letters to little liberte: 03

hi adeline,


This is the very first picture of you. Daddy took it. I hadn’t even seen you yet — the NICU team had to take you right away to make sure you were given the immediate care you needed.

You were born on April 26, 2023 at 6:46 p.m. You weighed just 4lbs 5.6oz. You weren’t supposed to come for 10 more weeks.

Dubbed our sunshine girl, you were born on the first 70-degree day we had since last October.

I wasn’t sure when I’d be ready to write your birth story — and to be honest, I’m not sure I’m ready now —, but I still remember it like it was yesterday and I don’t want to wait too long for fear that pieces of our incredible story will start slipping from my memory.

And you know what’s interesting about my decision to write this now? I looked at the calendar and it just so happens that Wednesday this week (in two days) marks 30 weeks out of the womb for you. You only got to be cozy and growing in there for 30 weeks and now you’ve been out for 30 weeks. What odd (and serendipitous) timing.

You’re almost 30 weeks old but you’re supposed to only be 20 weeks old. There’s a constant math equation in our heads when we think about your milestones and development. Having a preemie isn’t as easy as “oh she’s 6 months old so she can now ____”; we are always subtracting time from your age to make sense of where you’re at and how you’re developing.

For the record, you’re perfect.

Picture 1 was taken November 3rd, 2022 at 5 weeks pregnant. Picture 2 was taken January 29th, 2023 at 18 weeks pregnant. Picture 3 was taken the day you came, April 26th, 2023 at 30 weeks pregnant.

I share these pictures to show how my severe preeclampsia progressed. Of course, we didn’t know I had it until 25 weeks gestation when I was diagnosed and hospitalized, but once we were in the hospital it was tough to understand just how swollen I had become due to the disease. When you’re in it daily, you don’t see it. While there were so many other “invisible” symptoms to the outside eye, this was the most “obvious” symptom — and what’s hard, especially as a first-time mom, is that I just thought the swelling I had was a “normal pregnancy thing.” I’ll save everyone the pictures of my excessively swollen feet, but let’s just say — it was scary and totally not normal.

I started taking daily face pictures in the hospital when one of my favorite OBGYN doctors came in to talk to us one morning when my labs had taken a turn for the worse. She kindly said: “I’m not being mean, but you look puffier than normal. Pay attention to your face swelling because I don’t think you looked like this even a week ago.” She also told us that morning — as gently as possible — that she would be surprised if we made it through that week. I was devastated.

We kept having conversations with doctors and nurses about the growth and development milestones you were having each week while still in the womb. Our ultimate goal was to get you to 34 or 35 weeks — coming to terms with you likely arriving more than a month earlier than that felt impossible, especially when we kept hearing even 32 weeks was such an important goal.

The main concern for all of us was your lung development. When I was first admitted and things were quite scary and they weren’t sure how or if I would respond to the medication, they gave me a steroid shot to help your lungs develop quicker. But it only helps for 2 weeks and it had been almost 5 weeks since they gave it. They can also only give it twice. So we asked that same OBGYN what she would do if she were in our situation given my labs going in a downward spiral. She said she would get another steroid shot — so we did.

And thank god we did because you came only 4 days later.

your birthday

When I woke up, the first thing I told the on-site doctor that day (the doctor who delivered you, Dr. Barrett!) was that I felt like I was getting sick — like that shaky, weak feeling you get when you’re coming down with a cold or flu. I remember she put on a mask after I said this (just in case) and told me that she remembered feeling like this toward the end of her pregnancy when she had preeclampsia with her first — that the combination of everything my body was going through with pregnancy, severe preeclampsia, and gestational diabetes in addition to the cocktail of meds I was on (7 different medications: nifedipine and labetalol 2x per day to control blood pressure, insulin 4x per day plus more as needed to control blood sugar, protonix 1x per day to help with crushing epigastric pain, and my other normal vitamins and medications 1x per day) could really wear down my system.

