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When
Kate, a 29-year-old mom outside Boston, who has had countless miscarriages, found out she was pregnant with
a second daughter, she became elated. But at 36 weeks along, she got a news worst than a nightmare: Her baby had two brain malformations. Kate decided to terminate the baby and eventually found solace in a support group on the
website Ending a Wanted Pregnancy. Read the story she share with Yahoo Parenting.
My husband and I always wanted a big family. We wanted to have a lot of kids and to start young and have them close together. In 2010, we had our first. A healthy baby girl. But when we were ready for number two, getting pregnant — or, rather, staying pregnant — was harder. I had three miscarriages before a pregnancy finally stuck. I was expecting a second little girl in the summer of 2012, and everyone around me said everything looked great.
Well,
almost everyone. At my 18-week fetal scan, a technician thought she saw
something – she wasn’t sure what, exactly — so they sent me for a Level
2 ultrasound at a local teaching hospital. “Level 2” meant that it
would be more detailed than the standard sonogram, and a maternal fetal
medicine (MFM) specialist would look at it. When I went for that test,
the MFM specialist said the baby was healthy. I was worried, but when I
expressed my concern to the hospital’s genetic counselor, she said, “His
job is on the line. He must be completely confident.”
That whole pregnancy was hard for me. I was sick for much longer than most people are. I had sleep apnea. When I was pregnant with my first daughter, she would kick responsively, and then she would take naps. It seemed logical. This baby never stopped moving, but she never did anything responsive, either. The movements were so random. I remember telling a friend, “This baby is already different than my first.” I don’t know if it was that, or my history of miscarriages, or having that seed planted that something might be wrong, but I was uneasy.
Because of that worry, at 35 weeks, my midwife sent me for a “peace of mind” ultrasound. I was eight months pregnant — huge! — and I went to the hospital thinking I was being silly. The rational side of me knew everything was fine. I figured they would tell me all was good, put my mind at ease, give me a picture and send me home.
I went to the appointment alone, on a Wednesday in May. I was so chatty with the technician while I was lying on the table. Towards the end, I said to her, “It’s funny, I keep picturing the baby I already have, but I know this one will be different.” And she looked right at me, with these serious eyes, and said, “This baby will be different. They are all different.”
While I waited for the doctor, I worked on the sweater I was knitting for my little girl. When two doctors came in, one of them asked me about it. Was I making it for the baby? I told her I was, and, with tears in her eyes, she said, “It’s beautiful.”
Then she continued. “The things they couldn’t find the last time you were here, we are seeing those things today. Your baby has brain malformation.” Right away, she said, “We might be able to arrange an abortion, we just don’t know. We can arrange an adoption if that’s what you want.”
I’m grateful that she led with that. It told me it was safe to talk to her about options, and it told me that something was very wrong. That was the only thing she said that got through to me. Everything else came up against that denial wall. Of course, she told me about keeping the baby, too.
I
know she said the words “Dandy-Walker,” which I know now is a brain
syndrome that has varying degrees of severity. I remember asking, “Are
babies with this ever normal?” and she said that sometimes they were.
She told me they couldn’t know the severity of the situation until after
I had an MRI. That’s how they would determine if my baby would be OK or
if she would be “incompatible with life.” Those are the words they
used. Incompatible with life.
I
was in total shock. I wasn’t even crying. I picked up the phone to call
my husband, and all at once, I completely fell apart. By the time he
got to the phone, I was unintelligible. “Where are you?” he said. I
named the hospital and he said, “I’m on my way.”
We were in crisis, and in crisis, you don’t talk very much. You say what you need to say, and the rest is just thoughts turning around in your head constantly. My husband was wonderful. I would cry until I didn’t have any tears, and he would pick me up and carry me to our room. I knit and knit and knit. I knit in my worry and knit in my fear, and I finished the sweater. I wove in the ends, and then my husband and I got in the car and drove to the MRI.
It
was a morning appointment, and at the end of that day we met with the
neurologist, who told us that our baby had Dandy-Walker malformation,
the most severe presentation of the syndrome. It basically meant there
were holes in her brain. She also had agenesis of the corpus callosum,
which meant the bridge between the two hemispheres of her brain didn’t
grow. So we had two malformations, each of which had a wide range of
outcomes, but, combined, had a horrible prognosis. The doctor said, “We
expect your baby to have moderate to severe mental retardation; she’s
going to have moderate to severe physical disability; she is probably
never going to walk or talk; she will possibly never be able to lift her
head; she is going to have seizures all of the time.” At first, I was
thinking, “This doesn’t make sense, she’s always moving,” and then he
mentioned seizures, and I understood.
In
that moment, I had to shift my thinking. I was hoping for special ed,
and had been focusing on questions like: How much should you save to
know your special-needs daughter will be OK after you die? I was
thinking about long-term care and mild to moderate disability. Instead, I
had to think about a baby who was probably not going to live very long,
and the longer she lived, the more pain she would be in. That
realization – that I was more scared of her living than of her dying —
is what made the choice for me.
When
it comes to a decision like this, there is no good option. What you
want is a happy, healthy baby. The doctor asked if we had any questions,
and I said, “What does a baby like this do? Does she just sleep all
day?” The doctor looked so uncomfortable. He said, “Babies like this one
are not generally comfortable enough to sleep.” That’s when we thanked
him and left.
On the way home,
even though I knew what I wanted to do, I couldn’t say the word. What
kind of mother is eight months pregnant and wants an abortion? I turned
to my husband and said, “Tell me what you think we should do.” He said,
“Kate, you do not have to do this, but I think we should ask about the
abortion.”
