Showing posts with label stress. Show all posts
Showing posts with label stress. Show all posts

Sunday, November 10, 2019

Diabetes & Pregnancy: The 2nd Trimester

For my account of managing my diabetes during my first trimester (0-13 weeks of pregnancy), visit this blog post.

*Disclaimer: These posts are not meant to give medical advice. I'm not a doctor. I'm merely recounting my personal experience managing Type 1/LADA during my pregnancy - and everyone's diabetes and everyone's pregnancy is different.

**

I started out the 2nd trimester (14-28 weeks pregnant) with an incredible A1C of 5.1% - likely due, at least in part, to how many low blood sugars I was having at the end of my 1st trimester. Around 14-15 weeks pregnant, I was taking 18 total units of insulin a day: 6 u. of Levemir (my basal insulin) in the morning + 4 u. at bedtime, and 2 u. mealtime insulin with breakfast, 3 u. with lunch, and 3 u. with dinner. This was probably too much, and the beginning of my 2nd trimester still saw several instances hypoglycemia. Even with blood sugars lower than 55, I rarely felt symptoms. If I felt anything, it was only being a bit warm, or feeling irritation at how difficult it was for me to poke a straw into a juice box. Thankfully, my CGM (continuous glucose monitor) continued to be pretty accurate, now that I was wearing it on my arm rather than on my abdomen, and I could (usually) count on it to alert me when I was going low.

Also thankfully, most of my low sugars were now happening during the day instead of overnight. I didn't mind these as much - they were typically 2-4 hours after eating a meal or snack, and about when I would/should be eating another meal or snack anyway. I was also more likely to notice falling blood sugar before it got low enough to trigger the urgent low alert on my CGM, since I was awake and looked at my CGM often. If I saw I was at 72 and still trending downward, I could just adjust when I planned to eat next, or how many carbs I planned to eat, to avoid having to treat with candy or juice.

Still, just because daytime hypoglycemia is easier to deal with doesn't mean it wasn't a nuisance at times - like around 16 weeks, when I saw blood sugars below 65 six times, sometimes more than once in a single day. At 16w3d, I had blood sugar that stayed stubbornly in the 50s-60s for nearly three hours, despite eating candy, yogurt, pasta, and more candy. And the next day, my CGM urgent low alert went off another three times: once overnight (at 4:30 am), once three hours after breakfast (at 10:30 am), and once 1.5 hours after dinner (at 7:30 pm). These were not particularly unbalanced meals either, that might have caused a post-meal sugar crash. I tried not only to eat the recommended 50-60 g. of carbs with every meal, but also to balance those with protein, fiber, and fats.

Like I had done before in the 1st trimester, I started decreasing my mealtime insulin doses without express permission from my doctors, making small adjustments as I needed to in order to get through the day. If I was already below 70 before eating a meal, for example, I might take only 2 u. of insulin with my meal instead of 3 u. But even those adjustments weren't always enough, and MFM (maternal fetal medicine, the doctors and nurses who were helping me manage my blood sugar while pregnant) suggested I decrease my morning Levemir by one unit. A week later (at 17 weeks), they extended that suggestion to my nighttime Levemir as well. For the next several weeks, I took 5 u. in the morning and 3 u. at night. Even with those changes, I still had to occasionally take only 2 u. with lunch or dinner; on such days, my total insulin was therefore down to only 15 u.

During the four weeks from 17-20 weeks pregnant, I had blood sugars under 65 twelve times, for an average of three times a week. However, around 19.5 weeks, something else started to happen - even though I was still having occasional daytime lows, I was also having some daytime highs as well. I saw numbers in the 140s-150s more regularly after breakfast, and occasional blood sugars in the 140s or even as high as 180 after dinner. For a non-pregnant diabetic, those numbers would still be considered pretty good, but pregnancy blood sugar targets are <120 two hours after eating, so at the end of 20 weeks, MFM recommended I increase my breakfast insulin to 3 u. This helped, and between 21 and 22 weeks, I had fewer instances of higher glucose - but even more instances of low blood sugar. During those 2 weeks, there were 8 days when my blood sugar dipped below 65.

20 weeks marks the halfway point of a full-term pregnancy, and about when most pregnant people have their "anatomy scan" to make sure all the organs look normal and the baby is growing appropriately. Because of my diabetes, I was also given a fetal echocardiogram - a more detailed look at the baby's heart, to make sure it was pumping and working as intended, and that all chambers and major vessels were accounted for. My anatomy scan and fetal echo were at 21w2d, so that my husband could also be there.


A sonogram from my anatomy scan on September 3, 2019, when I was 21w2d pregnant.

Everything looked great - it was all good news! But that didn't stop me from starting to worry about what my baby's birth weight might be. One of the most well-known risks of a diabetic pregnancy is the risk of a "big baby," and even though I was trying my best to keep my blood sugar levels on target, there were certainly times (an hour here or there, while I waited for an insulin dose to catch up) when my baby was floating in an amniotic sac with high blood sugar. I would sometimes watch my CGM rise near or above 200 after eating - and even though by two hours after eating the number would be back on target (<120), and MFM only cared about that "two hours after" number, I still worried what that half-hour of high blood sugar might've done, before my mealtime insulin kicked in.

I actually had 3 ultrasounds during my 2nd trimester, and the first was at 16w2d, which showed my baby in the 64th percentile for size/weight. I also saw MFM at 17w4d, and my OB at 20w2d, for general check-ins without ultrasounds. They measured my fundal height for the first time at that 20-week appointment. This is a measurement of how high the top of the uterus is, which apparently correlates in cm to how many weeks along one's pregnancy is. I measured 23 cm - a little larger than expected for 20 weeks. Then at my anatomy scan ultrasound at 21w2d, my baby was measuring in the 85th percentile.

I was also starting to gain weight myself, at a rate of about one pound a week. Even though this is the recommended rate for the 2nd and 3rd trimesters, I worried that it was too much, and I would soon outpace this recommendation. I was averaging 2300-2400 calories a day - which was more than I wanted to eat, but when I was trying to make sure I was eating enough carbs and trying to avoid low blood sugars by balancing those carbs with proteins and fats, that amount of calories felt rather inevitable. (Weeks when I had several days of hypoglycemia saw that average raise even higher, to about 2600 calories/day, as I treated my low blood sugars with candy and snacks.)

My doctors, however, were miraculously not worried - not about my weight gain, and not about my baby's size (at least - not yet). They told me babies grow at different rates and it was still too early to tell if it would be a big baby at birth. I was surprised; I'd heard so many stories about doctors' concerns about the size of babies born to diabetics that I was sure that the "85th percentile" news would prompt lectures about dietary changes or insulin adjustments. Instead, they told me I was doing a good job with my blood sugars and that (barring any other complications), there would likely be no need to induce me before 39 weeks after all. (Originally, they'd told me most diabetics need to be induced between 37-38 weeks). They congratulated me on my blood sugar logs and gave me high-fives.

Then, at 23 weeks, the insulin resistance I'd been warned about finally started to hit. That week, I had zero instances of hypoglycemia under 65. It was the first time that I'd had an entire week without low blood sugar in 14 weeks - since my first appointment with MFM at 8.5 weeks pregnant, when I'd started taking mealtime insulin. More than that, I also saw several higher numbers after eating again: 130s after breakfast, 130s (and even a 161) after lunch, 130s-150s after dinner. Most were only slightly higher (and the 161 was because I'd forgotten to take my insulin at lunch that day), but then at the end of 23 weeks I finally saw a post-meal reading that truly gutted me: 208 two hours after dinner. Before when I'd seen a number that high, it had corrected itself before the two hour mark. Or it was high only on my CGM, and a check with my meter reassured me that my CGM was inaccurate and I wasn't actually that high after all. But this time, it was my meter that showed me at 208 - my CGM was inaccurate in the opposite direction, and thought I was only at 174.

Logically, I knew that one night with blood sugar above 200 wasn't going to hurt. It's not about perfection 100% of the time; it's the pattern of your readings and how often the baby (and your own body) is subject to high blood sugars that truly affects health complications. Still, seeing that number dashed my hopes that maybe having LADA instead of a "true" Type 1 meant I wouldn't see much insulin resistance after all. LADA probably delayed the insulin resistance a bit (the book Pregnancy with Type 1 Diabetes by Ginger Vieira warned that insulin resistance might begin around 16 weeks, which I'd passed 7 weeks earlier) - but in the end, diabetes is still diabetes, and even if my pancreas isn't as malfunctioning as others', it's still not functioning as it should be. It's easy for me to forget that sometimes.

In the last 5 weeks of my 2nd trimester, MFM increased my morning Levemir from 5 u. to 6 u. to 8 u., and my bedtime Levemir from 3 u. to 4 u. to 6 u. (and then, when 6 u. proved a bit too high, back down to 5 u.). My mealtime doses were also tweaked - my breakfast Novolog went from 3 u. to 4 u. to 5 u., lunch went from 3 u. down to 2 u., and dinner went from 3 u. to 4 u. With small adjustments being made nearly every week (or even multiple times a week), it started getting very difficult to keep track of what I was supposed to be taking when.

