Tag Archives: chronic illness

Let’s try that again! Send me your stories on parenting with disability or chronic illness

I got fabulous feedback and lots of enthusiasm for AP Our Way, BUT, I haven’t gotten nearly enough submissions to make a zine. So! We’re trying this again.

Send Me Your Stories

I don’t care if you don’t think you’re a good enough writer. I don’t care if you don’t have time to write as much or as eloquently as you’d like. I don’t care if you don’t think you’re “disabled enough” or “sick enough”, and I don’t care if you don’t think you’re “AP enough”.

Send Me Your Stories

I know you have them. I know you struggled to breastfeed, had to argue your heart specialists for every extra day of gestation that your neonatologist recommended, refrained from rolling your eyes at well-meaning relatives who told you you’d never be able to parent at all much less “like that”, gave up on elimination communication and cloth diapering and nearly everything else when postpartum depression threatened to overwhelm you, hated the judging gazes as you returned to work so you or your partner would have health insurance to pay for your medical care, set aside your dreams of homeschooling when you realized you’d never be able to get your child to park dates and enrichment classes on public transit. I know you have stories I’d never even guess at. So what should you do?

Send Me Your Stories

That’s right.

Now you have until July 1st (2011). I’m working up a guest post about the zine, too, so if you’d be willing to host such on your blog, let me know — or, write about it yourself.

Whatever you do (say it with me):

Send Me Your Stories

That Stinks!, or, disability exists at the intersection of the individual and society

Pregnancy1 is a blissfully neurology-stabilizing state for me. Not only do my moods stabilize (auto-comparatively…), but my migraines decrease significantly, both in severity and frequency. Which has been allowing me to take risks and perform tasks I usually don’t or can’t or am much more wary of — which in turn has me thinking about migraines and chronic illnesses and the social model of disability.

Note: whether or not migraines count as a disability per se may be up for debate (though I’d be more likely to say, are up to the individual migraineur’s2 situation and identity), but regardless, I’m going to use my experience with migraines here as illustrative of disability in general and an explanation of the social model of disability — both because I have at times in my life been disabled by migraines and because I cannot fully separate my bipolar disorder from my migraines3 (though one is more likely than the other to be recognized as a disability). The extent to which the following is translatable to any other experience of disability or chronic illness will vary, and I do not mean for it read as The One Truth About Disability. But I will say that in my talkings with others with disabilities and my readings of other disability activists, it shares enough similarities to be valuable as an illustration.

Even while pregnant, though, I am at risk of them: my migraine status at any given time (vulnerable? migraineous? active migraine? post-migraine hangover? low risk?) is always in my mind, and is always something I consider, however briefly, when planning my day.

That is not disabling.

My home, even in pregnancy, has differences from a non-migraineur’s home4, differences so ingrained I don’t even think about them the vast majority of the time: you will find here no scented products5, no striped or strongly contrasting color-schemes or curtains or clothes in our closets, no checkerboard tile patterns, no battery-operated noise-making or light-flashing toys, no energy-efficient prone-to-flicker long-bulb fluorescent lights6, no TV on in the background, no wood-burning fires (even if we had the fireplace), no slatted blinds (and very few window screens), no — for all people find this the hardest to believe — chocolate.

None of that is disabling.7

There are certain behaviors inside (and outside) my home that I engage in (or, more frequently, refrain from engaging in) because of my migraines: I rarely play video games anymore (sob!); there are many movie/TV scenes and some entire movies I do not watch, or do not watch unless very solidly in a Low Risk state (which I will likely move out of if I do watch said scenes); I don’t cross my eyes or spin around or watch others (even my child) move too rapidly in a repeated motion, such as jumping on a trampoline; I sleep as regularly as is possible with a child and a writing compulsion and a brain that often doesn’t cooperate; I don’t eat chocolate (or licorice or anise), even when available and offered and oh-so-tempting.

These are frequently annoying, but they are still not disabling.

When I have a migraine — a full-on, active migraine — I am incapacitated. I am in pain (to put it mildly), nothing in my brain works quite right, my word recall goes to shit, my cognition deteriorates (and not solely from the pain), my senses go hypersensitive and screwball (think apples that taste like sunscreen, voices that fall like hammers, scents that smell like pain, lights that I shy away from like a vampire from the sun), and I am more or less unable to do anything productive, enjoyable, or, well, anything except exist and wish I didn’t and wait for it to go away. These happen sometimes no matter how many precautions I take and reduction behaviors I engage in.