I went on with my normal morning routine, constantly thinking about how much you were (or weren’t) moving. Your movements had significantly slowed down since the weekend prior and I had been keeping my medical team updated because I was quite concerned. A normal day consisted of 2x monitoring you — once in the morning and once in the evening — unless you weren’t meeting the accelerations and decelerations they needed to see. You were always hard to monitor — a little wiggle worm — but over the last several days we had to do additional BPP monitoring with an ultrasound because you weren’t showing us you were stable in there with just the heart rate monitor.

The day before you came, one of my nurses came in to stop me from eating breakfast “just in case” we had to do a c-section that day given all of our monitoring concerns. But… I woke up starving and had already eaten a bar that morning. So she let me eat breakfast and we thankfully didn’t have to deliver that day.

On your birthday, I got up, washed my face, put on some clothes, and ate breakfast. I was so tired. We hooked you up to the heart monitor and I put on some shows and movies on my computer. I was falling in and out of sleep and just remembered feeling absolutely drained and exhausted. We weren’t seeing what we needed to see from you and we had already done 3 BPPs in the days leading up to this day. The nurse told me a fetal monitoring specialist was going to come to speak with me; she said that what she was seeing wasn’t super reassuring and I would need to stay on the monitor until we saw what we needed to see — or until we had to make a call to deliver.

Although I was so upset leading up to that day because everything was pointing in the direction of a very early delivery, a sense of peace came over me after speaking with the specialist. I was simultaneously absolutely terrified and mad at my body for failing us AND I knew that it had worked so hard to get this far and didn’t have any fight left in it.

About halfway through the day, the nurse came in and brought the c-section prep kit and let me know they were cutting off my food intake “just in case.” I called everyone to let them know, including daddy who was on a work trip to Home Depot looking at the cost of building materials 😂

The specialist came in shortly after and still didn’t have a firm decision. So I laid there falling in and out of sleep as they continued to monitor you. Daddy came to the hospital as soon as he was off work and shortly after, about 5pm or so, Dr. Barrett, the specialist, and a handful of labor and delivery nurses came rushing into the room.

The decision was made. You had declared yourself and were coming this evening.

So they started me on a magnesium drip to help prevent strokes and seizures during and after delivery and got everything else prepped. I remember getting emotional as everyone was rushing around and telling daddy and I things about what to expect.

Finally, they wheeled me back to the operating room.

The anesthesiologist started the spinal tap, which is normally a very quick, easy thing, and I kept feeling the needle — meaning it wasn’t quite getting into the right spot. I vividly remember Dr. Barrett standing in front of me looking me in the eyes and holding my hands, reassuring me the whole way through. She made me feel safe, even through my tears.

The team asked me a few times for my name and birthday and read aloud my blood type, to which Dr. Barrett exclaimed, “hey, that’s my birthday and blood type too! It’s meant to be that I’m on call today!” 🤗

The spinal tap still wasn’t working and Dr. Barrett noticed I was going pale white, so they laid me down and tried to do it that way. They sent a nurse out of the room into the hallway — where daddy was waiting — to get a cold wash cloth for my forehead.

Finally, they got the spinal tap to work and I felt an immediate rush of tingles all the way down my body. They laid me down and asked me if I could still feel anything in my torso area and I touched on my left side where I could feel, forcing them to re-sterilize that area (oops 🤪). After a few minutes, everything was numb and daddy was finally able to come in the room.

The c-section simultaneously felt like a blur and like it lasted forever. I mainly remember this odd feeling of tugging throughout the surgery, as well as feeling totally nauseous on and off. The anesthesiologist would give me something every time I felt nauseous that made me feel better — but he also gave daddy a puke bag just in case. The lights on the ceiling were kind of mirrored so I could see the surgeons’ hands working, but not the detail of it.

When they finally delivered you, you let out a tiny cry and my eyes welled up — it was such a good sign that you cried. It meant your lungs were working in at least some capacity. I looked at daddy and said “it’s good, the baby cried” as the NICU team whisked you away.

The surgeons asked daddy if he wanted to announce girl or boy, but neither of us had seen you! Finally, someone said “it’s a girl!” and I remember saying so many times how I couldn’t believe I was right — I had an intuition from early on in our pregnancy you were a girl. What an amazing moment.

