Feeds:
Posts
Comments

Archive for the ‘Zoë’ Category

Remembrance

Happy birthday my dear, sweet Lennox and my beautiful, strong Zoë.

A good friend asked how we would be spending this day.  She wondered if we would do something special to mark the day or if we would carve out quiet moments to remember.  We do a little of both.  It’s a quiet day for us.  A still day.  A day when we feel like we exist outside the rest of the world.  Your daddy and I will have a small birthday treat in your honor. Something sweet to celebrate your birthdays.  The rest of the day we actively remember.  There are 362 days every year when you are never far from our thoughts; your names always drift through my consciousness and memories of you still float out of the depths of my brain daily.  But on your birthday and on your individual special days we let down our guard and we remember.

And, as always, we speak your names.

Love.

Read Full Post »

Zoë’s Day

She was exactly 21 days old, four years ago today.

Had she been born on THIS day four years ago, she would probably still be here.

Sweet Zoë Harper.

Your little sister doesn’t quite understand why I keep scooping her up for hugs and burying my face in her neck today. She’s humoring me with lots of drooly “mwahs” and she didn’t mind sitting in the rocking chair for an hour while I smelled the almond soap in her hair. We looked at the photo of your name in the sand that hangs on her bedroom wall. We played on the playground and had snack. We did all the things you and I never got to do.

Even though you aren’t here, you are always with us.

We miss you.

Read Full Post »

Three years

My dearest Sweet Zoë,

These three years have gone by so fast. I hate to sound clichéd, but it seems like it was just yesterday that we were there with you in the NICU. I can still remember everything, every second so vividly.

I miss you. Every day, I watch your little sister and I think of you. Sometimes, the fact that I have her because I don’t have you hits me so hard it takes my breath away. It is because of you that I remember to take the time to be in the moment with her. Dishes can wait; laundry will still be there later; this minute in her life only comes once. Thank you for making sure I know that. My promise to you is to do my absolute best to gather up as many of those moments as I can and truly be a part of them.

What can I say, Sweet Zoë? I love you. I miss you. I always will.

Read Full Post »

Zoë Day

If there were ever a day I wish I could wipe from the calendar, it’s this one.  This day marks the worst nightmare I’ve ever lived through.  Lennox’s death was hard, but not unexpected.  We’d accepted that his chances of surviving were so small.  Zoë, however, brought us so much hope every single day.  When we rushed into that NICU room two years ago today to see a crowd of nurses and doctors surrounding that little bed, our entire world just slammed into a brick wall.  It never goes away.  It doesn’t fade.  I can still recall perfectly every second, the sound of empty vials of drugs being dropped on the floor, the sight of the neonatologist’s eyes staring at me over his mask, the feel of someone pressing a wet towel against my neck.  I remember feeling too heavy too move and, at the same time, like I’d lost the boundaries of my body and become vapor.

Every morning, I put on my necklace with their names, and they are with me.  In my life, so different from what I thought it would be two years ago, they are with me every day, every hour.  I say their names.  I remember the feel of them in my arms.  I remember holding Zoë against my chest and feeling her tiny fingers grasping against my skin.

Thank you for remembering our Sweet Zoë with us today.

As I did for her brother, I am putting out the request for donations to the March of Dimes.  I can think of no better legacy for Sweet Zoë than working to prevent premature births and to increase the knowledge needed to care for extremely premature infants.  Any size donation is welcome; there are pre-set amounts and an option for a custom amount. Donations may be made anonymously if you prefer not to have your name listed on the web page, and the amount of your donation is not disclosed to anyone.

Read Full Post »

It turns out that the State of Texas instituted advanced metabolic screening on all infants this past January. If I heard the doctor correctly, it actually went into effect on January 3, which would mean that Lennox and Zoë were among the first to benefit from it.  It also means that the doctor didn’t have to go to the lengths he thought he might to try to get Zoë’s blood sample tested for some of the rarer conditions that might have caused her sudden acidosis.

As it turns out, she tested negative for those 25 additional conditions. The cause of death remains, and always will be, extreme prematurity. We’ll never have an explanation for how a little girl who had amazed everyone with how well she was doing, with how many hurdles she cleared suddenly just stops. If you ever wondered why the fund raising is so important to me, why I push so hard for money to be donated to the memorial fund or to the March of Dimes, that’s why. The not knowing. Someday, in some research program, someone will find out what happened and while it won’t help me, it means some other mother will get an answer and will know why on the same day she cheered to hear that her preemie gained that coveted second pound AND got moved to the less critical care room her sweet, beautiful, funny three week old’s heart just suddenly stopped.

So. That’s it. Our final answer. There is some comfort in knowing that it wasn’t something genetic. It was a crap set of circumstances that we could not have predicted or prevented. Some comfort. If we try again and if I get pregnant again, I don’t know how much fear that knowledge will alleviate. Lightening does strike the same place twice, you know. The odds may be against it, but it happens.