That is, in someways, disabling — but it’s also just my life, and my luck.

What is disabling, what disables me and limits my life in ways I do not find as easy to adapt to and integrate, is these:

cigarette smoke, both primary as I’m trying to get from my car to the store, and secondary as the chronic smoker walks by my restaurant table

perfume and cologne, dabbed or drenched on the person seated behind me on the bus

the laundry aisle at the supermarket — most days when non-pregnant, I can’t even walk down it without holding my breath (and sometimes, not even then)

the pattern in the carpet that seems to shift before me, that I have to walk over (eyes closed) for 10, 100, 500 feet to get to my destination

strobe lights in every dance hall, ever

bass lines so loud they can be felt without eardrums — in bars and trendy restaurants and the car driving by my house and played by the neighbours in our first apartment building

automated bathroom odor-maskers and hand soap whose scent lingers for hours, even after getting home and washing it off — twice

that one light in every classroom, every mall, every not-ridiculously-overpriced grocery store that’s on the fritz and flickers constantly

These are triggers I cannot control. These are triggers I risk exposure to if I wish to enter public at all, triggers that can make the difference between my accomplishing my goals in public for that day or not, can make the difference between being able to function again the following day or needing to hide in the dark quiet praying for death and/or sleep.

And no, I don’t expect every space to be entirely trigger-free, to look and sound and smell like my house. I would and have and will advocate for reasonable accommodations, including scent-free places, public smoking restrictions, sound limits, improved lighting, and so on, but it would be unreasonable for every possible trigger to be removed entirely from public spaces.8 The point is not that society must change in every conceivable way that would benefit me (though really, a few small changes is not too much to ask). Rather, the point is this: it is not until I step out of my home that my tendency toward migraines changes from something I deal with without much thought or bother to something that hinders my ability to go about my life.

That is when this part of me — my predisposition for migraines — becomes a disability. This disability is not inherent in my neurology, for all that my neurology not the same as the majority’s (and is frequently a pain and an impairment): no, the point it becomes a disability, that I am disabled, is at the intersection of my self and my society.

That is what I mean when I speak of the social model of disability — and why I’ll keep banging away at society’s role until ableism both individual and systemic is no longer the culturally accepted default.

  1. Or at least, both times I’ve been pregnant long enough to notice any effects.
  2. Migraineur: one who gets migraines.
  3. For three reasons, in increasing compellingness: there is a high overlap between people with mood disorders and people who get migraines, more so than either appear alone in the general population; the same drugs are often used to treat/prevent both; and, for me, stability in one part of my neurology goes along with stability in another — that is, when my moods are better, my migraines decrease. Whether or not it’s true in anyone else’s life, for me, the two are inextricable.
  4. Though I will say that every migraineur is different, with a different set of triggers, and so what is true of my migraine-reduction needs may not be true of someone else’s.
  5. No candles, no deodorizing sprays, no incense burners, no essential oil diffusers, no “aromatherapy” soaps or lotions or dryer sheets, and only unscented dish soaps, bath soaps, hands soaps, and laundry detergents; no shampoo at all, because it’s so impossible to find one that both doesn’t reek and does work (thank you baking soda and apple cider vinegar).
  6. I do OK with some compact fluorescents, as long as they’re not the only light source in a room.
  7. No, not even the lack of chocolate.
  8. If nothing else, I have no desire to be the focus of a mob wielding broken ceramic mugs blaming me for the banishment of every chocolate cafe.

Because I wasn’t busy enough: a Call for Submissions

So, did I mention that my moods sort of stabilize in pregnancy? Because this is not (I’m pretty sure) hypomania, but rather (and yes, you can be shocked; gods know I am) a glimmer of what “normal”, “regular” productivity is like. Because in addition to parenting, gestating, getting licensed and starting a massage practice, keeping up the blog, attempting to get published, contemplating buying a house, attending conferences (some outside the country) and all the other things I’m doing in my spare time, I’ve decided to create a zine:

Call for Submissions for AP Our Way: Disabled Parents Making Attachment Parenting Work for Us and Making Peace with When We Can’t

But not by myself, oh no: you all are going to help me. If you don’t have anything to submit to it yourself (are you sure?) please please give the CFS a signal boost. Post it to Facebook, Tweet it, link it on your blog, ask your favorite bloggers to mention it, post a flier in your community center, tell someone you know and think might be interested about it, ask them to tell their community: I’d love to get as many voices from as diverse a population as possible represented.

Also, wish me luck and continued stability and energy.

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.

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