We didn’t get our golden hour and I didn’t even get to see you until several hours later, but your birth was still magical. Daddy and I were so happy and relieved that you were here. We were also scared for what your healing journey — and mine — would be like, but we knew we could tackle it together.

When we finally got to go back to the NICU, they had you in your little incubator, on CPAP, and all hooked up to so many monitors. I remember being so nervous to touch you — I didn’t want to do anything that could hurt your fragile, tiny little body.

But I was finally able to touch your little toes and it was the best feeling — you were real and you were really here. I don’t remember how long we were able to stay in the NICU that night, but it wasn’t long enough.

We had a long journey ahead of us, but we would do it as a family. Daddy and I would fight fiercely for you every day during your 7-week NICU stay — but that’s for another blog post and another day.

adeline's nursery

When I think about the memories Adeline will have of her childhood, two things come to mind.

  1. Ben Platt’s song “Childhood Bedroom” — the lyrics are just the sweetest

  2. A story I saw on Instagram of someone a few years older than me saying their parents prioritized fun and playfulness growing up… I love how that’s what she remembers about her childhood

My hope for our girl is that she’ll always feel our love and playfulness every day growing up. That she’ll laugh every day. That she’ll feel free to be who she wants to be and always feel the most at home, at home. I want her to have the best memories of her childhood and can’t wait for all the fun we’re going to have together.

So when I was designing my “office,” which I secretly always knew would become a nursery eventually, even before we were pregnant, I wanted to make it whimsical. And when we found out she was coming into our lives, we didn’t know if she was a girl or boy and it didn’t matter — I just let the fun, playfulness, and whimsy priorities drive design decisions.

So I picked a wallpaper that fit the job well — a William Morris pattern that almost feels like you’re walking into a secret garden. And then I probably looked at 17 different green paint colors to find the perfect fit — and Sheraton Sage made the cut!

I wanted her room to feel elevated like the rest of the house — even if still playful and whimsical — so I followed the same “rules” I use throughout the rest of our home: mix old and new, contemporary and traditional. I love the juxtaposition that brings to design. So I found an antique mirror for above her dresser and mixed modern furniture with traditional wallpapering and trim. I also played with patterns and colors, mixing the floral wallpaper with a geometric rug, and bringing the green, pink, and gold from the wallpaper to life throughout various pieces of the room. You can tell I LOVE color. 💚💗💛

While I of course wanted the nursery to be beautiful, I also wanted it to be functional. So we made space for toys and blankets, found the perfect side table for the rocking chair, hung up a developmentally appropriate mobile, and invested in furniture that will grow with her (a 4-in-1 crib and dresser with removable changing table!). I love the functional furniture especially because although I’d love it if she stayed little forever, I know that’s unfortunately impossible.

Another tip I implemented in this room is shopping our house. While we did get a lot of new items gifted to us or purchased ourselves, we also repurposed some accents we had in other places of our home, like the blanket and toy basket, the basket that’s holding the diapers, the shelf behind the rocking chair, and the faux tree in the corner of her room. And honestly, all of these things look so much better in her room vs. anywhere else we’ve had them before. It just makes sense… love when that happens and things just fall into place.

When I first came home from the hospital without Adeline, I didn’t even want to go into her nursery. It was a sad reminder that we were home without our babe — and that she wouldn’t be home for several weeks or months. (More on my battle with preeclampsia here.) But as she continued to do better and better in the NICU, I felt better and better about spending time in her nursery to pump or just finish final preparations for her to come home. It’s now become my favorite room in our home — and it’s a lesson I’ll always take with me: no matter the room, design a space you WANT to be in.

letters to little liberte: 01

Hi baby,


Tomorrow marks 4 weeks since we were admitted to the hospital. What a whirlwind it’s been. I never thought that we’d be hospitalized at 25 1/2 weeks. I never thought we’d have a normal prenatal appointment on a Tuesday, be sent to do some labs that afternoon because my blood pressure was a bit high, monitor blood pressure at home with it increasing to a concerning rate over the next day, come to the hospital that Thursday for “some monitoring,” and then not be able to go back home for at least 9-10 weeks, until you arrive. I never thought we’d be diagnosed with severe preeclampsia or subsequently with gestational diabetes. I never thought we’d be on the cocktail of medications or the near constant monitoring we’re now on just to make sure we can keep me healthy and you growing strong for as long as possible. I never thought this pregnancy would be a fight for our lives.

