Monthly Archives: July 2022

ivf day 39: a go for beanification!

i had my monitoring appointment this (monday) morning, and everything looks great, so we’re a go for embryo transfer next monday in albany! uterus is 9.5mm thick and trilaminar, and everything seems to have righted itself. perfect landing pad.

6AA is going to need a better name as a transferred (and hopefully implanted) embryo, so for now i’m going with “the bean”. monday is officially a go for beanification! (the beaninning? commencing beanitude?)

i checked my appointment portal and noted that 6AA will be thawed at 5:45am for a 10:30am transfer, so if you ever wanted to know how long a 5-day blastocyst needs to thaw… well… you’re welcome? i have an appointment for IV intralipid therapy and acupuncture at 9:30, and then the do will be done at 10:30. no anesthesia required, and stephen can be in the room with me. just an ultrasound-guided catheter up the hatch, and world’s tiniest deposit. i’m hoping there will be opportunities to take pictures of the ultrasound during the procedure, and i’ll share them here if so.

i have another acupuncture session just after transfer, we stay a night in a local hotel, and then we come home, hopefully with a beltane (may day) bean on board. i’ll have pregnancy test results by the end of the following weekend or early that next week, and i’ll be using all i’ve got to call in favorable results.

y’all, this shit isn’t for the faint of heart. but what an interesting ride it’s been so far. here’s hoping it’s just the beginning.

yours truly,

a hopeful mama

ivf days 33-38: grumble grumble

tuesday through sunday have been a new flavor of difficult, though i’d take them over waiting on genetic testing results any day. being on estrogen and steroids in combination have really made me moody, angry, irritable, and anxious. taking two doses of estrogen too close to one another one day produced an astounding bought of night sweats. i woke up so drenched that it was disorienting. i experienced that once on clomid as well–no bueno. my tiny peek into menopause.

i’ve tried (pretty successfully) to keep the beast at bay this week with hiking. i’m not supposed to over exert, so i put out a call to my 4000-footer hiking page for flat recommendations, and they did not disappoint. i’ve gone some beautiful new places, and it feels really good to move my body. i feel weight packing on (probably a considerable amount of water retention) despite long stretches of daily movement and pretty impeccable eating, so it feels good to keep my joints moving and my heart pumping. i don’t need or want a small body, but i do need and want a comfortable and capable body.

tomorrow (monday) will be my next monitoring appointment, meaning i’ll go in at the crack of dawn to have (anotherrrrrrr) transvaginal ultrasound and round of blood work to check my uterine lining for goldilocks thickness and my hormone levels for cycle appropriateness.

i’m calling in a normal lining, 9-11mm thick and multilayered, and an embryo transfer date of the following monday.

yours truly,

a hopeful mama

ivf day 32: back to the business

today has felt so much more grounded than the past week, for which i’m thankful. my mental health is much improved, and we’re back in the “doing things” phase again.

today was my first monitoring appointment for what’s called the “fet cycle” portion of ivf. fet stands for “frozen embryo transfer”, and it means that the goal of this phase is not to get my body to produce tons of eggs but to get it to produce a super amazing uterine lining ahead of embryo transfer. at today’s appointment, i had blood drawn for lab work to make sure my body was back at baseline after making ALL THE EGGS (it was) and an ultrasound to make sure my uterine lining had done the same.

the ultrasound showed that my lining was thicker than expected for this point in my cycle. the nurse who i spoke with said this was most likely some incomplete shedding since i’d been put on birth control. i managed to stifle rage over having been told by the previous nurse, in response to the question “will using birth control affect my uterine lining at all?” that no, indeed it would have no effect. a different story from every person you talk to…

side note: one of the downsides to less expensive care is less continuity of care and the constant need that you have to stay on top over everything yourself. sigh.

so we’re going to go forward as planned and see if everything corrects. if it does, we should have a date for our embryo transfer and next trip to new york by next monday after my next set of labs and ultrasound. if not, i have to take (and then abruptly stop) progesterone, have another period, and then start my fet month all over again, including buying more meds. can’t even put my brain there right now. not gonna do it.

for now, it’s meds (estrogen, lovenox injection, aspirin, prenatal vitamins, all the supplements from before, naltrexone, prednisone, and eventually progesterone), trust, and crossed fingers.