But, now we are done with the hospital and the doctors. Almost exactly one week past my due date, I’ve finally deleted the phone numbers for the neonatologist and the NICU from my phone. Another door closes.

Read Full Post »

Crap.  

So, once again, I called Zoë’s doctor to see if the autopsy report was ready. After all, three weeks ago, he told me it would probably be ready in two weeks. But then it was “spring break” as Nurse T put it and lots of the doctors were on vacation.

A brief aside here…
I HATE talking to people. I’m beyond non-confrontational. It doesn’t matter that I’m entitled to that report. Every time I pick up the phone I feel like I should leave a message apologizing for bothering him.

Normally when I call, I just get the answering machine. That suits me just fine. I leave practically the same message each time (I have to rehearse phone calls like this in my head): “This is Allison Simpson. I’m calling to see if my daughter, Zoë’s autopsy report is ready. yada yada yada phone number call anytime yada yada yada. Thank you.” Today, I realized how long it had been and put on my big girl pants and called. Only I got his secretary. Yikes! A real person throws a spanner into the finely tuned works of my prepared speech. Particularly when she keeps trying to cough up her spleen in my ear.

However, she did think she’d seen the report come in. She was going to page the doctor and double check. That means we will get to hear the final report, either tonight or perhaps sometime this weekend. I’m not sure I’m actually ready for that. I mean, yes, I want to know. I need to know. That the nurses and doctors were as confused as we were has driven me, us, crazy. On the other hand, do I really want to know? What if the answer is “We have no idea?” or “Well, there was this rare genetic disorder…”? How do we go forward from there? How do we try again with THAT hanging over our heads? What if the answer is something that could have been avoided?

I swear, I think I can literally feel my digestive system tying itself in knots. I’ve never been anticipating AND dreading a phone call simultaneously like this before.

Read Full Post »

Before Zoë died, I was planning to write a day in the life of a NICU parent post.  I wanted to have a detailed chronicle of what our day was like.  Then the train derailed and it never got written.  Now, before I lose that memory I need to get it down.

The alarm went off at 6am each morning so I could pump. We’d just gotten the system down. During the night, I pumped at midnight, four, and six for 20 minutes (the nap timer on my alarm clock goes in 10 minute intervals and since I dozed off while pumping, I had to set the alarm). Before bed each night, Shannon put a large ziploc back with three sets of pumping accessories next to the bed. My hands-free pumping band and the cloth diaper Zoë had slept on were between my pillow and the alarm clock. I had a full mug of water (as much as I hated everything about being in the hospital, those big plastic mugs with the straw and the snap-on top are the greatest) handy as well. The alarm would go off, I’d get propped up against the headboard, wrap the band around me, hook up the pump parts, turn it on, set the alarm, make myself drink the water, put the cloth diaper over my face, and exist in some sort of alternate place until the alarm went off again. Then, I’d nudge Shannon awake. His job throughout the night was to take the bottles, put the correct time on the labels, put them in the refrigerator, and put the dirty pump parts in soapy water to soak. We’d shower, dress, grab some breakfast, bundle up against the cold, and head out into the barely light morning to drive the 12 miles to the hospital. We took the camera with us every day and an insulated lunchbox with the bottles of milk I’d pumped since we saw her the night before. While others rushed down the highway on their way to work, we rushed to see how our little girl had faired during the night.