It was a gift. It
felt like light and fresh air. I had been feeling so dark and so
trapped, and when I realized we were together on this, I felt free. I
knew what to do. It didn’t matter anymore that people were going to call
me a murderer, or that I’d never heard of anyone doing this. It didn’t
matter that we didn’t even know if it was legal. If I had my husband, I
could do this.
I
called my doctor as soon as I got home. While we were waiting for her
to call back, I didn’t know if we had a safe and legal option. I
remember thinking, “If we can’t get the abortion, I’m going to run away
somewhere rural and I’m going to have this baby by myself and let her
die without intervention.” That would have been so dangerous, and I
could be dead right now. She was a high-risk birth, not a regular
healthy birth. Her head could have swollen with fluid at any time. Even
if it went smoothly, and I had my baby and she had died in a few hours, I
could have been put under investigation. The risks that I was willing
to take to let this baby go in peace, in the way I believed she deserved
— it’s terrifying. But I was desperate, and I was so untrusting. I was
scared the police would get called on me for just having these thoughts.
My
doctor called back at 6:30 that night. It was a Friday, and my husband
and I were out for a walk when the phone rang. Immediately, the doctor
said, “I am so sorry, but if you want the abortion you need to call
before 7 pm, which is the end of the workweek Mountain Time, because the
clinic closes for the week in a half an hour. And you have to be on a
plane to Colorado on Monday.” We were in Boston, where there are a
million medical schools and hospitals, but the only doctor in the
country who would perform this late an abortion was in Colorado.
(Actually, there was one other, but that clinic was closed for the
week.) My doctor barely had time to explain everything, she just said
I’d have to be in the clinic on Tuesday. It was a four-day procedure,
and I had to have it done by Friday, when I would be 36 weeks pregnant.
There is no doctor in the country who performs abortions after 36 weeks.
Then
she added, “You have to show up with $25,000.” We didn’t have $25,000
sitting around. We are a middle-class family. We don’t have that kind of
credit, either. But it didn’t matter. I would figure it out.
So
I called the Boulder Abortion Clinic in Colorado. We scheduled
everything we needed to, but then I had to get money. I called my
parents. I told my mom everything, and when I told her I wanted to get
the abortion, she said, “That is what I would do, too.”
It
was such a relief to hear those words. It’s one thing to get an
abortion, it’s another thing to get an abortion at eight months. I felt
like such an outcast. It’s so heavily tabooed that I was afraid to even
tell my mother. But once I knew I had her support, I blurted out, “I
need money.” My parents took it out of their retirement fund, which is
probably what we would have done if we’d had more time. But you can’t do
much with no business days.
On
Monday, we flew to Colorado. I made up a story that I was six months
pregnant with twins, in case someone tried to stop me from getting on
the plane. I was so afraid that I was going to be found out, that
someone was going to get in the way of me getting to the clinic.
The
whole first day was counseling and testing to make sure it was safe to
do the procedure. They want to make sure you completely understand what
is going to happen and that no one is pressuring you into the decision.
At the end of the day, I signed all the paperwork, and the doctor
injected the baby with a drug that, over a few hours, slowed her heart
to still. It was a very, very difficult day. Euthanizing the baby is,
obviously, a very hard thing to do. After the injection, he asked how I
was feeling, and I just said, “I feel so sad. I’m going to miss her.”
My
husband and I went back to the hotel and I lay down until she stopped
moving. I could tell when she was gone. It feels very different. The
second and third days were short appointments, so we took a nice drive
through the Rockies to pass the time. Then on the fourth day, they
induced my labor. I got Pitocin, and it was actually a very natural
birth. It was quite healing for me. I couldn’t do anything for this baby
— I couldn’t fix her brain or make her well, but I could deliver her
from my body. I chose to view her, so they cleaned her up and brought
her in and she looked a lot like my older daughter. She was beautiful
and she was whole. I got her footprints and had her cremated and they
sent us her ashes in the mail a few days later. We wanted to name her
after a flower, so we called her Rose.
Ten days after we had that 35-week ultrasound, she was gone.
Late
in my pregnancy, my older daughter would say, “Mama do you have a baby
in your belly?” and I would say, “Yes honey! Want to give her a kiss?”
After I got home, I knew she would ask, so I waited for that moment.
When it came, my daughter put her hand on my stomach and said it: “Mama,
do you have a baby in your belly?” And I said, “No, honey. Baby died.
Baby’s all gone.”
She cried, but probably because I had spoiled
the game. My daughter asked me every day for two weeks. Now, every six
months or so, we talk about it again — her understanding of it evolves
as she grows. At this point, she knows the baby died because she was
sick in a way the doctors couldn’t fix, because she had holes in her
brain, and you need your whole brain to be healthy.My 30th birthday party was scheduled for the Sunday after we got home — two days after I gave birth to Rose. It was only for close family and friends, so I decided not to cancel. I told people that the baby died and that we induced a stillbirth. I didn’t tell them I went to Colorado. I didn’t tell them the baby died because we gave her an injection. But eventually, I told my best friend, and she was wonderful. And that helped me tell other people and speak publicly. My husband is a private person, and he would rather I didn’t tell anyone, but I have healed a lot from sharing and receiving support.
I’ve
gone on to have another healthy little girl, who is 16 months. The MFM
specialist I saw for my third pregnancy said that if it had been him, he
would have caught Rose’s condition sooner. I have explored the
possibility of a medical malpractice suit, but in the end I decided
against it. I decided that I can live in a world where people make
honest mistakes.
My third
pregnancy was hard, emotionally, but today I have a 5-year-old and a
1-year-old. I don’t know about the future — I refuse to make a decision
right now. I’m still healing. But I have two living children, and I had
another baby, whom I still love every day.
Yahoo Parenting
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