onward, little 6AA (for whom we will find a better pet name, i promise)

yours truly,

a hopeful mama

ivf days 30-31: what’s ours

i’ve thought a lot, since announcing that our embryo was euploid, about what belongs just to us, just to stephen and i, throughout this process that’s been so incredibly public. the lead up to this point in our journey has included some parts willingly and purposefully made public: i’ve made a point to share a no-holds-barred accounting of what this is all like so that people can have greater understanding for themselves and a greater empathy for people they know undergoing this wild thing. i did that for clomid months and iui months, and i’ve done it here and on social media for ivf. it’s been a delight and a medicine to write about the good parts and the hard parts, and the engagement i’ve gotten as a result of it feels deeply connecting (a feeling that we’re all lacking in almost-post-covid times, amirite?).

it has also, though, included parts that were public or that were not our own that we’d rather not have needed to include. i’ve paid thousands and thousands of dollars for dozens of invasive and uncomfortable pelvic exams from near strangers each month when i needed more letrozole, clomid, diagnostic testing, or medical procedures. stephen has had to procure semen samples for analysis and fertilization in *office/lobby restrooms* (inexcusable, providers!) rather than in the privacy of our home. i was unconscious when my eggs were harvested (i mean, thankfully), and neither stephen nor i were present when my eggs were fertilized with his sperm. a team of fertility doctors, nurses, anesthesiologists, and embryologists were the only ones present when all of that harvesting and fusion magic happened, and we were left hitting “refresh, refresh, refresh” on the health portal.

we didn’t even get to see images of our embryos until day 7 after fertilization.

in short, every single step of this process has involved an army of people, it’s lacked a great deal of intimacy and personal access, and it has included very, very little privacy.

*******

when we announced that our embryo was euploid, it didn’t take long for folks to figure out that meant that we *also* had details about the 23rd chromosome pair.

XX baby?

XY baby?

and here’s the sitch: no matter how irritating you may find this (and people do), this is the one thing that’s going to be ours. the *one* thing. this is the one tiny piece of surprise and mystery that we’re holding and maintaining, and it’s a thing we’re claiming. it’s not our families’. it’s not our friends’. it’s not our midwives’.

it’s ours.

sorry not sorry ❤

and besides–intersexuality is as common as red hair, and the kiddo will be an ever-evolving and ever self-defining entity until their death day, so those genes are only a starting point anyway. a framework for assignment at birth.

**********

if about right now you find yourself shifting uncomfortably in your seat and thinking “but how will i know what to buy this baby??” i’ll refer you to the hilarious flow chart below for some comic relief:

concept credit: kristen myers. art from sacraparental

seriously though. i hear and honor you if this feels hard, but it’s a decision we feel good about. and it’s also, to be clear, not part of a guarantee yet. our embryo has a 3/5 or 4/5 chance of “sticking”, based on what research you read, so again, there’s no pregnancy yet; no kid yet. it’s our most fervent hope that, sometime before june 2023, you get to meet this little being along with us.

on a related note: we aren’t raising our theoretical baby as a “they/them”, because in my view assuming that as an identity is just as assume-y as assuming “he/him” or “she/her”, (goddess bless the limitations of language!), so if you want to know, you will in something just under 10 months. and if it changes along the way, you’ll know that too as kiddo grows up.

until then, enjoy your turn hitting “refresh, refresh, refresh”. all will be revealed. (shit, i hope so!)

yours truly,

a hopeful mama

ivf day 30: NEWWWWWWWS

i got up this morning to see the hubby off for work, knowing that i’d likely get a call at some point during the day and need to either make or break his day with a text update. noooooooo presha. i had a six-week postpartum home visit with a midwifery client (the last time we see folks after a birth) scheduled for 10am, and i was dreading the possibility of receiving a bad news during the appointment. my last miscarriage necessitated cancelling a day of prenatal visits, and it seemed to unimaginably horrendous to have a repeat trainwreck of midwifery work with personal and bad news, especially since the due dates (through no purpose of mine) would be the same.

i passed the time in the early morning making a new altar filled with embryo-esque sacred geometry: a gilded wasp nest, a hexagon of candles, a fractalled gem brooch. i tucked a little note behind the pin of the brooch that said “euploid 6AA”. i wrote “1:15pm call” on the white board. i packed up all the trinkets and notes and well wishes from others, keeping everything spare.

for today, it’s just me, stephen, and 6AA.