Parking at the hospital was a nightmare. We got good at our system though…Shannon would drive, navigating the tiers of the parking deck while I looked ahead, checking both the up and down ramps to find a space within easy walking distance of the elevator. I still had a hard time walking far uphill, so we needed to be close. A quick elevator ride, a dash across the street through the freezing wind that roared in the tunnel created by parking deck and various hospital wings, a quick spin through the revolving door. The walk through the lobby, past the line of nurses and doctors at the coffee stand, around the corner and through the hallway under construction to the elevators. A short ride to the first floor. Some mornings, the waiting room outside the elevator was full of families, waiting vigil outside the labor and delivery ward. Some mornings it was empty. We were usually there early enough that the NICU waiting room was empty and there were only a couple of mornings that we had to wait because someone was being admitted and the NICU was closed to visitors. Almost all of the secretaries knew us by sight, so we rarely had to say, “Simpson, Room 4B.” The secretary would call back to make sure it was ok for us to come in as we filled out our nametags, then she’d buzz us into the scrub room. Coats, scarves, gloves all got shoved into a locker, cell phones got turned off, the camera barely fit into Shannon’s jeans pocket. Set the timer on the wall, get a handful of the harsh surgical soap and start the first half of the three minute scrub. The water in the sink was either steaming hot or freezing cold…foot pedals turned on one or the other but there was no way to mix both. We got very good at turning on the hot and rinsing off as much soap as possible before it got unbearable, then switching to the cold water and finishing up before it got untolerably cold. Re-soap and repeat for another 90 seconds. Grab the lunchbox with the milk, all carefully labelled with her name, the medications I was taking, the time and date it was pumped and my initials. Ignore the fact that your nose itches so you don’t have to wash your hands again. Around the corner, through the door, down the hall past the rooms where some parents stay overnight, past the “resource room” where we spent that last hour with Lennox, around another corner, down another hall. A quick glance at the board to see who our nurse is for the shift. Down another short hall, fighting the urge to glance in Room 4A where Lennox’s bed had been. Funny how quickly that became a natural instinct to look. Now it was close to 8:45. Round the corner and see her bed with the giraffe cover over it. If we knew the nurse, she’d start giving us the update…how much she weighed that morning, how many times she’d pooped. Had they increased her milk that day? Did she have an x-ray this morning? What were her blood gasses? If we didn’t know the nurse, we had to show our wrist bands first to prove we belonged. We’d hand over the milk, the nurse would initial the bottles and they’d either go into the refrigerator in the room for use that day or in the walk-in freezer down the hall. A quick “wash” with alcohol gel and I’d open the portholes on the incubator to touch Zoë. Adjust her hat or her eye shade, put a hand on her back, talk to her. I’d sit in a chair by her bed while Shannon took photos and talked to her. Then, I’d reluctantly let him take a turn sitting next to her, but only for a short while. We’d watch her heart rate and pulse ox on the monitor. Shannon became really good at reading the respirator monitor as well, watching when she fought against the respirator or was breathing over it. He’d questioned the respiratory tech about every number on that machine, what it meant, what it did for her, what we wanted to see, when and why it might be changed, what each alarm indicated. We knew what each tube was for and how they were used.

We usually stayed until about 9:30. If the doctor was there and doing rounds, he’d stop and talk to us, letting us know how she was doing and if he had any concerns or if there were any tests/procedures planned for her. Reluctantly, we’d give her one last “hug,” tell her we loved her, wish the nurse a quiet shift, and leave. On good days, we chatted happily about how well she was doing, how good her color was, laughing about her silly faces, her diva-crankiness. On bad days, we dragged our feet, wishing we could stay with her, wondering why this had to happen, hating that we couldn’t make it better. On the drive home, the grandparents were called and given the daily report.

We’d get home around 10. Shannon would start work, while I pumped and had a snack. Work, pump, eat, work, pump, nap. I pumped every two hours when I was awake. The whole process, from getting the pump set up to getting the bottles in the refrigerator and the parts cleaned took about 45 minutes, with the actual pumping taking 20-30 minutes. I took a nap most afternoons while Shannon finished up his work day. We’d eat a quick dinner if we had the time, then by 7 we were back in the car, in the cold and dark, to head back downtown. Evenings tended to be more crowded, both in the L&D waiting room and in the NICU waiting room. More often we found ourselves sitting there doing sudoku puzzles, trying to ignore the reality show blaring on the television, until we could finally go back. Sometimes, I’d have to ask to be allowed in to pump (after the first few visits of having to go home sooner than we liked because I was in pain, I always brought my pump parts with me). On the nights when we didn’t wait, we’d have a repeat of the morning…scrub, get update, greet Zoë…then I’d go pump briefly while Shannon got some Daddy time. When I came back, we’d turn over the day’s bottles to the nurse and I’d get my turn in the chair. Later on in her stay, I started bringing her stories to read. I’d sit with the porthole open, my head pressed against the side of the bed, one hand on her back, one hand holding the book, reading while Shannon turned the pages for me. I read her books that had been mine when I was little. We’d say her name over and over, reminding her to breathe, to calm down, to let the machine do it’s work when her stats got out of whack. I liked the night visits best. There were rarely other people in there…just a few parents, mostly moms who were still patients…the nurses seemed more relaxed, able to spend time and let us really BE with Zoë.

We’d stay until 9:30 or so, then wish Zoë sweet dreams, again offer the nurse our hopes for a quiet night, and regretfully leave. On our way out the door, we’d fill my bag with my pump parts with more bottles from the cabinet. I was going through dozens a day. We’d go home and eat dinner if we hadn’t before we left, get the pump parts ready, and collapse into bed to start all over again.

Read Full Post »

New photos

There are some new photos posted over on Sweet Zoë.

Read Full Post »

3:30pm 01-24-08

I don’t have any words left.

My Zoë died this afternoon.

We don’t know why yet.

My Zoë is gone and my Lennox is gone and I don’t know if anything will ever fill this hole.

Read Full Post »

Read Full Post »

Older Posts »

Design a site like this with WordPress.com
Get started