To put another way, I was taking a total of 17 u. of insulin each day at the start of 23 weeks, and a total of 25 u. of insulin by the end of 27 weeks. This was increased gradually at first - I was steady at 19 u. for two and a half weeks, for instance - but then at 26 weeks, MFM started adding more insulin in greater jumps. I had a week with fasting blood sugars consistently between 90-110 (when they're supposed to be under 90), and after that MFM just started piling on the changes (or so it felt to me).

In the past, they usually adjusted me by 1 unit at a time, and then waited a week or so to see if that would be enough - but on October 8 they had me increase my morning Levemir from 6 u. to 8 u., and on October 10, only two days later, they also asked me to increase my bedtime Levemir from 4 u. to 6 u. It solved my high fasting blood sugars (at 27 weeks I was back down to between 70-82 every day), but it also, unsurprisingly, caused a resurgence of hypoglycemia issues. I had 5 days of low blood sugar in the last two weeks of my 2nd trimester, and on the very last day, my CGM urgent low alert went off overnight (twice!) for the first time in 8 weeks. I had to treat hypoglycemia at 1 am - and again at 5 am - and then for the rest of the morning, I continued to struggle getting my blood sugars to stay up. At 7:30 am, before breakfast, I was at 61; by 10:30 am I was back down to 72 and having to eat a snack; and less than two hours later, I was at 62, requiring me to eat an early lunch. After that day, I convinced MFM to back down a little, scaling my bedtime Levemir back to 5 u.

On the plus side, I was able to eat fewer calories most days (those hypoglycemic days notwithstanding), now that I had more insulin resistance. For a few weeks, I was gloriously not worried about low blood sugars at all. My daily calories averaged between 2100-2200 from 23-27 weeks - which was not only more in line with how hungry I was/how much I actually wanted to eat, but also slowed down my weight gain a bit (and which I hoped might also help prevent my bigger-than-average baby from getting any bigger). Still, by the end of the 2nd trimester, I'd already gained 23 lbs. compared to my pre-pregnancy weight - and I had the entire 3rd trimester still to go.

At 24w2d I had another check-in with my OB. This time, my fundal height measured 24 cm - right on track to where I "should" be for how far along I was. For a few days, I worried less... But then at my third 2nd trimester ultrasound at 25w1d, my baby's estimated size/weight came back as being in the 92nd percentile, and all my anxieties and guilt about having a "big baby" resurfaced.

To be clear, I'm not trying to fat shame here. I have nothing against "big babies" in general. I wasn't even that concerned about the idea of having to deliver a larger-than-average baby, which is probably what most pregnant people are worried about when their baby is measuring large. It was just that I was worried I was responsible for making my baby bigger than they otherwise would be, due to the unavoidable fact of my diabetes. If I hadn't been diabetic, I wouldn't have thought much of it - I would've chalked up my baby's size to genetics or something, and looked forward to seeing all those cute rolls on my baby's arms and legs. But because of my diabetes, I was filled with mommy guilt that my baby's size was my fault. I worried I was giving my baby a difficult start to life, and a childhood potentially riddled with health problems, all because of the glucose they'd been exposed to in utero.

That same day I had my A1C tested for the first time since the end of the 1st trimester. Given how big my baby was measuring, how much weight it felt like I'd gained, and my recent insulin resistance, I thought it might be higher than my previous 5.1% result - but hopefully not too much higher. (After all, I was trying so hard to control everything and keep my blood sugars as low as was safely possible for me to do!)... So imagine my surprise when the result came back as 4.8%! All those hypoglycemic episodes had outweighed the few 200+ blood sugars I'd had after all, and my average blood sugars remained solidly in the standard non-diabetic range of 4.0-5.6%. It confused me, frankly. With an A1C like that, what more could I do than what I was already doing? And how could my baby's size be because of my diabetes? Maybe I wasn't at fault after all!

I had another ultrasound at the very beginning of my 3rd trimester (28w1d), which showed my baby now in the 96th percentile.

A 3D sonogram of my baby's face, from my ultrasound at 28w1d pregnant - the very beginning of my 3rd trimester.

My doctors seemed divided in opinion. On the one hand, they still congratulated me on my (mostly) excellent blood sugars (though they also seemed a bit more keen to point out the couple of times I'd gone high); on the other hand, they were non-committal about if my diabetes was influencing the size of my baby. One told me, "Whether it's because of your diabetes or not, making changes to your insulin probably won't make it better at this point. You're just going to have a big baby."

They also started talking about the possibility of an induction earlier than 39 weeks again, and how I wouldn't be able to manage my own diabetes during labor and delivery - I would have to be on an insulin drip so the doctors could control my blood sugars themselves. When I started to question whether I would really need to cede all control over my insulin to doctors who didn't even know me or my diabetes, I was told that if I wasn't on an insulin drip it would make the doctors "irritated" and "uncomfortable." As if my priority when I'm in the middle of childbirth should be being a model patient and doing whatever they tell me, instead of advocating for what I want and need based on what I know of my body and my diabetes. Uh, NO. I don't think so. If that's the person they're expecting me to be, they're about five years too late.

In fact, here's how much I'm NOT that person anymore: about halfway through my 2nd trimester, I decided to hire a doula - a childbirth coach/companion. I worried that doctors and nurses would see the word "diabetes" on my chart, make assumptions about my risk factors, and then make decision about how my labor and delivery would go based on those assumptions, without consulting me first. There were a lot of things I was concerned about - whether or not I'd be induced or require a c-section, whether I'd be allowed to move around or if I'd be connected to too many wires and machines (IVs, fetal monitors, etc.) to leave a hospital bed, and how much I would be allowed to manage my diabetes while in the hospital. I worried that if I was given insulin through an IV, I'd be given way more than I needed, and/or that if hospital staff were in charge of treating any hypoglycemia episodes that may occur, they would over-treat me and make my blood sugar skyrocket (like they did after my D&C last year, when the post-op nurse saw that my blood sugar was slightly below 70 and gave me a huge cup of apple juice to drink, which resulted in me having to deal with 300+ blood sugars for the rest of the day after I was discharged).

I knew I would feel more comfortable with someone in the room (besides my husband) who will help me advocate for myself, ask the questions I want to ask, make sure doctors explain their recommendations to me and keep lines of communication open, remind me what my options are, and emotionally support me through the whole process - whether I end up having a relatively normal labor and delivery, an emergency c-section, or somewhere in between. Based on several articles and books I read, it seemed like a doula was exactly what I wanted - and now that I'm already getting pushback from doctors when I bring up my preferences for and concerns about labor and delivery, I'm so happy that I made this decision to have a doula on my team.

In the end, I realize I probably won't have much of a choice on the insulin IV during labor and delivery - but if I agree to it, it won't be because it's what will make the doctors comfortable; it'll be because it's what makes me comfortable. My priorities are figuring out what's best for myself and for my baby - not what's best for my doctors. For them this is their day to day job; for me, it's an experience of a lifetime, one of the most important days of my life, which I'll remember forever. And when I look back on this experience, I want to remember feeling empowered - not coerced into medical procedures or protocols I wasn't comfortable with and didn't need to do.

There's one last thing I want to talk about regarding my diabetes during this trimester - and that's to talk about the effort it takes to manage a chronic illness. I did already explain this in my last post about diabetes, but I don't complain often (except in blog posts I create specifically to complain, like this one), so please bear with me if I repeat myself a bit. :)

Near the beginning of my 2nd trimester, I switched from using Fiasp brand mealtime insulin (the last of the free sample pens my endocrinologist gave me before I was pregnant) to Novolog (the brand my insurance covered with my new mealtime insulin prescription, which now cost me $40/month). I also got a prescription for meter test strips for the first time; before I was pregnant I was not going through my insurance for test strips at all, and was simply buying them on Amazon. Without a prescription, I was using the Contour Next glucose meter, and paying $34 for 100 strips. With a prescription, I switched to True Metrix (the brand covered by my insurance), and ended up paying only about $4 for 150 strips.

Obviously I was glad to save some money (especially now that I was paying for mealtime insulin)... but those savings didn't come without a price. Getting my test strips through the hospital has proven to be a much greater hassle than just placing an Amazon order. First, I had to pick them up in person because my signature wasn't yet in the system for them to auto-bill my insurance. I was assured it would be smoother in the future, and that next month I could just call, ask for a reorder, and they'd be shipped directly to my house. But by the next month the hospital's medical supply distribution center had changed hands (and names), requiring all prescriptions to be resubmitted. This resulted in three back-and-forth phone calls before I was able to relay this message to my doctor's office and get this problem solved, and then another few days before the request went through, by which time I was down to my last couple of test strips. (Good thing I have a CGM as a backup way of checking my blood sugars!)