******

i headed out, started and finished my home visit appointment without interruption, picked up my little blister pack of birth control (side note: enskyce sounds less like contraception and more like something you’d do with a surgical instrument), and pointed back towards home.

at 12:53, my phone rang. (not bad with the 1:15 prediction!).

“no caller id available”

that means a nurse.

that means news.

i sat down on the couch, pushed the green answer button, and said hello. my eyes were closed and my hands were shaking. my mouth went immediately and completely dry.

and time stopped.

it must be a little bit like being a 911 dispatch, desperately wishing the rambling person on the other end of the phone would get to the point. YES BUT WHAT IS YOUR EMERGENCY, SIR??

name? confirmed.

date of birth? dear god–confirmed.

statement of “reason i’m calling today”. YES I KNOWWWWWWWuh.

and then an instant flood of tears with the news: 6AA is perfect. euploid. correct number of genes. everything is right. the process continues.

the anticipated/unsurprising “bad news” was that the other embryo, the 4CC, was aneuploid, with trisomies of the 12th and 17th chromosome pairs. incompatible with life and would have been a miscarriage. goddess rest its little cells, and i’m glad to have been spared that experience.

i cried like a baby and laughed with the nurse about how amazing and horrifying her job must be to call people with amazing and horrifying news all day.

congratulations, your embryo is good!

i’m so sorry, your embryo is no good.

back and forth forever.

*********

when i got off the phone i cried more and yelled happy yells, texted stephen who was out on his route, messaged friends and family, and updated folks following along on social media.

6AA is a go. we’re still in the running for success. the biggest (but not the last) hurdle is over. success is between 60 and 80%, depending on what study you ask.

and now, i’m going to go sleep… for a week. birth control for three days to pause things, a monitoring appointment on monday, and onward we go.

yours truly,

a hopeful mama

ivf days 27-29: medieval torture

the last three days have definitely been the hardest on my mental health of this whole endeavor so far. i haven’t experienced so much fog and anxiety since the height of pandemic-work-pivot-nightmare. i no longer have the routine of meds to measure out my days, and i’m not “doing” anything ivf-y besides

just. gruelingly. waiting.

and then there’s the hyper-vigilance. as a midwife, i sometimes feel this creeping in if i’m at a long birth and have a another complicated 42-weeker waiting in the wings: constantly distracted with the idea that the phone might be about to ring, and jumpy. as. hell. when it does. our genetics company runs out of nj, and on day 26, after i wrote the last post, I missed a call from nj and was shaking as I hit redial.

it was our roofer.

my logical brain knows no call until thursday/friday at the earliest, but my lizard brain is READY to know that our 6AA is perfect. I decided the only reasonable response was to hike about it, so i went to white lake state park (picture above!), where one loop turned into three just to pass the time and move my body.

days 28 and 29 were spent with one of my very best pals as he house-sat for friends. we had a fancy dinner, watched the best three episodes of buffy the vampire slayer (hush, the body, and once more with feeling–fight me if you feel differently!), and enjoyed much general laziness. it helped to have something to at least partially take my mind off. the evening of day 29 was spent with a group of pals at a dinner, after our outside city romp was rained out. cny did not, indeed, call.

fill that calendar. quiet that crazy.

tomorrow, day 30, is the second most likely day that we’ll hear from cny with results from cooper genomics, but it could be as late as saturday or monday (cny is closed sunday even though cooper is not–UHG). i realize that my perspective is colored by the fact that this excruciating wait is personal, but it seems unnecessary and unacceptable to have such a wide range of possibility for news. it’s like the cable company saying that they’ll be to your house between 8am and noon, but times a million.

the nightmare: there exists information about whether or not this whole thing continues to be “successful” or has all been uncomfortably and expensively for naught, and we’ll call you at *some undesignated time* during this *four-day span* to tell you.

torture.

i’m not in good shape, but i’m calling myself lucky for having enough generally good mental health to notice an acute, temporary collapse.

perspective and *a thread* of capacity. and a great partner and lot of amazing friends. that’s what’s keeping me hanging on and able to show up both for myself and for a partner enduring the same thing.

the other interesting complication about today, thursday, day 29, is the fact that, since i started my period yesterday, i technically need to have a monitoring appointment at coastal tomorrow morning at 8am if i’m planning to have a frozen embryo transfer this coming month. my choices are 1) book an appointment and risk it being an $800 mistake if i don’t have any viable embryos or 2) take birth control all weekend to “pause” my cycle and pick back up on monday if we get to have an embryo transfer, and risk being turned into a hormone monster, which is my unfond memory of birth control.

