Tag Archives: Health

Congenital Hypothyroidism: The Future

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.

Congenital hypothyroidism: the past

Although I’ve mentioned it before, I’ve never explicitly written here about my experience with the Boychick’s congenital hypothyroidism, and how it affected me as a parent. This post will be published in two parts: The Past, and The Future, because when I finally sat down to write about it, more than 2000 words came out — apparently I’d needed to. Both parts are written; the second will be published tomorrow.

The Boychick has congenital hypothyroidism.

When he was a week old, we got a call that his metabolic screening panel came back positive for congenital hypothyroid. I think this call, this first pronouncement, was from our midwife, but I don’t remember her calming tones, her everything-will-work out demeanor: I remember the blood in my ears, the grip around my perfect child tightening, the irregular shape of the bricks outlining our empty fireplace. There were more phone calls after that, to or from the endocrinologist, to a rapid succession of health care practitioners as we scrambled to answer the question “Who is the child’s pediatrician? We need to know who to send the results to.” Pediatrician? We don’t have a pediatrician! We weren’t supposed to need a pediatrician — the midwife follows him up for the first two months, he isn’t going to get vaccinations right away, and well-baby visits are pointless! And besides — ever mindful of the lessons learned at my MD mother’s knee — family doctors are for babies! We just haven’t found one yet! But apparently, we had to, and soon.

We got the call on, perhaps, Friday? He was born on Thursday the week previous. One week we’d had with perfection — the most perfect baby ever born, perfect smooshed nose, perfect hematoma on his perfect skull, perfect grey-blue eyes, perfect long toes with perfect tiny nails, perfect red “angry baby!” Hulk impression, perfect everything — and now we were told it was a lie, that he was broken, defective, lacking, and so were we, since we didn’t even have a pediatrician for him. He had never been dressed, never worn more than a prefold diaper Snappi’d or wrapped around him, coverless to learn his elimination patterns. He was our Naked Baby, our perfection incarnate. And I had failed him.

We were told, at first, he’d need a follow up blood test on Monday, and a pediatrician today. Within hours we were told no, he needed the test now, today, and a script for thyroid to start today just in case it wasn’t — as the odds were in favor of — a false positive. A week of extra thyroid for the false positives, the endocrinologically typical infants, was worth the week of not-delayed brain development for the true hypothyroid babies.

I don’t remember who called the orders, who chose the lab, who told us when to show up. I remember getting him dressed that first time, remember the green onesie with the yellow duck patch sewed on, remember it hanging unsnapped over the brown wool shorts I’d knitted for this perfect baby, the red Kissaluvs diaper underneath. I remember it was the first and only time we used the diaper pad we’d went out and bought a dresser for (instead of the usual other way around — we’ve never done things normally in this family). I remember the drive to the hospital, the crisp clarity, the unreality, of the world outside; remember marveling at the green on the trees, as Oregon had slipped from winter to spring while I hibernated, naked and content in the dark, basking in the light of our own explosion of life. I remember the sway of the car as I sat in the back, on the side that had no buckle in the car we couldn’t afford to replace or repair, heedless of my own safety, heedless even of the physics of my baby’s safety in the rarity of an accident, because it would have taken much stronger forces than gravity and inertia and momentum and seatbelt laws to pry me from his side. I remember leaning over his car seat, staring at his perfect face, still so slightly bruised from the birth, telling him everything would be fine, telling his father to drive slow because everything felt so fast, caressing his perfect hand with their extraordinarily tiny-huge fingers. There had never been so much, so many barriers, between us.

There was a blood draw, which he slept through, lying on a table with me sitting at his head, The Man at his feet — in socks? those tiny leather soft shoes, the first baby purchase we had allowed ourselves to make? — his fragile-seeming infant arm in the phlebotomist’s hand, his blood running in a tube from the still-vernixy crook of his elbow to the vacuum phial in her other hand.

We went home, and I ripped both our clothes off and dove into what had become our chair. I couldn’t eject the reality of his positive test from our lives, but I could and would and emphatically, immediately did shed from us the barriers between us it had required. Naked again, right again, I held him and nursed him and cried into his sweet-savory-sparse hair.