And the third month I went to reorder supplies? I had to go through the whole process of resubmitting my prescription again, because somehow they had "no record" of my prescription ever being resubmitted the previous month - or the package of test strips they'd sent me. Then, when that third month's supply finally arrived, it was the completely wrong thing. Instead of getting True Metrix test strips, I was sent AccuCheck lancets (which aren't even lancets I can use, because they require an AccuCheck brand lancing device which I don't have). I had to call them back (again) and ask them to send the test strips I needed.

Refilling my insulin is also often a chore, this time requiring arguments with my insurance. For much of the 2nd trimester I was not taking enough Novolog every day to finish an entire insulin pen before it expired (which, due to the nature of insulin, is 4 weeks after the pen is removed from the refrigerator and used for the first time). This meant that my insurance wouldn't let me refill my prescription when I needed to, since according to them I "hadn't used up" my last refill yet. I had to argue that it didn't matter how much of the pen I used - if I was following the instructions from the medicine's manufacturer, I would need a new pen every 4 weeks regardless. (And I had to make this same argument every 4 weeks, because the solution was always just a one-time override, and not changing whatever needed to be changed so that it wouldn't happen again.)

During my 2nd trimester, I really started to notice how much time and energy I was putting into managing my diabetes every day - and how much harder it was to keep track of everything for so long. I spend a lot of time:
  1. Keeping track of what my blood sugar is doing (both on my CGM and verifying the CGM's accuracy with at least a few follow-up finger sticks a day)
  2. Being constantly vigilant about when I need to eat next and what I should eat next - which also entails deciding whether or not I need to pack a snack and/or insulin pen(s) in my bag every time I leave the house; planning meals and buying groceries up to a week in advance; calculating the calories, carbs, and fiber of every ingredient in every dish I prepare; looking up those same nutrition facts online for any restaurant I'm planning to go to, so I can decide ahead of time what to order; and making a note of those three stats for every bite I put into my mouth
  3. Reorganizing all those pen-and-paper notes I keep into an online spreadsheet so that the info is easier to assess and find patterns, downloading CGM data to my computer from my receiver unit, and printing out all my charts and graphs to take to every doctor's appointment
  4. Remembering what my current dose of insulin is and making sure I take the right amount from the right pen, for 5 different injections taken at 4 different times every day (and properly disposing of my medical sharps, taking them to an appropriate recycling facility when the containers get full)
  5. Dealing with hypoglycemia alerts, sometimes multiple times a day and/or in the middle of the night, having to figure out each time if it's a false alert or real, and (if real) making sure I treat the low blood sugar as required, even if I don't want to - including trying to prick my finger and line up a drop of blood onto a small test strip in a dark bedroom in the middle of the night, or eating a snack when I'm not hungry, and
  6. Reordering test strips and lancets from the aforementioned dysfunctional hospital medical supply center, refilling prescriptions for insulin pen needles and two different types of insulin at Walgreen's, and reordering CGM sensors, transmitters, and overlay patches from another medical supply company, or from Dexcom directly, as needed.
All of that management requires a lot of physical space (our kitchen table is covered in my diabetes notes, paperwork, and prescriptions) and mental space - and sometimes it takes a toll on me emotionally. When I make a mistake (and with that many things to constantly keep track of, mistakes are inevitable), I feel guilty. By 23 weeks (before my craziest insulin adjustments even started), I was already seeing proof that managing every aspect of my diabetes was taking its toll on me. Things that should've been easy to remember started falling through the cracks.

As mentioned briefly above, I forgot to take a lunchtime insulin dose at 23 weeks pregnant, resulting in a post-meal blood sugar of 160 (which I actually thought was pretty good, considering I'd taken 3 less units of mealtime insulin than I should have). Then, a few days later, I finished a box of insulin needles and went to grab a new box off my shelf - only to find that there wasn't one. I'd been so sure I had another box in reserve that I hadn't bothered to check once I noticed the box I was using was getting low - but somehow 40 days had passed since I'd last filled my needle prescription and I'd gone through all 200 needles. This discovery resulted in a frantic phone call to Walgreen's, checking ALL the Walgreen's in the area, and ultimately having to get a different brand of needles than usual (a brand I disliked, because I found that I was more likely to bleed and bruise when using them), which I picked up just minutes before the pharmacy closed (because of course this happened on a Sunday when the pharmacy closed early). I was very lucky that I ended up not having to miss a single insulin dose due to my error; if I'd had to wait until Monday morning to pick up the prescription, I would've missed at least 4 doses, for a total of 16 units of insulin. I had no idea how badly that might have messed up my blood sugars, and was glad I didn't have to find out.

(Though, can we take a moment to please note the ridiculousness of the situation? I HAD medication on hand, just not the conduit to get the medication into my body. I think when you pick up your month's supply of insulin they should include the needles with it, instead of requiring two different prescriptions. Or, you know - maybe not require a prescription for those tiny insulin pen needles in the first place, but just have them available over the counter, on the shelf next to the test strips and lancets... But I digress.)

That was just one small mistake (and one I could easily blame on "pregnancy brain"), but it could've had serious consequences. I had another such mistake after my insulin doses started frequently changing after 23 weeks - I was looking at my evening Levemir dose (6 u.) instead of my morning Novolog dose (5 u.) in my notes and ended up giving myself 6 u. of Novolog instead of only 5 u. Again, in the scheme of things, this wasn't a disaster - but only by sheer luck. I happened, completely by chance, to almost do the right thing, and the difference of 1 unit didn't affect my blood sugars much. But what if I'd grabbed the wrong pen too, and given myself 6 u. of Levemir instead of 5 u. of Novolog? I would've had significantly more basal insulin in my body than I needed, and would've fought dangerously low blood sugars all day long, likely requiring a trip to the hospital to bring them back up.

I know that these sorts of mistakes are inevitable. I try my best to be diligent, but it's just impossible to be completely aware of everything I'm doing all the time. Still, when they happen, it's hard not to blame myself and feel guilty. Even when I don't make a mistake at all, but simply follow the plan my doctors and I have developed, things still happen - things that I want to believe I have control over, but which I probably (for whatever reason) just don't. Despite trying to eat right and get my insulin doses right, that first 200+ blood sugar two hours after eating wasn't the only one I had this trimester (there were two others, too). And despite my 4.8% A1C, my baby is measuring in the 96th percentile. Whether I have an explanation for something ("I forgot to take an insulin dose, and that's why this blood sugar is higher than I'd like") or not, I worry about it. I worry that my diabetes is hurting my baby.

According to everything I've read, the last trimester (particularly at 7 and 8 months of pregnancy) is the hardest for managing diabetes, because that's when insulin resistance is at its peak (thanks, placenta!). It may get a bit easier during the last few weeks, with insulin needs plateauing or even decreasing a bit as my body prepares for labor. And then, after labor and delivery of the placenta, my insulin requirements will likely go right back down to pre-pregnancy levels. Unfortunately, I don't know what those "pre-pregnancy levels" might be for me, since before my pregnancy I was 1) not taking any mealtime insulin, and 2) eating a low-carb diet to address that fact. I don't particularly want to go back to that (especially since I plan to breastfeed, and will likely need to maintain a fairly similar diet to what I've been eating while pregnant in order to successfully do so), but that means I don't know what my non-pregnancy insulin requirements will be, given that I've never regularly taken mealtime insulin when not pregnant. Maybe we'll start with the lowest doses I took during this pregnancy, and adjust from there?

I plan to write two future blog posts on these topics - one about managing my diabetes during the 3rd trimester and during labor, and another about managing my diabetes postpartum - but these likely won't get posted for quite some time. When my 3rd trimester is done, I'll have a few other things on my mind (a baby, for instance, and transitioning to motherhood!), but I'm hoping to have that 3rd trimester post available by March 2020, whether my little one arrives in January 2020 as my estimated due date would suggest, or in late December 2019, as my MFM doctors are likely to push for.


Friday, April 19, 2019

April 19

Today, April 19 is the due date my pregnancy would've had, if it had gone to term. When I miscarried back in September, this due date still felt very far away; I thought for sure I'd be pregnant again by the time April 19 finally rolled around, and be able to use that new pregnancy for solace. But trying to conceive after miscarriage has unfortunately turned into a longer journey than I anticipated, and as much as I wish I had good news to share right now - I don't.

There are days (this week in particular) when it's hard not to focus on the could've-beens, thinking about that alternate universe where my pregnancy went to term and I became a mother this week. There are other days when it's hard to remain optimistic about getting pregnant again. There are days when I feel like a failure. Though deep down I know it's not my fault and there's nothing else I could be doing right now to try to make this work, a part of me still feels like I'm letting everyone down (myself included) every month that my period shows up again. I feel like I'm depriving the people I care about from the happy ending they're waiting to hear.

