Select Page

Due Date

Today is when our baby was due.

Today is when we would’ve met our child and become parents.

It’s hard writing those words, but even harder thinking about what they actually mean. We never knew if our baby was a boy or a girl, though we’re convinced our little one was a tiny princess. We named her, though only we know her name. I try to look at our faces all the time and imagine what she would’ve looked like. There is an emptiness in my heart knowing our family isn’t complete, that there’s someone missing.

I posed a question to people a while ago. I asked if they would consider someone a mother if their child never made it into their arms, and as would you expect, the answers were divided. I’m half in the park that “I am a mother,” and half in the “I’m not” as well. Without having her here in my arms, I feel like I don’t deserve the title of ‘mother,’ but I can’t deny she was here, even if only for a short time.

Her initials are CG, and I wish I could tell you her name, but somehow it doesn’t feel right. I’m tired of her being our secret though, and I want the world to know I should have a daughter here. I’m angry, frustrated, and hurt. I want people to know about her, I want others to miss her, I want others to care.

Today, I should be a mother, holding our little angel, breathing her in and going over all of her little features with the awe only a new mother can have.

Today is a lot harder than I thought it would be.

Say Hello, Wave Goodbye

Even now, nine years after the fact, I struggle about where to post this. I’ve been told so many times that I had a miscarriage, that Maggie wasn’t even a viable baby.

She was my baby. She was my daughter. I held her in my arms, and I gave her a name.

I have a daughter.

Some people I know are surprised to hear this, since I only talk about my sons, Big and Little G. I don’t talk a lot about the fact that there were pregnancies #4 and 5.

I’m going to pull a lot of this from a story I posted at the Preeclampsia Foundation back in 2002. The women in the forums there saved my sanity, and I love them for it.

About 17 weeks into my second pregnancy (my first ended with a miscarriage at 14 weeks), I experienced a day where I threw up all day long. I hadn’t had morning sickness at all, so I was a little concerned, but Car (my husband) and I assumed I had a 24-hour bug. The next day I didn’t throw up, but I simply didn’t feel well. I had a general feeling of unwellness from then on, but nothing specific.

At about 17.5 weeks, the pain started. At first I assumed the pain, which was located just below my sternum, was heartburn. I’d never had heartburn, but I couldn’t imagine what else the stabbing pain could be, and everyone knows that pregnant women get terrible heartburn. The pain got progressively worse until I could no longer work. I asked a few people if this was really what heartburn was like, and they assured me that pregnancy heartburn could be really bad. I took the maximum amount of antacids allowed, but nothing helped.

I had my usual appointment with my perinatologist on a Wednesday, and I mentioned the pain. He suggested Pepcid AC. My urine showed only a trace of protein, so there was no cause for concern, despite the fact that I had to have a friend drive me to my appointment because the pain was so intense.

That evening, as I curled up in a ball on the couch and sobbed, Car decided I needed to go to the emergency room. I refused, positive the ER personnel would laugh at the pregnant woman who couldn’t handle simple heartburn. We finally struck a compromise–I would page my local OB and if she thought I needed to go to the ER, I would. When my doctor returned the page, I was crying too hard to speak with her, so my husband filled her in. She also thought it was most likely heartburn, but said if the pain was bad enough that I couldn’t talk on the phone, the ER wouldn’t be a bad idea.

The first thing the doctor at the ER did was give me something he called a “GI Cocktail.” It’s a lovely little drink that numbs your entire digestive tract down to your stomach, and will apparently subdue even the worst heartburn. It made my tongue and throat numb, but did nothing for the pain. The doctor said, “I don’t know what’s wrong with you, but it’s not heartburn.” They gave me a shot of Demerol for the pain and ran  several tests (blood work, ultrasound, CT scan). After about 4 hours in the ER, all they could come up with was, “We can’t find anything wrong except for some elevated liver enzymes. We think it’s probably your gallbladder. Call your doctor in the morning.” They discharged me and sent me home.

The next day I called my doctor and told her I had elevated liver enzymes and the ER doctor thought I had something wrong with my gallbladder. My wonderful doctor, whom I credit with saving my life, said, “That doesn’t sound right. Let me makes some calls and call you back.” Within 30 minutes, she called me back and told me to go to the hospital for further testing.

From that point on, things become a blur. I was admitted to the hospital on Thursday and put on a morphine drip for pain. My liver enzymes skyrocketed, my platelets dropped. We were told that the best-case scenario was hepatitis. My red blood cells started to self-destruct and my kidneys began to shut down. My brother flew out from Minnesota in case he had to say goodbye. Every possible liver disease was tested for and ruled out between Thursday and Saturday, when the doctors finally settled on the final diagnosis–HELLP Syndrome. They told us that to save my life we would need to terminate the pregnancy. I begged them to prolong the pregnancy long enough to save my child. The doctor told me, “I don’t think you understand. It’s not an either/or situation. If we don’t end the pregnancy, both you AND your baby will die.”

I was 19 weeks pregnant.