my heart wants to chance it, but my bank account can’t afford to be wrong.

so here comes the hormone monster!

yours truly,

a hopeful mama

ivf days 24-26: holding pattern

not a huge amount to update here other than to follow up on how incredibly hard it is to sit with the unknown. our two little embryo biopsies were sent to cooper genomics at the end of last week, and it takes “7-10 days” to get results back. it’s $850 for the two reports (eek!!) and insurance doesn’t even think about covering it. elective. cosmetic. specialty. frivolous. which is wild to think about, since it means me saving myself a likely early miscarriage with potential medical management thereof if we’d blindly implanted an aneuploid embryo. truly, our thoughts around “medical necessity” are bizarre.

in general, waiting means holding a 50/50 chance for the 6AA embryo and < a 25/75 for the 4CC. i’m honestly thinking about it like one embryo with a 50/50 chance since the other seems so unlikely.

tomorrow or the next day (hopefully?) i’ll start my period, which means calling cny and starting the whole cycle of baseline labs and ultrasounds again. after insurance, these trips cost me $500-$800 each (plus gas for 2.5 hours of driving and my time), depending on what labs are needed. i’ll be doing that dance for 14-17 days before we go back to albany for frozen embryo transfer (fet).

i’ve set up my meds station again, and this time around i’ll be taking:

  • estrogen in oral tablets (to build up my uterine lining and make me crazy)
  • progesterone in oil injections (to mature the lining and make my backside look like i frequent a bdsm dungeon)
  • progesterone vaginal suppositories (see above, sans bruises)
  • lovenox injections (a blood thinner to increase the odds of keeping an early pregnancy implanted)
  • claritin tablets (to quiet any histamine reactions from “foreign tissue” being noticed by my body)
  • low-dose naltrexone capsules (a “won’t hurt/might help” anti-inflammatory)
  • intralipids iv weekly until 12 weeks (also won’t hurt/might help, potentially promising for people with a history of early losses, but unclear whether there’s a general benefit)

it’s wild to think that i’ll likely have to start taking these medications before we know if either of the snowseeds are seaworthy. for now, i’m holding absolute trust that one of them absolutely will become a viable pregnancy. i’ll post more updates as soon as we know, which will likely be this coming friday or monday, and because i’ve let so many people in, i will kindly ask that you not contact me for updates. you can send good vibes, yes please! but when we know more, you’ll know more–likely on social media before here.

in the meantime, on to as much distraction as i can comfortably muster!

yours truly,

a hopeful mama

ivf day 23: the weight

when i was 25, i had pertussis, aka whooping cough. i’d been vaccinated against it as a kid, but like most young adults, i’m positive i was AGES behind on boosters. couldn’t tell ya (before then) when the last time i’d had a t-dap was. high school? middle school? anyway, i’d caught it in the petri dish that was the university of alabama, and it was miiiiiiiserable. i didn’t have health insurance at the time (and for a long time i didn’t know how serious my “cough” actually was), so i didn’t go to the doctor. i was in grad school at the time, and i unproductively and uncontrollably coughed my way through research and bibliography, pedagogy, and spenser (sorry, ua english). could. not. stop. choking, tears rolling down my face. low-key always there. i coughed all night every night. sometimes until i dry heaved. i was worried i might break a rib. neither stephen nor i slept well for 5 weeks.

so eventually this situation became so untenable that i made an appointment at the student health center on campus. the discount doc. the place you never want to go. although no longer housed in russell hall, it was still lovingly known by ua long-timers as “russell student death center”. after waiting the requisite 2 hours (coughing the whole time), i was called back and saw the doogie howser on duty that day. he listened to my symptoms, interacting intensely with his charting, and he looked up long enough to ask, “…have you thought about losing some weight?”

he swabbed me (covid-style brain swab) and sent me home with an antibiotic (that eventually helped) and a giant bottle of codeine cough syrup mixed with lidocaine (that wound up going the the trash). no recommendation to quarantine, no instructions to stay away from others… just a crucial reminder that i was basically a walking time bomb of fat. (and had i noticed?)

i start with this story because it’s one with which i and many people are so. very. incredibly. familiar. regardless of consent to conversation, regardless of relevance to the current complaint, fat people (my preferred nomenclature, with deepest respect to the preferences of others) are aaaaaaalways proselytized to by the vague and moralizing cult of “the healthy”.

