of our hands. It should take a few weeks to have the forms certified and authenticated (which we paid the agency to handle for us), then we’ll be DTC. Probably LID in early August…?

Posted by SBird - 06.28.2006 - 1.03 pm

The thing about adoption is…

that by the time you figure out you’re ready / willing / committed / open / thrilled to do it, you’re ready for the child. And then you have the paperchase. And then you have The Wait.

What I mean is that when people apply to an agency to accept them as a potential adoptive parent, they’re already there…they’ve already done the hard work to get to that point. Nobody’s filling out adoption applications when they sign their marriage certificates or turn 18 or enroll in their first 401K, and then spending the next couple years deciding whether to go through with it while they wait for China to go through its process. The moment they fill out the applications they know they want this.

I don’t think that’s true for pregnancy. I think a lot of people either just find out they’re pregnant haphazardly and then take the next eight months to get used to the idea, or they plan the pregnancy to a degree but are so validated in their choice by the culture-at-large, that, in many cases, they never really consider the implications. Adoptive parents do that sort of soul-searching before they ever fill out an application, but then they’re STILL forced to wait. That’s what I call cosmically unfair.

Posted by SBird - 06.26.2006 - 4.04 pm

The Pain Olympics

Several years ago, this post The Pain Olympics became a huge hit in infertility blogland, discussed, reposted, debated, so forth. It still pops up from time to time (as it did recently on my high-FSH bulletin board) and has gained a minor cult following–certainly the term “the pain olympics” is a neologism that has stuck, at least among infertiles. The gist of the argument is that each person’s pain is subjective, unique–to them, to their circumstances–and therefore can not/should not be judged objectively. That is, there is no comparing pain. It all sucks, and we can not begin to try to ascertain whether one person’s loss or grief or predicament is worse (or better) than anyone else’s.

Bunk, I say. Hooey. This perspective SOUNDS good, it SOUNDS like a reasonable path to tread, but in my opinion this is the easy way out. It reminds me of when I would ask my students to enter some debate, and they would attempt to opt out by using a sort of radical relativism: well, we’re all different, so who knows? /well, he’s entitled to his opinion/ his opinion is just that, an opinion/ his opinion is his own, etc., etc. Now, don’t get me wrong. I consider myself a radical, and I consider myself a relativist insofar as I deeply distrust absolutes . . . but this sort of solipsism drives me up the wall. I suspect that those who trot it out are simply unwilling to do the hard thinking it would take to come up with some viable answers to questions like, How do we categorize pain? How do we experience pain? What sort of pain is the worst sort? How does a person’s processing of pain either maximize or minimize their experience of it? People who work in certain fields–bioethics comes to mind–are forced to do this sort of hard analysis all the time. What are the rest of us scared of?

I think we’re scared of admitting that our pain might, just might, be less pain than someone else’s. My deep suspicion is that we all want to win The Pain Olympics because then we are entitled to the sympathy and coddling that attends The Victim. In gaining victim status, we gain self-entitlement. This is why so often when you are in the midst of experiencing some pain–a death in the family, for example, or an illness–you suddenly are confronted with any number of people who want to tell you their similar or not-so-similar stories. I know what you’re going through…last year, my Aunt Matilda died of lung cancer and….

Some stories might be welcome, especially those that closely reflect your own pain or come from people who really DO know what you’re going through because they’ve gone through it too. But what often happens is that people who really have no idea about the extent of your pain try to claim that they, in fact, do. They can’t stand to lose The Pain Olympics. I would rather NOT validate the person who absolutely needs to be related to me in pain by saying, yes, I can see how your nine months of infertility and my 12 years of it make us soul-sisters in pain. Although I agree that everyone has experienced some loss and thus felt some degree of pain in life, not everyone has experienced the same amount of pain, and I think that should be acknowledged. It should not be a problem for someone to admit, I can’t possibly know what you’re feeling, or, This situation is worse for you than for me, and I’m sorry. Perhaps each of us IS a unique individual, but that uniqueness is not an absolution.