On Saturday night a doctor started the process of manual dilation (which is every bit as painful as it sounds), and on Sunday I delivered a perfectly formed little girl, Margaret Marie. Maggie weighed 3.88 ounces and never took a breath on this earth. I held her in my arms, counted her fingers and toes, and decided she looked like my husband, who was weeping by my side.

About six months after Maggie was born, we decided to try again. I miscarried at six weeks. I told myself , “At least it happened early,” but I was still devastated.

Three months after that, I had my first drink.

Not All Anniversaries Are Happy

{sigh} Yesterday was the 6 month anniversary of Robert’s death ~ he was 14 1/2 months old when he died. The past 6 months seem more like a year. I thought time dragged on when my husband Joe was deployed in Iraq, but that flew by in comparison to this. Not a day goes by that I don’t think to myself “Oh no, I forgot Robert at home.”

Or I look in the backseat of the truck & my heart stops because I think “I lost Robert in the store!!!”

Then I realize that he’s gone.

I flash back to the moment I found him laying so still in his crib, I knew in my heart he was already gone. There was nothing I could do.

6 months ago was the hardest day of my life.

Harder than saying goodbye to my husband while I was 9 months pregnant as he drove off on a bus late at night to get on a plane to go to war.

Harder than the day I had to go to the hospital, alone, straight from my OB appointment because they couldn’t find Robert’s heart beat.

Harder than the day Robert was born and the phone connection Joe was on in Iraq sucked and I couldn’t hear him half the time.

Harder than giving birth to Robert, without an epidural because he came so quick it didn’t take.

Harder than the 9 months I was home alone with 3 kids and a husband who was at war and having near misses at death almost everyday.

At 7:55 am on Sunday December 14, 2008 I went to get Robert up and ready for church. I picked my baby up out of his crib and I knew he was dead. I wanted to scream, but I couldn’t. Brianna was in our bedroom watching Playhouse Disney. She couldn’t know what was happening. I carried Robert into the living room, called 911 and pleaded for help.

I gave my baby CPR, knowing it was useless, waiting for what seemed like hours for the police to arrive, it was barely 3 minutes.

I handed Robert to the first officer through the door who actually was in Joe’s unit. He took Robert and another officer and paramedics came in. They tried to work on him, but I knew from the words they were saying it was too late. As soon as I had handed Robert to them I called Joe’s cell phone. He didn’t answer and I didn’t know where he was.

He had left at 4:45 am to take Kameryn to his hockey game. Joe’s phone was ringing, but then I realized, that I didn’t know what to say. I handed my phone over to another officer and said, “I can’t tell my husband. You have to talk to him.” I don’t know what he said, but thank God Joe was only around the corner. Joe barreled through the front door to find me sitting on the floor, sobbing.

Joe called his family to come over and they were at my house within minutes. I couldn’t get in touch with my parents, but finally, my best friend Heather and the police went to my parents’ house to tell them.

All I wanted was to get to the hospital to be with Robert but I had to answer questions. Joe called his LT at work, his 1Sgt from the unit. “God, we need to get to the hospital. Why are we still here?” was that all I could think.

Finally, they let us leave for the hospital.

They took us into a waiting room where we had to wait while person after person from the hospital and police talked to us. Thankfully, not long after we got to the hospital so did numerous people from Joe’s unit, our church, and people from Joe’s work. I was so overwhelmed by how many people came to help us. Much of the rest of the day at the hospital is still a blur. I remember pits and pieces of those hours but mainly I just remember being numb.

My Robert was dead.

What had happened? All the questions the coroner was asking me, that I had to tell the detective the same things I had told the police at the house, I just wanted to see my baby. “When can I see Robert?”

Finally, Joe & I could see him. Our sweet baby boy. All I wanted to do was lay next to him, my head next to him, smelling his hair. Bubby had the best hair, he was supposed to get a hair cut on Friday. I just rubbed his hair with one hand & held Joe’s with the other. Kissing my baby’s head, tears wetting it.

That is how I spent the day 6 months ago

Brothers Forever, Twins No More

We thought we were in a dream, all the joys and fears at the same time. We got two cribs, two sets of every outfit (but in different colors), two swings, two of everything…except two identical boys.

We lost Jonathan James when he was 7 months (in utero). I was given the choice, but I never held him. I had to carry his identical brother Lewis Jordan, for an additional 7 weeks. He just was not ready to leave his brother until then. We knew about the extreme risks of twin-to-twin transfusion, how our surviving son would likely have severe brain damage as blood shunting causes terrible problems for a developing baby. We prepared ourselves for the very real possibility that our surviving son might not recognizing us, speak or walk.

We were destroyed.

I spent the next 7 weeks in a rocking chair in the nursery with TWO of everything; rubbing baby lotion on my hands and inhaling, trying to stop the sobs and the unearthly sounding wails that came from deep within my heart.

But I had another to worry about. Lewis. During all this turmoil, the grief over Jonathan could not be allowed to hobble me too badly, I could not let it, I had to be ready to care for the child that was alive and waiting to meet his parents.