In moments of defeatism, I have several quotes I turn to for inspiration. My favorite right now is this one, from Helen Keller: Remember, no effort that we make to attain something beautiful is ever lost.” I remind myself that even though we can't control the outcome, we can keep trying anyway... and then try to find hope in our resilience. Many days, this doesn't feel like enough. I want to do more than that, have control over more than that. But at least that's something.

These are not things we usually talk about. Worse, these are things that are hard to talk about. It's hard to post about disappointments and things that feel like personal failures - especially on social media platforms where most people only post their success stories, happy memories, and best selfies. It's hard to admit that there are things we can't earn just by wanting, just by trying. It's even hard to admit to wanting something at all, in a world that encourages us to blow out birthday candles and wish on shooting stars in silence. Not only is vulnerability hard - but, we are taught, also punishable. Share your deepest hopes and dreams aloud, and risk seeing them "jinxed" and never fulfilled.

But as hard as it is to be vulnerable - especially with something like this, where I'm still in the middle of the story, without any idea of how long I'll be here - it's also hard to be lonely. And going through a miscarriage and trying to conceive are often very lonely endeavors. When you're struggling with something privately, and your pain goes unrecognized, it's hard not to start feeling invisible. And that's a shitty thing to feel, on top of everything else.

Which is why I'm sharing all this. I debated with myself for a long time about whether or not to post anything, writing and rewriting several drafts over the last several days, weeks, months... Ultimately I decided that, at least this week, I want to be visible again (and I deserve to be). I want my experience to be acknowledged, my pain to be just a little less private - if only for a moment.

You can read more about my miscarriage here - the post I wrote last October 15 for Pregnancy Loss Remembrance Day.

Monday, October 22, 2018

Diabetes & Miscarriage

I have LADA (Latent Autoimmune Diabetes in Adults), which is essentially Type 1 but with an extended “honeymoon” phase at onset. My doctors first noted that I had slightly elevated fasting blood sugar when I got routine blood work drawn for an annual physical in 2012, when I was 23. Though I would never had any of the telltale diabetes symptoms (excessive thirst and urination) over the next five years, my blood sugar only continued to rise further into the “prediabetes” range, and my endocrinologist started me on a low dose of basal insulin in February 2017, when I was 28, to supplement the limited insulin my pancreas was supplying. (You can read more about my LADA journey here and here.)

I went into my first pregnancy this year both worried about how my diabetes might negatively impact my pregnancy and how my pregnancy might impact my diabetes. I was warned that getting pregnant might push me out of the “honeymoon” phase or otherwise complicate my LADA into looking more and more like a Type 1 with no remaining pancreatic insulin production - then again, I was also told that this would happen regardless, either on its current gradual path or all of a sudden, triggered by an infection (including something as common as a cold, the flu, etc.) or triggered by nothing at all but the passage of time. I knew my blood sugars were in a good range for trying to conceive and for being pregnant - but I didn’t know how long that would last. My body was already requiring more supplemental insulin as the months and years went by, regardless of whether I was pregnant or not; I figured getting pregnant sooner (while my pancreas still produced some of its own insulin) rather than later (when it might no longer do so) would only make it easier to keep my diabetes well-controlled during pregnancy. And if I did end up seeing my diabetes forever altered by a pregnancy? Well, I supposed that having a baby and becoming a mother be worth the sacrifice.

Not all pregnancies have a happy ending though. In September, my nearly 9 week pregnancy ended with a missed miscarriage and a D&C, leaving me to navigate the physical process and emotional grief of pregnancy loss (which you can read all about in my previous post). And unfortunately - though that would have been more than enough - that’s not all of the story. In a matter of weeks, I was hit with a double whammy of body betrayal - first, a uterus that could not sustain a much-wanted pregnancy, and second, a pancreas that succumbed (temporarily if not permanently) to what it had been hinting at for years: a further decrease in (or at least less predictable/consistent) insulin production.


I finally purchased a medical alert bracelet when I was pregnant, envisioning a time in the not-too-distant future when my pregnancy's second and third trimester would require me to take more and more insulin. A few weeks later, my pregnancy was over and I purchased another bracelet - this one featuring half-pink/half-blue Pregnancy Loss Awareness ribbons.

In the days/weeks after my D&C I saw enough “wonky” blood sugars to worry me and prompt me to look into ways of altering my diabetes treatment plan. I made appointments with my endocrinologist and maternal fetal medicine (MFM) at Beaumont hospital. I talked to sales representatives for two different brands of insulin pumps, and looked into continuous glucose monitoring (CGM) systems. And I searched for advice or stories online about people with diabetes who saw their diabetes treatment routines impacted by miscarriage - and couldn’t really find any. I was disappointed not to find more information - or at least personal anecdotes - and so I decided I could at least write down my own, to be found by other people who might also be searching.

To be clear: this is a post about how my miscarriage affected my diabetes - NOT the other way around. My diabetes did not cause my miscarriage. My A1C while pregnant was 5.4%. Anything below 5.7% is considered “normal,” the 5.7-6.4% range denotes prediabetes, and most people with diabetes are instructed to shoot for staying under 7% as a reasonable goal. For pregnancy, the recommended A1C target is <6% - if it can be achieved without hypoglycemia - a.k.a. low blood sugar. The higher someone’s A1C (a way to measure average blood sugar over a 3-month period), the likelier the chances of birth defects, preeclampsia, neonatal hypoglycemia, and yes, miscarriage - but with an A1C of 5.4% (comparable to many pregnant individuals without diabetes), my diabetes posed no great risk to my pregnancy and could not have caused my miscarriage. My obstetricians told me that my miscarriage was likely caused by the same thing that causes at least 1 in 4 known pregnancies to end in miscarriage: unpredictable, uncontrollable chromosomal abnormalities. When I met with my MFM doctor, he repeated the same thing, launching into an unprompted 15-minute explanation of how chromosomes work and telling me over and over again: “This was not because of your diabetes.”

I lost track of the number of well-meaning but misinformed people who asked me - sometimes obliquely, sometimes point-blank - if my diabetes was the cause (or a cause) of my miscarriage. Maybe they were thinking of the film/play Steel Magnolias - for many, the only cultural resource they have for a diabetic pregnancy storyline, in which (spoiler alert!) a woman with diabetes-related kidney problems was discouraged from her doctor from getting pregnant, and then suffered the fatal consequences when she intentionally got pregnant anyway. The pregnancy put undue strain on her already-failing kidneys, to the point where she required a kidney transplant three years after her son’s birth. She died when her body rejected the transplant. The story is based on the true story of the playwright’s sister, and takes place in the mid-1980s - when portable blood glucose meters were not yet widely available, let alone the insulin pumps and CGMs (continuous glucose monitors) we have now. Diabetes was thus a lot harder to control and resulted in more complications at younger ages.

The current 2018 reality is that women with pre-existing Type 1 diabetes successfully have pregnancies all the time. None of my doctors - including my endocrinologist and my ob/gyns - ever expressed concern about my diabetes impacting my ability to get and stay pregnant. In fact, throughout my nearly 9 week pregnancy, I was the one who kept pushing for information, advice, and more appointments; I practically begged my providers to treat me like a high risk pregnancy and go over my blood sugar logs with me, and still they refused. I have only one and a half years experience taking insulin - and that experience encompassed only basal insulin (mainly to help with my fasting glucose numbers); to control post-meal blood sugar spikes I was instructed to limit my carbohydrate intake. So I had a lot of questions about what to expect while pregnant, and whether or not I should be continuing my lower-carb diet or beginning bolus (mealtime) insulin - and it was so aggravating when I struggled to find anyone in the medical profession who would answer my questions for me.

When I told my endocrinologist a year in advance that we would be trying to conceive soon, he told me that I would likely have to start bolus insulin once I was pregnant - but once I got my positive home pregnancy test and notified his office that I was pregnant, he wouldn’t give me any advice or update my insulin prescriptions. Instead, he told me that he “doesn’t see pregnant patients” and that I would need to contact MFM at the hospital to handle the ins and outs of my diabetes. Then, when I tried to set up an appointment with MFM, they couldn’t get me in until I was 9 weeks along. (I ended up having to cancel that appointment when I had my D&C at 8 weeks 6 days.) Whether it was because my insulin needs were still slight, or because having diabetes just isn’t considered much of a high risk anymore as long as it’s kept under good control, I don’t really know - but from my standpoint it was very frustrating to me that I was denied the care and reassurance I was looking for.

I work really hard to control my diabetes every day - but I especially did so while I was pregnant. As I said, I didn’t really have any guidance from any of my doctors about how to proceed (though my endocrinologist did recommend I start taking a bit more basal insulin in the morning, to supplement the basal insulin I was already taking at night). I also didn’t have a prescription or even any samples of a quick-acting bolus insulin, and no one - not my endocrinologist, not my OB, and not my MFM doctors (because they hadn’t seen me yet) - would write me one. I had to be so careful with what I ate - and how much - because all I had was basal insulin and my diet to try to keep my blood sugar levels within the impossibly tight pregnancy target ranges of <90 dL/mg when fasting and <120 dL/mg two hours after eating. When I talked to my OB at my 6-week ultrasound, I told him what some of my higher numbers were, and he condescendingly said: “Those aren’t good enough. Do you think you can do better?” It took everything in me not to start crying. I said: “I’m already doing all I can! I can’t do anything else to make these numbers better until I have mealtime insulin I can take!” He changed his tune after that. “Oh. Well you know, these numbers are actually pretty good if you don’t even have mealtime insulin to work with. You’re fine.” And still he wouldn’t give me any bolus insulin.

