This post, sequel to Congenital Hypothyroidism: The Past is not about the Boychick’s future — which is as unknown to me as it is not my story to tell — but about how his condition (or rather, my experience of it) is affecting this pregnancy. To understand any of this post, you need to have read part one first.
I don’t know how much I can express just how much of our lives were shaped by this one tiny pill, this one glandular lack. I don’t know if I really knew it myself, at the time. There was no going out in the evening, because he needed to be pilled. There was no going out on the weekend, because he needed a blood test (every two weeks then every month for most of his first year) and I needed a day to recover after, a day with us naked and alone and in our cave to remember his perfection, to fall in love with my baby and not be afraid of his diagnosis, to apologize for the screaming and the tears and the blood and the pain of the previous day. Everything was touched by this.
I do not know what a “normal” infancy is like.
Congenital hypothyroidism is not a disability — because he started supplementation by one week old, and maintained good levels for all but tiny wobbles here and there, quickly noticed and corrected, his development has been apparently entirely unaffected by his endocrinological dysfunction. Congenital hypothyroidism is the most common of the endocrinological/metabolic disorders that newborns are routinely screened for, at roughly 1 in 3000 infants. It’s hardly a “special need”, even, because, when caught on screening, there are no therapies, no neurological tests, no expectations of atypical adulthood, no comments from other parents, no questions of how he acts or looks because he acts and looks the way we, ableist people that we are, expect children to. By adulthood, unless supplement-resistant, hypothyroidism is hardly even a chronic illness — I have adult-onset hypothyroidism, as do half a dozen others my age I could name, and more in my parents’ generation, and it’s nothing. It’s a pill, once a day, a blood test, every four months starting at age 3, repeated until he dies. It’s nothing, now: he chomps his pill, we mark the calendar for that one weekend sacrificed to the vampires that ate his infancy, and we move on.
But then — then, it was everything. And I had nowhere to turn, not really. I could peek into the lives of “special needs” parents, could pick their brains for tips with pills and blood draws and doctor-office phobias, but I was to grow out of that need, to have a child with a life ever less affected by his anomalous body. I was welcomed graciously into their home, but I was a guest only, though I’m still not sure whether that discomfit came from them or, more likely, me.
It is this that part of my brain keeps coming back to as I think about the new life I’m gestating, as I’ve thought about the infant we’d been trying for: the accouterments of infant life to me include shot glasses and baby spoons, pill crushers and prayers for a spit-up-free evening. I imagine life with the newborn, and those things are there, and I remind myself, again and again, that that is not every baby. That is not most babyhoods. The odds of that happening again are astronomically small.
And I think, what will it be like to have a child who is different — a child without the pills and the pokes, for ze will be the different one to the normal of my firstborn. What will it be like as this little one grows up, and hir older sibling sees a baby, a toddler, a child, who doesn’t need to go to the phlebotomist, who doesn’t have a standing order at the lab, who doesn’t learn to spell hir name from listening to us leave refill requests at the pharmacy?
And, more hiddenly, what if the endocrinologist is wrong, what if the doctors and pharmacists are wrong, what if I did somehow cause his disease? What if I created his defect with my own defective thyroid? What if this infancy is exactly like the one before, but with an older child to care for now also? I have insurance, this time around — we will not be parceling out my own thyroid testing, balancing the recommendation for monthly testing with the need to eat and pay the midwife. But there it is, still, the worry — what if?
There is so much more I could write, questions I have: how do I be a disability activist, and work so hard to make sure my child is “normal”, “undamaged”? how much did his diagnosis contribute to what retrospectively I recognize as PPD and PPOCD? There are feelings I cannot put into words, worries my mind focuses on without having names for, feelings of dread and longing and fear and the past-futureness of not being here now, of being afraid to be here now because something might go wrong then, of the belief in Murphy I know is ridiculous and I know I will never shake and that makes we want-notwant to name all the things that could go wrong so that they won’t.
But mostly, there is grief: for the infancy my firstborn did not have, for the babymoon I only half got (the memory shattered and overshadowed by the shrill ring of that first call), for the fears and worries of my past self, for the scared child inside my psyche now, worried about the bean nestled in my pelvis, wanting to get to the end, to the time four years later when what is agonizing now will be a pill swallowed happily and the calm of experience that it all turns out just fin eventually.
Even if this baby’s screens — for there is no question now whether there will be any — come back normal, I will never know what it would have been like to have the Boychick not have congenital hypothyroidism. I will never have that time again, will only experience an entirely new babyhood with its own perfection and agony, its plans discarded and reality adjusted to. And that’s no different, really, than what any new second-time parent goes through, that knowing that each child will be different, that for all we give birth “again”, it’s to a whole new baby, and it’s a whole new experience. It’s no different from what everyone else goes through.
And yet, in some ways, it is.







Pregnancy Massage I, take 2: in which I beg for woo and e-support
If things’ve seemed quiet around here, it’s for a good reason: things have been very not-quiet in my life. Nothing much more than usual: started the term with a two-massages-a-week class, lost preschool for the child1, met a stranger and asked her to put her hand in my cunt2, and, today, started the three-day intensive for Pregnancy Massage I. Again.
It’s been six months since my back went kablooey3, and I’ve spent hundreds of hours and hundreds of dollars working on getting better, getting well, getting strong, and I don’t know if it’s enough. I don’t know if I can do this course, and I don’t know if I can have the career I’ve spent the last two-plus years working toward if I can’t finish it.
There’s a lot I’m doing differently this time4, and I’m not in the same place I was then, but I am terrified. And I’m doing all the woo acceptance I can, acknowledging the fear and letting it go5, staying in just this moment, grounding myself and feeling and loving my body as it is — but the fear is still there.
So this is me accessing all the resources at my disposal, and asking my community for support.
Tell me it will be alright. Tell me I will get through the weekend. Tell me I’ll still be a massage therapist even if I don’t. Tell me I’ll still be worthwhile human being even if I don’t get my license. Don’t tell me things will happen as they ought, but that I have the ability to make things work out whatever happens. Whip out as much woo and as many cyber hugs as you got, and lay it all on me.
And soon6, I’ll get back to my usual, less needy, more pedantic, kyriarchy-kicking ways.
Whether or not my spine stays whole.
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