sidenote props: before i talk any more about life as a fat person, i want to acknowledge that my family absolutely never body shamed, which is apparently quite precious and unusual based on my conversations with other humans. weight was never, ever a marker of worth or something that needed to be changed in my home, for which i am thankful and owe the shred of physical self esteem that i escaped my first two decades clutching (and which subsequently grew into something fine and thriving when adult me dgaf-ed hard at that mess from the rest of the world). i was never weight shamed by my pediatrician, dr. snyder, and my first endocrinologist as a teen, dr. ovale, told me that big thighs and a big rear weren’t poor metabolic health markers. my current np is a dream, as are the folks in my obgyn and fertility practices, but the 20 years of healthcare that i received between those bookends has been a big fat (haha) train wreck.

so, fast-forward to 2021. when we started thinking about ivf treatment, and entertaining the possibility that we could raise enough money to do it (average cost to a live birth in the usa is $34,400.00), i did what any reasonable human would do–i reached out to the local fertility practice here in maine with some questions. i’d learned the power of stating needs, boundaries, and goals for care ahead of time from previous interactions with my obgyn team at coastal women’s health, who without fail remember each time that i decline to be weighed (win!!), so i was proactive with my questions to the local practice.

*i only want to be weighed when it directly and provably impacts medication dosage.

*i decline discussion about bmi, a racist tool developed by mathematicians, not doctors, for the purpose of studying populations, not people.

*i regularly hike 4000 foot mountains and run train for half marathons–i decline “exercise counseling”.

*i have an 80/20 whole foods diet and a deep understanding of nutritional principles (and of the inherent problems of “nutritionism” in western culture)–i decline “nutritional counseling”.

*will this practice accommodate my goals in a shared decision-making model?

their answer: we actually have a bmi “cut-off” over which you will be required to have regular nutritional counseling at additional expense, and your insurance is unlikely to cover you for fertility treatment anyway over that limit (completely untrue, and a scare tactic). there’s also a total bmi cutoff over which you aren’t a candidate for fertility care at all here because it “isn’t safe” (meaning they aren’t trained to manage it). we will weigh you at each visit because we “want you to be healthy and have a healthy pregnancy” (please note, this person does not have my BP, cholesterol, blood glucose, or metabolic panel levels–they’re simply referring to assumed body shape).

this call sent me first into a red rage and second to the next closest clinic in new hampshire for a second opinion. same thing, with a slightly higher bmi cut-off.

fun side note: fertility clinics will often “require” people to lose weight, even going so far as to recommend risky and drastic gastric bypass surgeries that remove whole sections of someone’s digestive system, leading to nutritional deficiencies and relying on starvation and massively disordered eating to achieve what are usually temporary results with lifelong side-effects. even people whose “biological clocks are ticking” have docs suggest wasting 2-3 years of time for surgery, loss, and restabilization before they can be eligible for (read: deserve) fertility care. unacceptable.

the real drives here? moralizing about weight (because we’re really good at that), and keeping clinic success rates high for marketing purposes.

so, you might ask, if fat people have less success with ivf, is the concern legit?

surprise, surprise. it’s complicated.

there are certain metabolic conditions like pcos that both make ivf (and conception in general) more difficult aaaaaaand cause someone to gain weight. “being fat” doesn’t give someone pcos–the syndrome that results in long anovulatory cycles and testosterone dominance also includes differences in insulin sensitivity that cause weight gain, especially in the midsection.

i don’t have pcos. (AND people who do deserve good fertility care)

then there’s hypertension, which can complicate both fertility treatment and pregnancy. fat people are more likely to have hypertension than the general population, but there are medications and lifestyles changes that can address many types of hypertension without the focus being on “weight loss”.

i don’t have hypertension. (AND people who do deserve good fertility care)

then there’s type 2 diabetes, which through a number of factors affects fertility rates and pregnancy health. around 85% of people with type 2 diabetes have what the us medical system considers a problematic/unhealthy weight.

i don’t have type 2 diabetes. (AND people who do deserve good fertility care)

so where does that leave us “fatties without comorbidities”–the people who inhabit societally unacceptably large bodies but who don’t have other markers associated with “lack of health”? and how can we continue conversations that unquestionably include and center the experiences and needs of people who do have other comorbidities. i don’t get a prize for being a “healthy fatty”–i’m a human deserving of healthcare like every. other. human. here.