From the day I saw that positive home pregnancy test until the day of my 8-week ultrasound (when I learned the news that I was having a missed miscarriage), I counted calories and carbs every single day, and I started eating fewer and fewer carbs in an effort to try to hit in-target after-meal glucose numbers. There were some days when I ate only 75 total grams of carbs in 24 hours. I worried about not getting adequate nutrition by keeping such a low-carb diet, but I had no one to ask what was worse for my growing child - a lower-carb diet or higher post-meal glucose readings - because none of my doctors would advise me. (And before anyone asks - a lower-carb diet, while maybe not the best nutritional choice for pregnancy, does not cause miscarriages and also cannot be blamed for mine.)

A friend asked me, when they saw how much effort I was putting into making healthy food choices, if it was easier to stay motivated to keep my “diabetes diet” now that I was pregnant. The truth is that motivation has never really been an issue for me - I was already doing more than what my doctors had asked me to do to try to keep my glucose in check. Instead, it just made me all the more anxious and self-hating anytime I saw numbers I didn’t want to see, because now it wasn’t just going to potentially affect my health, but my baby’s as well. My pancreas doesn’t work properly, and like any person with diabetes, I am sometimes going to see too-high numbers, even when I’m doing everything I’m “supposed” to be doing. I can’t control everything. But I tried to control everything anyway, and the few times when I saw a post-meal spike approaching or even well into the 200s, I was devastated. I felt horrible and guilty and like I wasn’t doing enough - even though I was literally doing all I could do.

My endocrinologist tried to reassure me that a few high numbers here and there were not a problem, and that as long as my A1C stayed below 6, I was not as risk for any complications. When I miscarried, the OB who saw me that day repeated the same thing. “It wasn’t anything you ate or drank that caused this,” she told me. “And it wasn’t any funky sugar issue. These things just happen. There was nothing you could’ve done differently.”

If I sound a little defensive, it’s because I am. There is a difference between controlled diabetes and uncontrolled diabetes - and in 2018, diabetes can be more or less controlled, as long as someone is motivated and educated in what to do, and has access to the medication and support they need. All of the serious diabetes-related risks you hear about (kidney failure, blindness, amputations, and heart attacks/strokes) are risks for uncontrolled diabetes, and are typically associated with A1Cs in the 10-13% range; the woman with diabetes in Steel Magnolias, then, likely had an average A1C twice what mine was. People with diabetes who can consistently keep their A1Cs under 6 are essentially just as healthy as anyone else without diabetes - it just takes them more effort (sometimes a LOT more effort) and daily management to be that healthy, rather than seeing their bodies do it naturally. When people ask me if my diabetes caused my miscarriage then, it sounds accusatory to me. It sounds like they’re asking if I wasn’t controlling it enough, if I wasn’t putting in the effort and daily management. And I was. I was doing everything in power to prevent a miscarriage, and still it happened anyway.

But as I said - that’s not what this post is about. My diabetes didn’t contribute to my miscarriage - but my miscarriage did impact my diabetes, and that’s what I wanted this post to be: a testimonial of how my LADA changed in the weeks after my miscarriage, the likes of which I sought out for camaraderie and reassurance and was unable to find.

When I had my D&C on September 13, I was in the hospital for about 3.5 hours. The actual procedure took less than 20 minutes; I was under general anesthesia for about 40 minutes total. Because I couldn't eat the morning of the procedure, I went slightly low (67) while under the anesthesia. I was given apple juice when I woke up, and after drinking the juice and going home and eating lunch, my blood sugar then shot up to 325, the worst I've ever seen it - and not something I particularly wanted to see on a day when I was already anxious about the possibility of infection. Talking with my endocrinologist six days later, he said he wasn’t surprised - high sugars are apparently often part of a typical inflammatory response for a person with diabetes following an invasive procedure - but it was still frightening for me to see at the time. At that point, I still had no mealtime insulin to use to get that 325 glucose down; neither was I in a state where I could exercise or do anything else that might help, since I was supposed to be taking it easy and resting after the procedure. I checked my glucose every hour and watched impatiently, stressfully, to see it go slowly back down on its own (294, 233, 217…). I messaged my endocrinologist the next day, asking if I could please at least get some sample bolus insulin pens to use in the hopefully infrequent emergency situations where something like this might happen again. I also told him that I had miscarried, but that I wanted to try to get pregnant again. Now that I was no longer pregnant, he agreed to meet with me, and the aforementioned six days later I went in for an appointment.

First, he finally gave me the bolus insulin samples I’d been requesting for months - two pens of Humalog. Second, I noticed that on the paperwork they use to code the visit for insurance purposes, he circled “Type 1 - Controlled” for the first time; at all previous visits over the last three and a half years, including the one where he started me on basal insulin one and a half years ago, he’d circled only “Elevated Fasting Glucose.” (There is no option for “Type LADA.”) Third, he asked me if I had any interest in getting a CGM (continuous glucose monitor) and/or insulin pump, which I might find useful for a subsequent pregnancy. I don’t know if it was my glucose finally topping 300 once, or if it was my “threat” about trying to conceive again - which he was apt to take more seriously this time, now that I had already done so once; whatever the reason, I finally saw myself treated less for the “latent” part and more for the “autoimmune diabetes” part of the LADA description. I resented that I had to go through a pregnancy and miscarriage to get the attention and resources I’d been requesting all along, but I guess now I can count it as a thin silver lining in the middle of a tragedy.

My endocrinologist warned me that if I waited until 2 hours after eating (which is when I usually check my glucose), it would then be “too late” to take Humalog. It peaks 1-2 hours after eating, to counteract the food that was consumed, and so if I took it 2 hours after eating it wouldn’t peak until 4 hours after eating, and then I would risk hypoglycemia. He said if I already had high glucose (>150) before eating, then I could take 2-3 units of Humalog with my meal. I was a little disappointed in these instructions - first, because it meant I’d have to start sticking my finger even more frequently to check my glucose levels, if I had to now test before eating as well as after eating; second, because I’d seen several instances where my glucose was on or near target before eating, but then still got high after eating, and if I followed his rules I still wouldn’t be able to treat those highs. But at least it was better than nothing, and I figured it would at least be useful on a day like my D&C, where even if I couldn’t have prevented that first 325 high, I could’ve at least eaten dinner when I was hungry (instead of waiting 6 hours after lunch to eat dinner, to give that 325 time to finally get below 150 again).

It turned out, though, that I would get to use the Humalog sooner than I anticipated. I work part-time and get home around 1:45 pm, typically eating lunch around 2 pm. If I also happen to eat an early-ish dinner that day - at 5 pm or so - that makes it only three hours between meals. If I get a higher number after lunch, then, it might still be at or above 150 when it’s time to eat dinner. Lunch didn’t used to be a problem for my blood sugar - my numbers after breakfast and lunch tended to be pretty good, while I still had more basal insulin in my system; if I had a problem, it would likely be with dinner. But a few days after my endocrinologist appointment, I started seeing higher numbers after lunch - for no real reason that I could figure out. September 26 - thirteen days after my D&C - I took my first mealtime insulin. Because I was also still continuing my twice-a-day basal regimen from pregnancy, that made three times that day when I was injecting insulin - and ten times that day when I checked my blood sugar with a finger prick. I’d been researching CGMs and insulin pumps since my endocrinologist brought them up at the appointment; if my body was going to make this a regular thing of requiring mealtime insulin after all, the idea of getting both was looking better and better.

In the weeks after my D&C, I also saw several episodes of mild hypoglycemia (blood sugar less than 70), all in the middle of the night or early morning: 65 at 1:30 am on September 16, 61 at 3:25 am on September 24, 68 at 6:10 am on October 1, 59 at 1:25 am on October 3… These are just the ones I know about - the ones that woke me up feeling warm, sweaty and shaky, or feeling hungry and otherwise “off.” There was also the night of September 27 when I had several dreams about feeling hypoglycemic, and I kept waking up or almost waking up throughout the night. I don’t know if I actually went low, or if I was just worried about it (it was the night after I took Humalog for the first time, so I’d taken slightly more insulin than usual during the day), because I wasn’t conscious and aware enough to figure out if I was having hypoglycemia symptoms while awake, rather than just in a dream, and I never tested. My fasting glucose that morning was 88 - right on target - so I suspect they were just anxious dreams. But many people with diabetes experience what is called a “predawn” phenomenon, where their blood sugar rises (sometimes significantly) when they wake up, and it’s certainly possible that I was in the 60s overnight and then still got a healthy 88 when I tested before breakfast at 7 am. As far as I know, I have no hypoglycemia awareness and the symptoms always wake me up - but as I haven’t used a CGM to track my glucose overnight, and am not in the habit of setting an alarm for 2 am to wake up and check regardless of how I feel, I don’t actually know if that’s true. I might be going low even more often than I realize.