The follow up results came back, and they were very, very positive, and we were very, very grateful — though not exactly pleased, for all the stress it had brought into our lives — we had chosen early metabolic screening, had agreed to prick our newborn’s heel not once, at a week, but twice, the first at three days, giving us the results within the seven days required for supplementation to start, for future brain damage or deviation to be undetectable.

Eventually — probably within the week, but I could no longer say — we met the pediatric endocrinologist, a woman I, nearly four years later, still adore, who explained she would be happy to either consult if we selected a primary care physician for him, or would take full responsibility for this part of his care, would order the tests and prescribe his medication, would chart his growth and answer our questions, would manage his dose and his condition with the full power of her experience and expertise, and it would be up to us and the luck of childhood illnesses whether he ever saw another care provider at all.

I wanted to slap the first responder, who had demanded the identity of “his pediatrician”.

Our days came quickly to revolve around his little daily pill. Torturously, the initial dose — higher to make up for the week without any thyroid at all, as his ability to leach umbilically from my supplies dried up with his cord — was white. White, the color of milk. White, the color of his copious, many-times-an-hour spit up. We would have a spitter, of course, because that’s exactly what every needs-daily-medication baby should be.

If he spit up the pill, we had to repeat it. If he spit up, but there was no pill, there was no need. So we would call our endocrinologist and ask, does he need another dose? And she would say, can you see any pill? And we would answer, the pill is white! And she would say, oh, that is tricky. Well, if he doesn’t spit up for the first fifteen minutes, it should be fine. And we planned our days around this dose, his spit up, the availability of The Man to be there, for he, always, would give the pill — I would express into a shot glass (one month old, and our child had his own collection of shot glasses), and The Man would crush it, and scoop up my milk, and tap the powder — careful not to lose any to stray baby kicks or an errant sigh — into the milk, and maneuver it, so carefully, into his mouth.

(There were other methods we tried, at first, other recommendations — medicine spoons, and syringes, and pre-mixing — and eventually we figured out the pill would dissolve entirely on its own, uncrushed, but that was the way we did it in that unending forever of the first few months of parenthood.)

And repeat, as needed, until it was all gone, the rejected drops retrieved and respooned more carefully into his mouth than any parent had chased strained carrot mash — we, who planned to only allow our baby to feed himself, had a collection of plastic-covered baby utensils to rival the most avid spoonfeeder. We suffered the surprised remarks from the checkout woman querying “Isn’t he a little young for solids yet?” as we bought yet another package, having lost so many to unwashed dishes and spoon-obsessed dogs. I grimaced, said nothing, and didn’t give in the urge to strangle her.

We would time this exercise to coincide with a wake up, after a feed and a nap, but before a feed and play time and never-ending-spit-up-time. If we were lucky, we’d get him awake and pilled and give him a few minutes of digesting before he wanted my breast and to refill that I-swear-it-was-bigger-on-the-inside stomach with the ammo for a new round of “was that a piece of pill?” and “pass the prefold, I think it got in my hair this time!”

We were often not so lucky.

Part two will address how this experience is affecting this pregnancy — and my worries about the future.

Quick hit on birth advocacy and privilege

A friend of mine (and my midwife for my pregnancy with the Boychick) shared with me The Story of Mrs Y and added:

The concern over our high cesarean and birth intervention rate is a privilege. Seriously. We cannot have any idea about how so many women face pregnancy and birth in other countries where the simple, natural act of childbearing could easily end in death — of them or their babies.

This was my take on the topic:

I don’t believe in the limited thinking that says we can or must only care about one (the “worst”) injustice at a time; we absolutely can and ought continue to work here on making birth better and safer for those facing the ridiculously, immorally, and unscientificly high cesarean and intervention rates.

But so often in USian birth advocacy, we completely ignore or dismiss the real risks of those who have no access to care, no resources to learn from, no emergency services for the rare occasion when they are truly needed, and not even the basic level of nutrition and hygiene that makes “natural” birth mostly safe.