but for the sake of thorough exploration, what, if not blood pressure, glucose, and metabolic disorder would give large-bodied folks poorer fertility outcomes? let’s consider…

*fat people are less likely to seek preventative care like regular check ups and cancer screenings

*fat people are more likely to have poor/distrusting relationships with medical providers because of both overt and subtle expression of provider bias (or even disgust) over a lifetime

*fat people are less likely to be believed when they report food intake, body movement, and lifestyle factors

*fat people are often 5-10 years behind their thin counterparts in disease diagnosis because all symptoms are so often attributed to/blamed on their weight

*fat people don’t have access to the critical care they need without jumping through moralized hoops around “needing to lose weight” before having access to care

*fat people encounter a lack of appropriate medical equipment when needed (bp cuffs that are too small will read abnormally high, needles that are too short might not get medicines into muscle tissue, etc.)

*fat people have increased rates of anxiety and depression related to the consumption of medical care because episodes of care so often contain shaming, even when weight is not the focus of a visit

*provision of care is often preceded, out of provider-espoused necessity, by massively disordered eating in an attempt to lose weight (which both causes an inflammatory state in the body and fails to result in lasting change over 95% of the time)

i could go on and on and on.

just “being fat” is not a risk factor. being “treated like a fat person” though absolutely is.

side note: it’s not at all the same thing, but on a related note, i always tried to train my students to replace “the lifelong experience of systemic racism” when they read “african american” or “black” as a risk factor. 99 times out of 100, that’s really what the data reflects. similar situation here. occasionally, being fat causes problems. often, problems cause being fat. always, reception as a fat person explodes the whole situation.

***************

i feel like this has been a really winding but important deep-dive rationale for why, in addition to cost, we ultimately chose cny for our fertility care. i knew after my first couple of local phone conversations that care with either of these two local places was going to feel bad. what i was looking for was scientific assistance with fertility, and what they were going to provide was morality based, evidence-scarce pressure to change myself. instead of relaxing and focusing on ivf, i’d be stressing and straining to lose weight and needing to “prove it” at weigh-ins. fuuuuuuuuck that.

and you know? i’ve done that. i weighed 260 when stephen and i were first together. didn’t get pregnant. i lost 80 pounds before our wedding. didn’t get pregnant. i crept back up to 275 in the seven years following. GOT PREGNANT. i lost 75 pounds. GOT PREGNANT. i lost 45 more pounds. didn’t get pregnant. my weight, she ain’t the problem.

in my first phone call with cny, which was with the nurse practitioner overseeing my care plan ahead of egg retrieval, she actually didn’t mention my weight at all. given my history with healthcare providers, this was so uneasy to me that i actually brought it up.

me: “do you think my weight will affect my chances and my care?”

her: *looks at chart* “oh gosh no, i don’t think so. not at all”

me: “do you require nutritional counseling?”

her: “does that feel important to you or like it would be helpful?”

me: “no, i’m a midwife and a health-minded person with decent access to resources, so i’m good”

her: “then absolutely no, not unless that’s a goal for you”

(ensuing conversation about the toxic nature of medical fatphobia)

in the entirety of my care at cny, i self-reported weight once on an intake form, and last week the nurse asked me to “just grab a quick weight before surgery so the anesthesiologist would know how much propofol to give me”. that’s it. no moralizing. no gatekeeping. no patronizing. no shaming. data gathering when data was needed. and there’s plenty of information available through the practice about eating for health and fertility, but it’s all simply available on offer, not a required regimen or forced discussion.

game changer.

and cny does this at professional cost, though it doesn’t seem to be hurting them. they take people regardless of age and regardless of weight (both of which are definitely not the norm) with the full understanding that this will make “their numbers” not their selling point. their philosophy is affordable, personalized, informed care for all, and i am delighted to report that it’s been a life-changing experience for me.

it’s a tender and vulnerable thing, but i invite you to share your stories, in the comments below, of times you received very poor or very exceptional care in a body that deviates from our narrow views of healthy. what was the experience like? how did it affect you? has it changed the way you advocate for yourself?

thank you in advance for your your candor and vulnerability in sharing experiences.

yours truly,

a hopeful (fat, and healthy) mama

ivf day 22: relentless attrition

while i was out on a hike today, i received quite a mixed bag of news from cny. the adventure continues!