I’m not sure if my hypoglycemia was caused by a slight decrease in insulin needs once my body readjusted to a state of non-pregnancy after my miscarriage - or if I kept going low because I wasn’t eating enough. Three of the four nights listed above happened after days when my schedule deviated a bit from my norm and I ended up eating less than 1700 calories and/or less than 100 g. carbs throughout the day - but the other one was after a day when I ate nearly 2000 calories and 134 g. carbs, and there were also several other days during those first three weeks after my D&C where I ate less than 1700 calories and/or less than 100 g. carbs and didn’t go low at all (that I know of). My impulse is to always look for the pattern - but sometimes it seems like there isn’t one, which is frustrating. To make matters more confusing, there were other days - about once or twice a week - when my fasting glucose was slightly high (above 100) in the morning, making me wary to just decrease my basal insulin every day as a solution for treating hypoglycemia - because then, I worried, my fasting numbers would just grow worse.

The answer, I think, is to somehow fine-tune my insulin intake at meals throughout the day so that I’m not relying so heavily on basal insulin (and probably to change my eating habits to be more steady and predictable from day to day, as well) - but I for awhile I debated if it would be better to do that by employing more Humalog insulin injections, or by switching over to an insulin pump. With a pump, I would be able to control my basal insulin as a gradual release with a little bit every hour, which better mimics the insulin production of a properly functioning pancreas - rather than taking two blanket doses (one in the morning, one in the evening) in an attempt to cover the entire 24 hour period, like I do right now. It’s a question that depended on a lot of factors, including what my insurance will actually cover (given how low my A1C already is with my current regimen), how much my blood sugars might fluctuate in the weeks/months while I adjust to a new insulin delivery schedule, and how soon I plan to try to get pregnant again.

And in case that wasn’t enough information overload for you - there’s more! At the beginning of October, I finally got my long-awaited appointment with MFM. It was considered a “preconception consultation” now that I was no longer pregnant, and I was worried that after so many weeks of hoping and waiting to talk to them, through pregnancy and miscarriage and recovery, it would be a quick, disappointing consultation that still left me with unanswered questions. Thankfully, everyone in the MFM department was great - once I finally got in there - and the doctor talked to me for nearly an hour! (How often do they actually give you that much of their time and undivided attention??) The doctor I spoke to was adamant that with an A1C of 5.4% I was clearly doing all the right things already; still, when I brought up that I was only keeping my A1C so low because I was doing a low-carb diet, he listened to my concerns instead of dismissing them. He said that I should feel comfortable eating a healthy, balanced diet that would include 150-200 g. of carbs per day (whether pregnant or not), and that if I can’t do that without taking mealtime insulin, I needed to be taking more mealtime insulin. It was exactly what I wanted to hear - that I didn’t have to play this awful game of prolonged extreme dietary self-control anymore, denying myself even appropriately-sized portions of healthy carbs in an effort to control what my pancreas could not. (During the month of September, I ate only 60-130 g. of total carbs every day - most of which were healthy, low-glycemic carbs from vegetables, beans, and fiber bars.)

I further told him that my endocrinologist had only just given me Humalog to use “on a case by case basis,” that so far I had only used it once, and that my endocrinologist had not told me what carb-counting ratio to use, encouraging me to use “no more than 2-3 units” with a meal (regardless of how many carbs that meal included), and only then when my glucose was already slightly high before eating. Maybe that’s fine advice for someone like me in general, whose insulin needs are still relatively small and only gradually increasing. But I knew (and the MFM doctor agreed) that I would likely need to be able to employ carb-counting ratios to figure out tailored bolus doses when I got pregnant again, and that it would be better to learn how to appropriately use bolus insulin now - before I got pregnant, started developing more insulin resistance around the second trimester, and REALLY needed it. He assured me that they would be able to help me manage my diabetes while I was pregnant - no separate endocrinologist needed - and he referred me to their dietician/nutritionist for tips on how to incorporate more healthy carbs into my meal plan to get up to 150-200 g. a day.

To be clear, I don't (fully) blame my endocrinologist for my low-carb diet. For one thing, even though I listed my daily carb counts on every blood sugar log I gave him, I don't know if he ever paid any attention to that column. I don't know if he realized how much I'd pared my carb intake down to maintain on-target glucose, since it happened gradually over time and especially during my pregnancy - when he wasn't paying attention, because he “doesn’t do pregnancies.” For another thing, though - I started seeing him back in 2015, when my c-peptide levels (the amount of insulin my pancreas still produces) were still in the normal-ish range, and for a couple years I was easily able to keep a relatively good A1C just by watching what I ate. When he started me on basal insulin in early 2017, my c-peptide levels had gotten worse - but I was still clearly producing much of my own insulin, and needed only to supplement it with a little bit. When it's such a gradually declining slope like that (like it is with all LADA, but, he has said, with me especially, who's been experiencing what he has in the past called "one of the longest honeymoon periods he's ever seen"), it's hard to know when you've crossed over the line between being able to maintain steady blood sugar with diet changes alone and needing to admit that diet changes cannot cover it anymore. Furthermore, I was also (and still am) rather sensitive to insulin, which is why I get hypoglycemic so often. I don’t need much insulin at all, and there is a real risk to prescribing me too much. So it does make sense that he would hold back and want to avoid putting me on mealtime insulin for as long as possible - but it’s also been clear to me, for at least the last several weeks, if not months, that the time has come to stop avoiding it and instead embrace bolus doses as part of my everyday. And it was nice to have the MFM doctor agree with me.

I next asked my MFM doctor if I should get an insulin pump instead of doing manual mealtime injections. (I just wanted someone to tell me what to do, so I didn't have to make the decision myself.) He didn't help. He said that it was up to me - but if I wanted to switch to the pump, I should definitely do it now... and then wait at least three months before trying to get pregnant again, to make sure my blood sugars are stabilized with my new regime and my A1C is back on target for pregnancy. I didn’t know if I wanted to wait that long before trying to conceive again - especially once I factored in that it can sometimes take awhile to jump through all the necessary insurance hoops and receive a pump in the first place, which would push a potential second pregnancy even farther into the future - but I also didn't want to deny myself the opportunity to have more resources at my disposal just because I still wished my first pregnancy had never ended early, and I was impatient to be pregnant and feel hopeful again.

The doctor also said that a pump was definitely not necessary for me, given that my A1C was already so good without it and that the medical profession often takes on an attitude of “if it ain’t broke, don’t fix it,” not wanting to disrupt a good thing. Of course, I suspect that just increasing my carb intake and my bolus insulin, and likely adjusting my basal insulin down to compensate for the bolus doses, will already “disrupt” the good A1C I currently have, at least for a couple weeks while I trudge up the learning curve of figuring out how to correctly count carbs and utilize an appropriate bolus carb-insulin ratio. My gut reaction, then, was to suggest that if I’m going to see temporary problems while I fine-tune my insulin anyway, maybe switching to a pump wouldn’t be that much of a difference during the transition period, while ultimately (probably) giving me better insulin control in the end. On the other hand, I also worried that maybe skipping right to a pump and trying to do everything all at once would be overkill. It would be good to know how to figure out my bolus ratio myself first instead of jumping immediately to a pump and relying on its calculator to determine my ratio every meal - because if I don't know how to do it myself and then something were to happen to my pump, I'd be inexperienced and lost trying to figure out how to do it by myself on the fly.

At the very least, I would love to have a CGM. Then, instead of only having data of my blood sugar levels during the times of day when I can prick my finger, bleed on a test strip, and check my glucometer, I could easily just consult the CGM screen/app to see automatic readings of my glucose every five minutes. It would also alert me if I was trending toward hypoglycemia, so I could correct it faster before I went too low (and maybe catch some more instances of it if it turns out I am going lower more frequently than I realize). I would love to have access to all that data. But I couldn’t even get a CGM until I first made a decision about the pump - because getting a pump would change which brand of CGM I got.

For my needs, it seemed like the Dexcom or Medtronic CGMs would work best. The downside of the Medtronic CGM is that it requires an Apple device to see the data, and I only have an Android phone. I was told by the Medtronic representative that they expect to have their app available on Android phones “any day now” - but that “any day” could be as late as mid-2019. To use their CGM, then, I would need to switch to an Apple phone or purchase an iPod touch. The Dexcom, on the other hand, comes with its own Dexcom-specific monitor so I wouldn’t have to purchase another device - and therefore seems like the easier choice if all I’m getting is a CGM. If I did decide to get a pump, however, the Medtronic makes more sense - because the Medtronic insulin pump (which seems to be far and away the most accurate on the market) works as a hybrid closed-loop system with their CGM, meaning that the pump can automatically adjust doses or temporarily suspend insulin based on readings from the CGM.