We’ve learned a lot since being here. For starters, we’re among only 1-2% of pregnancies that develop severe preeclampsia and have been told by our doctors that it was a “very early” diagnosis, which is concerning as severe preeclampsia can progress at an alarming rate. We’ve also learned that none of this is our fault and that we couldn’t have controlled or changed the outcome no matter how hard we tried. Severe preeclampsia and gestational diabetes are both caused by placental hormones — nothing we could have known or done to change our course. It’s a myth that if we were just “less stressed out” we could have prevented this from happening. We were always meant to go on this journey together. But that doesn’t mean I don’t still question daily why my body has failed us.

While it’s been 4 weeks since we were admitted, I still haven’t found a good routine to keep busy and keep my mind off of all the what ifs and away from the darkness of it all. I have more bad mental health days than good ones, but I’m trying to keep my mind on the end goal — that each day we’re here is a great day. It means you’re still growing healthy and strong and my body is still hanging on and giving you what you need.

The staff are wonderful. Every nurse that’s taken care of me so far is my favorite — and that’s a lot of favorites. I’ve seen at least 17 at this point. Most of the doctors are wonderful too and I found out one of my favorite doctors “claimed” us and will be on call for your delivery — YAY! But even though everyone is wonderful, I still wish I could be home. It’s lonely in this stale hospital room. I miss the warmth and joy of our home — the reading chair in our room, the cozy fireplace, the way the sun comes in through our big windows.

I feel lucky that I’ve never had to experience any major medical trauma before this and haven’t had to stay in a hospital long-term, but now I can say I understand what it means to feel overstimulated and “touched out.” Even though I have a good idea of our daily monitoring routine now, it’s still a lot each day: blood pressure monitoring every 4 hours (yes, through the night as well!), insulin shots 4x/day, blood sugar checks 2 hours after every meal, monitoring you 2x/day for at least 20 minutes (unless you’re not cooperating in which case it could be several hours… you do better every day 😉), a cocktail of meds after breakfast and before bedtime, and then any myriad of other to-dos depending on what’s happening — e.g. this last week we switched from an oral iron supplement to an IV infusion instead so it’d be easier on my stomach.

And that’s just a “normal, uneventful” day. If my blood pressure spikes at or above 160/110 (if either number reaches those maxes), we go on an intervention protocol where blood pressure meds are given through my IV midline, sometimes oral meds are taken as well, you’re put on a monitor, and my blood pressure is checked every 10 minutes for an hour, every 15 minutes for an hour, every 30 minutes for an hour, and then once per hour for 4 hours after that, for a total of 7 hours of monitoring and adjusting meds as needed. I’ve been on protocol at least 5-6x since I’ve been admitted and it doesn’t get any less scary and uncertain. I know for medical professionals it’s probably just standard and normal, but the way things can just change so quickly with this disorder is quite the heavy mental load. The last protocol we went on my blood pressure was the highest it’s been since we were admitted and we had to do 2 rounds of IV medication instead of just 1. I was also in a lot of pain due to another, we think separate issue, so it was freaky all around. Your daddy came last-minute in case we had to deliver you, but we made it through!

I’d be lying if I said I wasn’t afraid of birth. The only thing I want is to meet you, but knowing how unpredictable this disorder is, I’m worried you might have to come too soon or that my body won’t handle the stress of the delivery well. I’ve been reassured that this special care unit we’re in specializes in our issue, but it doesn’t make it less scary. I’ve also been told that we may have to stay for another 6 weeks after delivery if my blood pressures don’t adjust back to normal after delivery. I feel like we’ve already missed out on so much of this pregnancy — I’m not able to finish your nursery, we had to cancel our baby showers, we couldn’t do “normal” maternity photos — I don’t want to spend a second longer than we absolutely have to here, but I also want to make sure both you and I live long, healthy lives.

One thing is for sure — I can’t wait to get our lives started together, and I know your daddy can’t wait for us to come home. We love you little nugget. ❤️