It’s not unhindered birth when that is all you have, when it’s not an informed choice, when the midwives who had worked in your area have been imprisoned or worse, when the only other option is walking for four hours to a hospital that makes ours look humane and caring. It’s not freebirth right here in the USA when a teen has no access to birth control, no ability to say no, no way of getting an abortion, and no one to turn to who will not shame hir for being pregnant. It’s not safe or rational to consider homebirth when one’s “home” is unsafe or nonexistent. It’s not humane to shame someone for seeking pain relief for an experience they didn’t choose. It’s not reasonable to demand someone do the strenuous, “natural” work of labor when never in hir life has ze had adequate, abundant nutrition, and all hir tissues reflect the lack.

It’s not that birth practices or intervention rates don’t matter. It’s not that hospitals don’t desperately need reform, on so many levels. It’s not that it’s wrong to work on changing those. It is that we flaunt our unseemly ignorance of our privilege when we talk as though those are the most pressing needs in birth the whole world over, or that it’s only “those brown people way over there” who are still lacking what we take for granted and are seeking to move away from.

Onion

I am an onion.

I am made of layers, and peeling them back will bring about tears and pain and I don’t have the time and I don’t have the energy and I don’t have the safe space (never chop onions on a slick glass cutting board) and I don’t know when if ever I’ll get the time-energy-safety but I need it. I need to peel, to pull away the old, to be new and raw and growing — but I sit, wrapped in skin, my own dying flesh, some layers paper thin, some rotting, some bruised and broken and hurting, hurting me, holding me in.

I cannot peel them, but I have started, tried, been wounded and cut and am bleeding, and can see some of them clearly.

***

A layer: no more playschool. Running out of preschool options. Have run out of that-which-makes-it-possible-to-look (spoons, energy, willpower, willingness to overcome phone phobia, whatever it is).

Another: urgings to take care of self, and build strength, and get well, and make an appointment for this and that and now this other thing and this one also — while at home is a child screaming for me not to leave him.

Another: Holistic Pelvic Care appointment that brought huge physical and energetic shifts, bringing up memories of birth and

another: not having the words to describe the sensations then or now, and a birth story never written for want of those words.

***

And

A child, screaming, yelling, fighting, pushing me and pushing and pushing and pushingpushingpushing until I am afraid not of him but of myself, of hurting him, of losing it in even worse ways, and so I cry –

and he calms and suddenly I am five, ten, sixteen, and my father is pushing me and pushing and pushing and pushingpushingpushing until I lose it, until I am yelling just as he is, until I cry, and then, then he is calm and I hate him for it, I hate him and I hate me for giving in, for letting him win, and I am there but this is my progeny not my procreator and I cannot yell at him, not for this, and I cannot trust myself, and so I shut down.

***

I shut down.

And here I am. Shut down, shut away in the cellar, unable to be whole, unable to grow, unable to renew. Alone in the dark.

An onion, twisted. Afraid of my layers.

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.

*******

  1. The whole school is on hiatus for the health of the owner, and yes that is about as fun for everyone involved as you might imagine, not least her.
  2. Which I will write about soon, under the title “Adventures in Holistic Pelvic Care, Or, Yes You May Put Your Hand Up My Splink”.
  3. That’s a technical term.
  4. I’m not spending any time on the table, I’m not trying to force myself to sit on the floor with everyone else, I’m taking an extended lunch break tomorrow for a please-stop-my-back-from-breaking chiropractic tune-up, and I’m accepting all the help I can get with setting up the tables and moving equipment around my own body mechanics. And I still don’t know if it will be enough.
  5. I keep inviting the fear to leave, but it’s hanging around like a house guest with poor boundaries and worse hygiene, eating my food, monopolizing the remote, and generally making a mess of the place. Somewhere inside me there’s a zen master drinking tea calmly, but the rest of us are running around with bleach and brooms — cleaning up after it, or trying to chase it out, depending, and we kind of hate the lazy tea-drinker.
  6. For a certain value of “soon” approximately equaling “find an acceptable replacement for the practically perfect playschool which is now closed”.