There’s also the maintenance and aesthetic of these wearable technologies to consider… The Medtronic hybrid system has the CGM sensor (which you have to change every few days) and its rechargeable transmitter, plus the insulin injection site (which you also have to change every few days), cumbersome tubing, and the bulky pump itself, which has to either hook onto an article of clothing or fit inside a pocket - and was thus obviously invented by men who don’t understand how tight or thin the fabric often is or how small the pockets often are on women’s clothing. It sounds great in theory to have what is essentially an “artificial pancreas” (or as close as we have to that right now) - but the actual day-to-day of wearing all of those pieces seems very daunting to me, especially when it’s not necessary for me to do to maintain tight blood sugar control and my MFM doctor thinks I’ll be just fine for the entirety of my next pregnancy without it if I'd rather stick to multiple insulin injections.


It’s just all a lot to think about - and I felt like I had to make a decision relatively quickly, before I could move forward toward my goals of pregnancy and motherhood again. Because I kept going back and forth on it, my husband advised me to just get the CGM for now, and then revisit the idea of a pump in a year or so. I already have more resources at my disposal than I had last time - I’ve talked to MFM, I know who will be helping me with my diabetes during pregnancy, and I’m starting on a diet and insulin adjustment plan; it’s likely these would be enough to give me peace of mind (as much as anything could) whenever I get pregnant again next. So I contacted Dexcom and am expecting to hear back soon from them about what my insurance will cover. It's so important to me to have a CGM that I'll probably pay for whatever the out-of-pocket cost happens to be... but I obviously hope it won't be too astronomical. Once I have my CGM, I'll feel more comfortable experimenting with bolus insulin to fine-tune what my mealtime ratio should be, and hopefully I can work out something there that will work for me without too much hassle.

I know this is a lot of tedious information, especially if you aren't familiar with the ins and outs of diabetes management. I just wanted to outline all the things that have been weighing on my mind lately and the decision process I recently went through to illustrate why it's so easy to get overwhelmed and feel angry. Why can’t my pancreas just function properly so I don’t have to deal with all these issues, put in all this effort, go to all these appointments, and make these difficult decisions? Why couldn’t my first pregnancy have just worked out, so that all these decisions about my diabetes management would have been postponed for another time? I didn’t do anything to deserve any of this, and it isn’t fair.

It’s been a stressful couple of months. Sometimes I feel like I’m not allowed to admit that and show people how sad and frustrated and overwhelmed I am. I have to remind myself that that isn’t true, that my feelings are normal and valid, and that anyone would feel sad and frustrated - because these are sad, frustrating things. I’ve been (mostly) feeling a lot better emotionally about my pregnancy loss over the last few weeks (something that’s possible only when it’s no longer actively happening) but my diabetes management is still an occasional great source of stress for me, and likely will be on and off for the rest of my life. Diabetes isn’t something that just goes away. It’s always there, impacting all areas of my life and requiring a lot of my time and energy to manage - particularly in times that are already stressful, such as during and after a miscarriage, or during pregnancy. Stress makes diabetes management less efficient and predictable and diabetes itself can further contribute to stress - and I feel like people don’t talk about that enough.

Saturday, January 21, 2017

"28 Years" - Explanation of Years 15-28

As part of my "research" for planning my new colored pencil drawing, "28 Years," I went through old journals, drudged up memories, and decided what two flowers would best symbolize each of the years of my life.

Yesterday's post talked about the symbolism for Years 1-14. Today, I'm going to focus on the last two rows, row 3 & 4, which will represent Years 15-28.

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Year 15 (2003)
  • Cherry Blossom: symbol of transience, good education, womanhood, love, wisdom, and the short lived beauty of youth
  • Fern: symbol of sincerity
This year was the year that I was 14. My dad finally found new work after fifteen months of unemployment. I finally got my first period, years after I thought I might. And I started my sophomore year of high school. In my journal I wrote, "I'm not supposed to feel. I'm not supposed to care. I should be above this stuff, this human emotion. I'm better than this." Another day, I wrote, "For now I guess I'm stuck being me. Maybe one day that'll make me happy. Maybe one day I'll be proud of myself." None of my friends had the same lunch as me, so I did my precalculus homework during lunch and wallowed in self-pity. I often felt very lonely, and like I wasn't good enough, but I put on a brave face, same as always. I joined Drama Club and tried to make new friends.

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Year 16 (2004)
  • Marigold: symbol of pain, grief, cruelty, jealousy, beauty, warmth of the rising sun, creativity, and a drive to succeed
  • Hollyhock: symbol of ambition, abundance, and fertility
This is the year I was 15. I had some of my worst classes this year - not academically, but emotionally. I had a lot of classes where none of my friends were with me, and I felt very alone. As part of our physical fitness requirements, we had to do a swimming unit, and I struggled with feeling comfortable with tampons. I wrote in my journal, "I'm not perfect. I'll never be perfect. But try telling my brain that. I've been told all my years that I'm capable; I can be anything I want to be. So I have to be everything I can be. Anything less is disappointment." I also wrote, "Am I ugly? Am I too shy? How can I become more outgoing? Why does no one like me?"

I started junior year and took three AP classes. I was constantly comparing myself and my grades to my friends. Any bad feelings or stress I had I was just burying deep inside so no one would know how sad I was.  I wrote, "I'm drowning / My throat's closing on me / There's no more air / A savior is what I need / To get me out of there." I started questioning the religion I was brought up in (but silently, only silently, in my head). I wrote tragic stories where horrible traumas happened to my characters. I wrote, "Imagination is so much more than real life."

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Year 17 (2005)
  • Tansy: symbol of hostile thoughts, health, and longevity
  • Purple Hyacinth: symbol of sorrow, regret, grief, and pleas of forgiveness
This is the year I was 16. One of my closest friends was upset with herself (in much the same way I was upset with myself), and I had such nice things to say to her, to try to cheer her up. To myself, I was much meaner. In my journal, I wrote, "I know I'm in a self-deprecating mood, but I don't give a shit. I'm sick of crying these god damn self-pity tears but I can't get out of this funk." I also wrote: "Please. Just make the world fuck off. I'm sick of all this shit. I just want to scream and cry and hope that one day I stop being a bitch. I'm so horrible. I don't deserve to live." I spent the summer in France, spending three weeks with a French family. I started senior year. Some of my friends started dating, and I felt left behind. 

I wrote: "She's put herself on a pedestal / All she can do is fall / Can't meet her own standards / No one else comes to her rescue / They are too busy also holding themselves up to high standards." I also wrote: "How can any God, any Creator of the universe, love someone who hates herself so much?"

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Year 18 (2006)
  • Zinnia: symbol of endurance, lasting affection, daily remembrance, and thoughts of absent friends
  • Dandelion: symbol of resilience, overcoming hardship, healing from emotional/physical pain, emotional/spiritual intelligence, survival, long-lasting happiness and youthful joy, and getting wishes fulfilled
This is the year I was 17. My New Year's Resolution was: "Be super happy with myself and love myself. Fill any void in my life that way instead of looking for someone else to do it for me." I "forced" myself into the drama club - when I didn't get a part in the play, I got involved in behind-the-scenes crew, so that I would have fun things to do, ways to destress, and opportunities to make new friends. In my journal, I wrote, "I fear success. I fear the new situations and new feelings that might come from dating someone. I fear loving someone too much. I fear rejection, too." I was not happy with my grades, my SAT scores, or my college acceptance letters. Good news meant nothing, and bad news meant everything. Still, I tried to be brave, and confident. I wrote, "I need to live in my imagination less and focus on the real world. I need to be more confident in myself and my abilities." I wrote, "I'm nervous. I just want to stay in high school forever. I know high school. I can do it well. College is going to be different. And I'll revert back into my shell like a scared turtle and never say a word and be so quiet that no one will befriend me." 

I took AP art and grew as an artist; I decided to major in art in college. I graduated high school and started at EMU. I wrote, "I hate feeling depressed and self-loathing and yet I do it all the time. I hate myself for hating myself." Friendships from high school changed and faded once we no longer saw each other every day. I felt like I didn't belong in college; I felt like a fraud. I wrote, "All day it has kind of felt like a dream. Everything seems off. Nothing matters because today is all a dream and I'm going to wake up soon. Nothing can hurt me today; I am invincible."