When my friend T. lost her baby girl at the age of five days, I could not imagine the horror she was going through. Even though T. had no trouble getting pregnant, planned it down to the week she was going on sabbatical, and I had been struggling to get pregnant for 11 years at that point with no luck, I recognized beyond a shadow of a doubt that her devastation was so much worse than mine. Period. And even when I ended up miscarrying two subsequent pregnancies–at five and at nine weeks–I still knew that her loss was so much greater than mine. And even when T. ended up delivering a healthy baby boy last month, and I still have nothing to show for my attempts to conceive, I would still argue that her pain has been worse.

I also know that I cringe when my friend M. threatens to throw herself off a bridge if she isn’t pregnant by the time she is 30, after only nine months of trying to conceive. Her sense of what’s earth-shattering when it comes to infertility galls me to a certain extent. There have been times when I have wanted to scream at her, Talk to me when you’re 39 and have been at this for 12 years and have at least two miscarriages under your belt. Then you can rant and rave and rend your hair. Yeah. Of course, I am extremely supportive of her because that is what sane people do when they are in community with other people. We do not point out that perhaps your negative pregnancy test this month is not the same as my miscarriage this month, even though you are carrying on as if it is. We simply smile and nod and go home and write on our blogs.

For me, it’s NOT impossible to make distinctions between the degrees of pain that people have experienced. If someone actually wants to try to compare infertility to cancer (and this happens all the time), then I assume there’s just something Wrong. With. Them. There is no way infertility compares to a potentially life-threatening, terminal disease. Argue all you want with me that infertility is “the death of a dream” and that “an unfulfilled life isn’t any sort of life at all.” Bunk. You are in the midst of struggling with the expectations you had for your life, which are not coming true, at least not in way you thought–you expected–they would. But you are consumed by your sense of victimization if you can’t see clear to acknowledge that your problems conceiving a child are NOT akin to losing your life.

Many women on the bulletin board I participate in make the rather clunky point again and again that secondary infertility (when you already have one bio child and are trying for another) is EXACTLY THE SAME as primary infertility. I have to admit, this one drives me crazy. I wish they would just post on the secondary infertility board and leave the rest of us alone. Because it is NOT the same. There is just no way. I accept and believe that these women experience tremendous pain that they can not create a sibling for their child, but my God, they HAVE a child! Hello??? Why can’t they just say, this really hurts, but it is categorically different from the hurt of not having any child at all?

Many women on the bulletin board I participate in are unmarried, unpartnered women, who would love to be in a fulfilling relationship such as I have, and also have a child. They don’t have a child (like me), but they don’t have a husband/partner either (unlike me). Their pain might very well be much, much worse than mine, given that information.

The original blogger of The Pain Olympics makes the eloquent point that “it’s not about where you fall on the Bell Curve. It’s about getting off the Bell Curve.” I appreciate her perspective, and it does sound very understanding. But if you read other entries in her blog–the one where her best friend has to remind her that some people (namely the childless best friend) are envious of her one child, for instance–it’s clear that the blogger recognizes that her pain is not as bad as some other people’s pain. Okay. Good. So, again I ask, why do we have the need to level the playing field? What do we gain from “getting off the Bell Curve” and claiming that pain is All One?

I fear that our refusal to quantify our experiences with pain originates in a profound sense of disconnection from each other. That the only way we can relate is if we all come from the same place, if we’re all on the same footing, so we create a false sense that we’re all United-in-Our-Pain. But that’s not true. We experience different levels of pain based on different experiences of it. We should be able to commiserate with each other despite those differences. It demands complex thinking to figure this out, an allegiance to complexity. It is not as simple as insisting that it’s all the same. It just isn’t. And it just shouldn’t be. I have more respect for the people who have been dealt more pain in this life than I have than to try to equate our experiences. Instead, I want to listen to them, so that I can learn.

By the way, the link I posted above contains a quiz, with cumulative points, to try to “objectively” assess your degree of pain when it comes to infertility. It’s satire, of course, since she is trying to make the point that such an objective assessment is impossible. But lots of people took the quiz, nonetheless. I scored 6,150. I took silver.