Thank Christ the doctors were wrong about Lewis’ challenges. He was born by C-section on a cold January day, crying out when they removed him from his space. I know he cried out because they were taking him from his beloved brother, Jonathan. They thought it was because he was cold and the lights were bright. Fools.

His kidneys began to shut down 3 minutes after he was born. As they whisked him away from me, I demanded my husband leave my side and go with our son, to protect him, and promise to bring him back to me, healthy and safe.

The OB asked me if I wanted to see Jonathan, warning me that the body’s natural reaction is reabsorbtion, I asked only one question, “are you sure they were identical?” The doctor replied, “one sac, one placenta.” I replied with a heavy heart while still wide open on the operating table, “no, I already know what he looks like, just like his brother.”

Two hours later, my husband brought back our son, placed him in my arms and kissed my forehead. The doctors had stabilized him, no further medical issues had arisen and today he is a healthy, happy, wickedly intelligent nine-year old boy.

I will forever be happy that our son is healthy.

I also will be forever crushed that he does not have his twin brother.

I wish I could make the ache go away.

I wish that I was not jealous of other twins.

I will always wish that I had been strong enough to bring both of my sons into this world (though I followed every order from the medical establishment, I will always blame myself).

I wish I had my Jonathan.

A Rock In Your Shoe

A little while after Charlie died, a girl I volunteered with at the Ronald McDonald House shared her idea with me about the grieving process. She had lost her 5 year old to Cancer a few years earlier so she had experience and was already a member of the “Moms of Angels” club.

She said grieving was much like a rock in your shoe.

And you can’t get it out. Can’t take the shoe off and shake it out. It is there and always will be.

At first it cuts into your heel and ball of your foot causing you to bleed and be in pain. Then after a little while, you can wiggle it around and get it into a spot where you can’t feel it too much.

But every now and then something will happen and make that rock get under the heel of your foot – causing you to bleed and be in pain. So you go through life with this rock in your shoe that sometimes causes you a lot of pain and sometimes is just “there”.

I thought that was very interesting at the time. And now I know that it is very true.

I attended a visitation for a friend’s stepdad about 5 years later at the funeral home where Charlie was. I remember our visitation almost too vividly. I remember greeting hundreds of people (seriously, like 500) – local friends and friends who had driven several hours or had flown in for our 24-day old baby’s funeral. It was very humbling. I had been in that room for various visitations over the last 5 years with very little pain. But tonight for some reason when I walked in the room, I felt physically ill. Like I might throw up. I remember feeling that way the first time I went in the church where we had his service (my home church) and that morning they just happened to have a baptism and sang “Jesus Loves Me”. Again, I felt physically ill.

You never know what is going to trigger one of those “Moments” and the moment might not make you cry and get all emotional or anything, but it puts a knot in your stomach and makes your hands shake and just makes you feel that rock in your shoe.

But I’ll be able to wiggle it back out of the way and go for a little while until it decides to get under my heel again. This is how we are able to go on.

Blindsided

Ever since 2000 when our daughter Elli was born with life-threatening heart defects and nearly died three times the first three weeks of her life, I’ve experienced blindsides.

I wish I referred to the movie.

Blindsides are swift and completely unexpected emotional breakdowns, often experienced when sharing your story with a stranger or a group of strangers.

As the parent of a child with special needs, I have shared Elli’s story countless times with medical personnel, school staff, new acquaintances, and random strangers we’d meet out in the community. I have had the opportunity to share our story for some college classes for special ed teachers and therapists, and for potential donors to our hospital.

I never know how those presentations would go. Will a blindside slam me into a teary mush pile this time? Or will I be able to communicate clearly and strongly?

When Elli passed away a year and a half ago, the blindsides changed. They began striking at any time, in any place, doing anything or nothing at all.

Anything.

A wisp of a memory… her sister’s laugh that sounds exactly like hers.

A glimpse of a familiar-but-no-longer-visited place… driving past her aquatic therapy pool.

The scent of the hospital’s blanket warmer, so comforting after yet another general anesthesia.

The discovery of a long-buried personal item… her bath towel.

Anywhere.

…sitting at the piano in church on Sunday.

…driving down the highway.

…laying in bed, drifting off to sleep.

…watching a movie with my husband.

…waiting for my son’s school bus.

At first, they assailed me daily, even hourly. With time, less frequent and more unexpected… except in the fall near the anniversary of her death and in the winter near her birthday. Those are memory minefields.

At first, the pain was bitter, cutting deeply, exposing raw wounds. Now it’s more of a wistful dull ache, a pain of long separation, hidden under scar tissue and wrapped in hope of heaven one day.

Have you seen me? The random weeping girl in front of the yogurt at the grocery store? If you do, would you spare a tissue? I promise, if I run into you, eyes red, face puffy, I’ll dig one out for you.

Where’s the craziest place you’ve ever been blindsided? What helps you get through it?