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Year 19 (2007)
  • Protea: symbol of change, resourcefulness, daring, transformation, diversity, courage, hiding thoughts/knowledge and keeping things to yourself
  • Hydrangea: symbol of heartfelt and honest emotions, gratitude at being understood, opportunities for love, a deep understanding between two people, frigidity, and apology
This is the year I was 18. I wrote, "Sometimes I need to hear that I'm beautiful or intelligent or loved. And I think that's a reasonable request. That's not being selfish. Everyone in the world deserves to hear those things." Another day I wrote, "If Christianity is right, and there is a hell, I am going to it. I'm ungrateful and selfish and demanding and awful. If I wasn't already on the list, I am now. I'm writing down my own name. I'll condemn myself. It's where I belong." Still another day, I wrote, "I am above this blindly believing in God shit."

I met the man who would one day become my husband - we talked online, we hung out as a group with friends, and we started dating. I got a job in the art department. I showed a collection of self-portraits at the EMU symposium and felt pretty damn proud of myself. I wrote, "If I'm confident in my abilities, I'll be amazed, I think, of what I can accomplish. I have always been (to some extent) confident in my intelligence and my artistic abilities and I think that has a lot to do with my success in those areas. But I could do with more confidence - in my looks, in my personality, in my value as a friend and as a person." I wrote, "I am proud of the person I'm becoming. I may be lonely and I may be insecure and I may have bitchy moments but I'm also becoming more comfortable with myself." Summer was lonely again (my boyfriend went home to Maryland), and the start of college's sophomore year was rocky - my mom was in the hospital, and I had new roommates and struggled to open up to them, or to try to make new friends - but I also worked as a teaching assistant for an art history professor, and I loved my classes and the amount of control I had over picking which ones to take.

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Year 20 (2008)
  • Red Tulip: symbol of true love and declarations of true love
  • White Jasmine: symbol of sweet love, beauty, sensuality, purity, good luck, love, and respect
This is the year I was 19. My boyfriend gave me a promise ring. I switched from a drawing concentration to watercolor and graphic design. I studied abroad in Switzerland, Italy, and Greece for five weeks over the summer. I started junior year and had new roommates again. I fell into old patterns of shutting myself down and not allowing myself to make new friends, but I also grew closer to my boyfriend. I knew I could always be honest with him. I worked as a tutor for art history. I continued to love my classes.

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Year 21 (2009)
  • Acanthus: symbol of art, enduring life, pain, sin, punishment, and mourning
  • Amaryllis: symbol of pride, worth beyond beauty, splendor, strength, and self-confidence
This is the year I was 20. I was getting toward the end of college and worried about my future. In my journal, I wrote, "It sounds dramatic to say that he helped me out of a dark place, but that's exactly what he did. I was lonely and depressed, at a school without any friends. I felt like I had driven all those closest to me away. He made me feel loved again. He made me feel like I mattered." I also wrote, "It's time to open up. That's my problem - not opening up about shit. It's time for my art to mean something."

I got a new job - working as a graphic designer for EMU's Campus Life. I got a new dorm, one without any roommates this time, so I could feel comfortable just being myself. And in October, Mike and I got engaged.

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Year 22 (2010)
  • Purple Iris: symbol of wisdom, compliments, eloquence, good news, royalty, faith, hope, and a bridge between earth and heaven
  • Love Lies Bleeding (Amaranthus): symbol of hopelessness, hopeless love, compassion, and sacrifice (especially the self-sacrifice of Jesus)
This is the year I was 21. I finished my thesis watercolors and my thesis paper and graduated EMU. I felt like I was getting recognition I didn't deserve - or maybe, for the first time, I actually felt like I deserved it. I moved into an apartment with Mike, went on a Mediterranean Cruise with Mike's family, and started planning our wedding. I tried to find a graphic design job in the Grand Blanc area but couldn't. I was kind of listless, not sure where to go now that I had completed the one solid goal I had always had (go to college). I wrote, "I just have no motivation. I kind of feel depressed. I don't know if I'm just not ready to give up on childhood, not wanting to get a real job; or if I don't feel like I'm good enough, worthy enough to get hired; or if I just don't want a job like the ones I've been looking into. I don't like not having a concrete next step." I wrote, "Some days suck. Some days I hate myself for being such a worthless failure of a person. I just don't do anything. I'm not good for anything. I'm not productive, I'm not contributing anything to society, I'm no good to anybody. I could write a longer list of self-insults, but I've done all that before."

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Year 23 (2011)
  • Peony: symbol of a good marriage, a good life, compassion, honor, wealth and riches, romantic love, beauty, bashfulness, and shame (especially of nakedness)
  • Myrtle: symbol of marriage, true love, good luck in love and marriage, chastity, marital fidelity, and prosperity.
This is the year I was 22. In my journal, I wrote, "I ignore big problems until they go away. I focus on little details. I make small, stupid things big and important because that's easier to do." I wrote, "There are certain things about myself that I've always been sort of frustrated with, downright disappointed in, and felt like I needed to change. Like being more outgoing and more confident...I've decided to stop thinking of such things as wrong, or bad, or shortcomings. These things are a part of me - they're a part of who I am, at least at this moment, if not for all time - and I need to learn not just to accept them as a part of me, but to grow to love them and cherish them as things that make me or my situation unique or interesting - things that make me me." Mike and I married in July. We honeymooned in Greece (Santorini and Mykonos). I still did not have a (paying) job. I tried to start a business, Invites by Andrea, and designed sample stationery to showcase what I was capable of.

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Year 24 (2012)
  • Pansy: symbol of thoughts (especially lover's thoughts), remembrance, and consideration
  • Daffodil (Jonquil): symbol of rebirth, new beginnings, uncertainty, returned affection, springtime, creativity, inspiration, renewal, vitality, awareness, inner reflection, memory, and forgiveness
This was the year I was 23. My husband and I bought a house and moved to Rochester Hills. I started working retail at Charming Charlie, while continuing to work in my spare time on the occasional invitation freelance job, my "Ideas by Andrea" blog, and my art projects and novel writing. It might seem strange that I felt better about myself, "just" working retail. But I felt like I was making positive steps in the right direction, that I was at least contributing something to society again, and that there were people who relied on me. 

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Year 25 (2013)
  • Purple Carnation: symbol of capriciousness, whimsy, changeable natures, and unreliability
  • Four o'clock Flower (Marvel of Peru): symbol of timidity, afternoon, and nighttime beauty
This was the year I was 24. I worked at Charming Charlie most of the year, but felt that working there more than a year would not continue to be steps in the right direction for me. I didn't want to stay too long that I felt stuck there, or that I stayed there because of a sense of obligation or fear of leaving and trying something else. I applied for substitute teaching certificates. I was pretty sure I didn't want to be a teacher - but then again, I had considered it as a possible career long ago, so what if I was wrong? In my journal, I wrote, "Keep on trying; you'll never win / Lock and key; you can't get in."

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Year 26 (2014)
  • Lettuce: symbol of never giving up
  • Lavender: symbol of purity, silence, caution, serenity, calmness, devotion, virtue, wishes coming true, grown-up femininity, refinement, grace, elegance, delicateness, and preciousness
This was the year I was 25. I quickly realized I hated substitute teaching, but I continued to do it because I felt that we needed the money, that I needed to contribute something, and that somehow, it might be good for me if I kept at it. I also, of course, continued to work (as always) on my art and creative writing in my downtime. I chose which days to work as a sub, and ended up choosing fewer and fewer days - because I'd rather spend my time once more stuck in my imagination than in the real world.

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Year 27 (2015)
  • Sage: symbol of wisdom, immortality, and a long life
  • Goldenrod: symbol of encouragement, money, and precaution
This was the year I was 26. I had some gastrointestinal issues which were probably linked to stress rather than any particular physical cause, and it was finally this that prompted me to see a therapist. All the low self-esteem and warning signs I'd written in my journal for years, always that nagging thought in the back of my mind that therapy might help, and it took physical symptoms to admit to myself that I couldn't continue on indefinitely the way I had been trying. Dysthmia (continual low-grade depression) and avoidance personality disorder were discussed, researched, considered. I quit subbing. We adopted Ginny. I worked on my story a lot, and sent out my first query letters (which were rejected).

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Year 28 (2016)
  • Bells of Ireland: symbol of luck
  • Gladiolus: symbol of strength of character, remembrance, honor, faithfulness, and conviction
This was the year I was 27 (last year). If you follow this blog, you know what I was up to this year, because I've already written about it. I had artwork shown at local galleries, got back into acrylic paint, did a lot of colored pencil work. I started a part-time graphic design job at Temple Israel. I edited my novel(s) and sent out more query letters (all of which were also rejected). 

I am not the same person I was at 15, or 20, or 25. And yet, I still am.

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I don't know what Year 29 will bring, or what flowers will best symbolize it when I reflect on its twelve months in hindsight. But these are the symbols I've decided for the years of my life which have already occurred, and the flowers I will be drawing in my new piece, "28 Years."

Obviously, not all of the things listed for each flower are ones that apply to me - especially since many of the symbols actually contradict each other. But I included all of the differing symbols anyway, just to show the possibilities which it might represent.

I am excited to continue work on this drawing. Now that all the research and planning and reflecting is set up, the drawings themselves should go pretty quickly. :)