(from left to right:)

embryo #1: while yesterday was indeed listed as the “biopsy and freeze day” in my health portal, only two of our sweet three stayed viable long enough for that to happen. our third little amigo, who was neither biopsied nor frozen, got to spend 6 rad days as a never-before-seen-in-this-reality genetic combination, and the universe got to experience itself as that little embryo for almost a week. it’s really kind of mind-blowing to think about. so long, little comrade, and may your cells go to good use and bless and enrich scientific discovery.

embryo #2: one of the two embryos that was biopsied and frozen received the lowest possible score from embryology, a “4CC” meaning it was behind in development and showed a low quantity of cells both in the trophoblast (the outer “beachball”) and the endoderm (the inside clump that will eventually become the fetus). this isn’t the end of the line for #2 quite yet, but it means a much larger likelihood that there’s a genetic issue. we’ll know that hopefully by the end of next week. also of note: embryo grading is incredibly subjective and not the final word on anything, but we’re prepping for #2 to be a loss.

embryo #3: lucky #3 received the highest possible grade for an embryo, 6AA, meaning it has already successfully “hatched” from its blastocyst shell called the “zone pelucida” (latin for “see-through girdle” HA!) and it shows a large and thriving quantity of cells both in the trophoblast and the endoderm. in the picture above, it’s the one that’s YUGE AND PERFECT. first school picture. it’s going on the fridge. but really though, the game changer here is that, although embryo grading is more art than science, one study found that 6AA embryos had a 65% pregnancy rate and a 50% live birth rate. that’s up from the 14% general statistic for random eggs at my age. no guarantees with a 6AA, but our odds of success just went up despite losing one and probably another. if the testing for #3 comes back normal (we’ll know in just over a week), our odds go up to 85% for a pregnancy that progresses to at least 24 weeks (that study didn’t include life birth rates. rude.)

all of this is technical data. labs. grading. odds. it’s worth noting though that none of this feels technical in my or stephen’s hearts and minds. this is all exciting and excruciating. it’s cringe and brace and hooray and crickets and tears and magic and horror. i’m amazed at what our bodies were able to do in marriage with science, and i’m devastated every time that number ticks down. i’m terrified of it hitting zero, and i know it won’t, but i worry that it will, and i know that it won’t–back and forth forever.

each piece of news from me is a text message that might make or totally derail stephen’s day. will it be yay! or will he need to drop everything and come home? how do you grieve at and with a person who is grieving for the same reason? how do you stay in a place of both hopeful joy and realistic authenticity in knowing the odds?

this experience has been all-consuming for me. i don’t have bandwidth for anything else or anyone else. i don’t answer emails. i’ve cancelled meetings. i don’t give two shits (temporarily, and not in a bad or scary way) about ordinary life things. i’m getting out for walks and hikes to pass time, but i have zero capacity for responsibility. i feel like it’s taking all i have to hold this…

…and i’ve drawn so much energy and stamina from all of you standing alongside us. thank you for being here for the joy and the horror that is in vitro fertilization.

yours truly,

a hopeful mama

ivf day 21: genetics

so we got the AMAZINGLY GOOD news yesterday that all three embryos made it to blastocyst phase, meaning they were happy in the lab and grew from single cells to mulberry-ish clumps of cells to big hollow fluid-filled beachballs. the outer ring of the beachball, the “trophoblast” (greek: “immature cells for feeding”) will eventually become the placenta that “feeds” the embryo/fetus, and inside the trophoblast layer, there’s a clump of cells off to one side called the “endoderm” (greek: “inside skin”–kinda creepy) that will eventually become an embryo (2-8 weeks after conception) and then a fetus (8 weeks from conception to birth). the clump will differentiate into three separate cell layers (think a stack of pancakes), then roll up into a tube (think an enchilada made of 3 pancakes), then curl into the classic embryo shape (think a macaroni noodle made of a 3-pancake enchilada). that’s you and me. we’re glorified macaroni noodles. just tubes with attitude.