Posted by SBird - 06.21.2006 - 1.45 pm

Patchwork

So, it’s June. I’m learning that I’m not posting on this blog as much as I thought I would, as much as I’d like. I’m reading a lot of other people’s blogs these days…but not getting around to keeping mine in tune with the times. I suspect that’s because life-things have shifted quite a bit in recent months. I’m doing one thing, thinking about one thing, blogging one thing, and then things shift. But I could attempt to gather together some pieces and update the blog that way…a bit like a patchwork quilt…

Patch #1: The first weekend in June, we drove to Durango (Colorado) for my stepson’s graduation from high school. Considering we spent a fair number of years wondering whether he would ever graduate, this was a momentous occasion.

He is 19-and-a-half, so a fair bit older than most graduating seniors, but he gave a wonderful speech (all the grads get to speak since the school is small and there were only 10 of them graduating this year). Several of the kids (including D.) had to negotiate the minefield of mixed families, including one graduate who had both his adoptive mom and his birth mom (who he called his “maiden mom”–or was it “made in mom”?) there. But everyone in our group behaved, and we got through it–not necessarily the most predictable outcome. I came into the family when D. was 12, and because of his mother’s violent behavior and alcoholism, his father had been awarded full custody in the divorce. So, it was stepmother mode from Day One for me. But D. is a good kid, who got lost in drugs and alcohol along the way–a combination of genetic predisposition perhaps and a difficult relationship with his mother, who continued to engage in some pretty abusive behavior toward her kids. In particular, I remember the day I picked up the phone extension and heard her screaming “loser, user, fucker” to D. over and over because he wouldn’t agree to do something she wanted him to do. Sigh. And so it goes. But we got through the weekend, and now D. returns back here to attend college in the fall. He’ll live in his own place, though, which I think will continue to provide him the independence he needs to foster his self-esteem.

Patch #2: We got the results back from our genetic testing of the “products of conception” recovered in the D&C. It was exactly as I had felt it was: 46, XX. Normal Female Karyotype. You can even go back and check me on this blog–when I first announced the miscarriage, I wrote down the baby as a “her.” I knew it was a girl, and I knew she was normal. I was very cautious to ask my OB before the D&C about whether I could trust a test result that came back “normal female”–I didn’t want to wonder whether they had tested MY tissue instead of the baby’s or the placenta’s. She assured me that I was late enough in the first trimester to yield the quantity of tissue needed to do an accurate evaluation. So, for me, I am confident this test result is accurate.

My RE is not so sure. He thinks there was still a genetic problem with the fetus that went undetected in the testing because he is so convinced my problem is poor egg quality from high-FSH and advanced age. I am having the tissue sent to another lab for a different sort of evaluation–an evaluation of whether an immunological problem–like a clotting problem–could have caused the “fetal demise.” I am not telling my RE about this additional consult, or about any testing they might have me do, or about any meds they might put me on. One of my IF internet friends commented to me that, “you know you’re an IF veteran when you start fibbing to your RE.” So, now I’m a veteran. No more newbie. No more amature. Twelve years trying to conceive (across two marriages) and one solid year of IF treatments gets me promoted.

Patch #3: We will attempt IVF #3 in August. Meds start in July. I am determined to be more relaxed this time, have a piece of chocolate, have a glass of wine.

Patch #4: I am thinking about the adoption all the time. I am thinking that whatever happens with the IVF really doesn’t matter because I will be a mother. I am thinking that the wait times are beginning to scare me they are getting so long. I had resigned myself to another Christmas without a child, but suddenly it’s possible that it might be TWO more Christmasses before we would go to China…the referral times are taking that long. Can I really manage to wait until 2008?

We had our fingerprints taken last Wednesday…this was the big-time, FBI-assessed set of prints that they take digitally on a computerized machine. It’s a little like having your fingers xeroxed. R. hated the very idea of Homeland Security being involved in getting our daughter. The fact that we need them to do this…but it is the LAST THING in the process. Once we get their approval (the I-171 form), then our dossier can go off to the CCAA at long last.

Posted by SBird - 06.12.2006 - 1.33 pm