this morning, at 6 days of age, our embryos were biopsied (a couple of cells were pinched off the trophoblast–not as risky as it sounds) and then sent into cryostorage. they’ll stay frozen on day 6 of development until we thaw them for transfer, and in the mean time, those three sets of cell samples are being sent to a lab for genetic testing. lots of folks have asked me about that, so i figured i’d expound a little in today’s post. stay with me 🙂

genetic testing isn’t “choosing eye color and hair color” and all of the things that we associate with high school learning about expression of dominant and recessive genes. each of the samples we sent will undergo karyotype testing for what are called “aneuploides” meaning too many or too few chromosomes. these errors can occur during meiosis (the cell division that produces eggs and sperm) or mitosis (the cell division that happens after fertilization).

at my age (40), there’s a whopping 86% chance that any given egg will contain a genetic error caused during meiosis. if you think waaaaaaay back to your last a&p class (which was likely high school bio), you’ll remember that during cell replication, the soupy, unorganized chromatin in a cell’s nucleus organizes itself into the “chromosome shape” that we think of when we think of genes, does some replicating and some gene swapping, and then spindle fibers pull the chromosomes to their own side of the cell before cleavage and division happen (massively simplified–here’s a good image of meiosis). as XX folks age, our spindle fibers get tired (a lifetime of paying taxes and fixing everyone else’s problems will do that, y’all), and they may pull all the genes to one side before division, creating one cell with too few genes and one with too many.

so lets say you have an egg with too many or too few genes, and it combines with a sperm that has its own set (23 chromosomes, or half a hooman). if your egg has an extra copy of one of the chromosomes, you wind up with one of the “x shaped” chromosome pairs that now has three sets (looks like XI) instead of two (looks like X). this is called a “trisomy” (greek for “three bodies”). most trisomies are not compatible with life, meaning cell division will arrest at some point or that an embryo, fetus, baby, or child will die as a result. a few trisomies are compatible with life: trisomy 21 (three copies of the 21st chromosome, or down syndrome) and sex chromosome trisomies (shout out to my XXX friends!) are examples.

if the egg with too few chromosomes is fertilized, it results in what is known as a “monosomy” (greek for “one body”, and on a karyotype you’d see the “I” of one set of genetic information where you’d expect to see the “X” of two sets. only one type of monosomy is compatible with life, and that’s monosomy at the 23rd pair, or XO sex chromosomes (X nada, compared to XX, or XY). this monosomy is called turner syndrome, and while compatible with life, it causes short stature, infertility, and often heart and other organ system problems. actress linda hunt has turner syndrome, for stature reference.

all of this to say that because my old-ass spindle fibers aren’t so much interested in reproduction this late in life, only 1 in 7 eggs that i produce will be free of trisomies and monosomies. that’s 14%, y’all. sperm are much less likely to contain these errors because they’re batch-made fresh daily (sorry), but it is possible. it’s also possible that egg and sperm are fine that but a trisomy or monosomy is caused early in mitosis after fertilization, and that error replicates in a way that will eventually cause arrested development of an embryo or a situation incompatible with life for a fetus or baby.

fun fact: these errors can also produce “mosaic” embryos that are a combination of normal (“euploid”) and abnormal (“aneuploid”) cells, and embryos can sometimes correct this error and junk the bad cells!

our genetic testing, then, isn’t about eye color. it isn’t about intelligence, handedness, or ability to curl a tongue. what cooper genomics will be looking for in our wee three will be complete sets of chromosomes. question: are all of the instructions to make a human there with nothing missing and no competing copies? 46 chromosomes in 23 pairs. goldilocks style–too many? too few? just right? when we get our report back in nine days (DID I MENTION WE HAVE TO WAIT NIIIIIIINE DAYS?), we’ll know whether any/some/all of our embryos are genetically viable. each has a 14% chance, which seems abysmal, but i keep reminding myself that stats like this only really matter on a population scale. they could all be perfect and normal. i’m voting for that one.

fun side note: because the 23rd set of chromosomes tells us XX or XY, we’ll know the assigned sex of our embryos. even cooler: there still gets to by mystery because we won’t know how they would grow up, look, develop, express, be, feel, and identify. even weirder: if all are viable and there’s variety, we can choose an XX or XY kid. even meaner: if we do, we aren’t going to tell anyone! mwahahaha.

so that’s where we are today. the snowseeds are on ice, samples are en route, and scientists will be doing scientist shit with them over the next week.

folks, if we clear this hurdle, even with one of the embryos, there’s almost an 85% chance that embryo transfer will result in a viable pregnancy. each hurdle has felt enormous, and this one feels biggest of all. thanks for being along for the ride!

yours truly,

a hopeful mama