- Tuesday, January 06, 2015
- 0 Thank You For Visiting
You Didn't Even Know Her,
How Could You Possibly Miss Her?
I wish you could remember her with me-
what does it take away from your life?
An uncomfortable feeling that you can walk away from,
when you choose?
But you can't, and I understand.
Her body makes you cave and it reminds you of where you came from.
Her small self took up so little space in this space.
My remembering takes up so little space in the world.
If you do not want to remember her with me- please leave me to miss her myself.
My remembering takes up so little space in the world.
If you do not want to remember her with me- please leave me to miss her myself.
It's Been Four Years Now,
It's time to let go
You never held her- her tiny hands were so graceful.
Because you did not hold her, you can not possibly understand how difficult it was to let her go.
When you say "move on", you really mean- be the who that you were before she came.
When you have touched something so precious,
so beautiful-
you can never be who you were before.
I Know That You Don't Understand Right Now,
But This Is All Part Of God's Plan
A most pervasive myth.
Death was never part of God's plan-
never.
She is so very beautiful.
I have a finite amount of time and energy in this world-
not nearly enough time to illustrate
why I will always be changed.
Why I will never stop missing her.
Why I will never get over her-
whether it's been four or forty years.
Why I will never believe that it's
part of God's plan that my daughter died.
And-
as long as I'm here and she's there,
I will tell the world about her.
- Wednesday, December 17, 2014
- 5 Thank You For Visiting
I saved my sleep for later, wanting to sit alone while the new day began.
She would be four today.
- Saturday, December 13, 2014
- 1 Thank You For Visiting
I read this today.
God bless Live Action, and Life Site news, and all of the other groups who work tirelessly to fight for the rights of the unborn every day.
But- this article?
Not only is it scientifically inaccurate (I'll get to that later) but it doesn't matter if this was divine intervention or a misdiagnosis.
While I was pregnant with Beatrix, a number of people came to me with stories about how they knew someone who had received a poor prenatal diagnosis, but who went on to have a perfectly healthy baby.
The implication here was, I should hold on because my physicians may be wrong. My daughter may live -- in fact, maybe all of those things which showed up in the countless tests we had performed were not really there.
The organs growing outside of her body.
Her mangled spine.
Her too large head.
God bless Live Action, and Life Site news, and all of the other groups who work tirelessly to fight for the rights of the unborn every day.
But- this article?
Not only is it scientifically inaccurate (I'll get to that later) but it doesn't matter if this was divine intervention or a misdiagnosis.
While I was pregnant with Beatrix, a number of people came to me with stories about how they knew someone who had received a poor prenatal diagnosis, but who went on to have a perfectly healthy baby.
The implication here was, I should hold on because my physicians may be wrong. My daughter may live -- in fact, maybe all of those things which showed up in the countless tests we had performed were not really there.
The organs growing outside of her body.
Her mangled spine.
Her too large head.
Her twisted feet.
Her paralysis below the waist.
The idea seemed to be that if doctors were wrong she was worth carrying- except even if doctors were right, she was still worth carrying and saving.
We aren't promoting this idea when we say, "maybe they are wrong."
We are expressing we believe a baby misdiagnosed is preferable to one who has been affected. We are separating babies with anomalies from those without.
It doesn't matter.
Or it shouldn't.
But everyone knows it's only common sense for a mother to prefer a healthy baby over one who is ill. That's logical.
But it's not, if you truly believe conception is the beginning of life. If you believe each individual has purpose and fulfills it on a timetable set for them.
If you believe we may not understand everything which will happen in this world, but we know there is One who does- and He understands far more about why my daughter was malformed then I ever will.
It doesn't matter if this child was misdiagnosed or not. If this child would have had all of these issues -- she would still have been the child she was meant to be.
Diagnosis doesn't matter, because she was a human being. The decision to continue a pregnancy should be focused on the fact that a baby in the womb is a human being. Killing human beings is wrong.
Always.
That's what we should focus on. Not the incremental steps. Not trying to convince people through small tugs in the correct direction.
I read this today, "'We know through painful experience that freedom is never voluntarily given by the oppressor; it must be demanded by the oppressed. Frankly, I have yet to engage in a direct-action campaign that was "well timed" in the view of those who have not suffered unduly from the disease of segregation. For years now I have heard the word "Wait!" It rings in the ear of every Negro with piercing familiarity. This "Wait" has almost always meant "Never." We must come to see, with one of our distinguished jurists, that "justice too long delayed is justice denied."'
My daughter was more than a diagnosis, yet every time we toss one of these articles out in the world, we remove the humanity of the small life involved.
As for the accuracy of the original article:
Because one of Beatrix's birth defects was an omphalocele, I am intimately acquainted with the workings of the fetal abdomen.
At 10 weeks- when this woman claims a physician told her that her daughter's organs were positioned outside of her body, and this was a sign of a lethal disorder, it would be completely normal for a baby's intestines to be on the outside of the abdomen. It's part of fetal development. The growth of the intestines outpaces the growth of the abdomen, and for a few weeks early in the baby's life there is a point when they are outside of the abdomen. This lasts until the baby is about 12 weeks GA. A physician would expect to see what would later be called an abdominal wall defect in a 10 week old fetus.
We need to be cautious about sharing emotional stories, without clear details. They do not work well as a testament to our integrity.
The idea seemed to be that if doctors were wrong she was worth carrying- except even if doctors were right, she was still worth carrying and saving.
We aren't promoting this idea when we say, "maybe they are wrong."
We are expressing we believe a baby misdiagnosed is preferable to one who has been affected. We are separating babies with anomalies from those without.
It doesn't matter.
Or it shouldn't.
But everyone knows it's only common sense for a mother to prefer a healthy baby over one who is ill. That's logical.
But it's not, if you truly believe conception is the beginning of life. If you believe each individual has purpose and fulfills it on a timetable set for them.
If you believe we may not understand everything which will happen in this world, but we know there is One who does- and He understands far more about why my daughter was malformed then I ever will.
It doesn't matter if this child was misdiagnosed or not. If this child would have had all of these issues -- she would still have been the child she was meant to be.
Diagnosis doesn't matter, because she was a human being. The decision to continue a pregnancy should be focused on the fact that a baby in the womb is a human being. Killing human beings is wrong.
Always.
That's what we should focus on. Not the incremental steps. Not trying to convince people through small tugs in the correct direction.
I read this today, "'We know through painful experience that freedom is never voluntarily given by the oppressor; it must be demanded by the oppressed. Frankly, I have yet to engage in a direct-action campaign that was "well timed" in the view of those who have not suffered unduly from the disease of segregation. For years now I have heard the word "Wait!" It rings in the ear of every Negro with piercing familiarity. This "Wait" has almost always meant "Never." We must come to see, with one of our distinguished jurists, that "justice too long delayed is justice denied."'
My daughter was more than a diagnosis, yet every time we toss one of these articles out in the world, we remove the humanity of the small life involved.
As for the accuracy of the original article:
Because one of Beatrix's birth defects was an omphalocele, I am intimately acquainted with the workings of the fetal abdomen.
At 10 weeks- when this woman claims a physician told her that her daughter's organs were positioned outside of her body, and this was a sign of a lethal disorder, it would be completely normal for a baby's intestines to be on the outside of the abdomen. It's part of fetal development. The growth of the intestines outpaces the growth of the abdomen, and for a few weeks early in the baby's life there is a point when they are outside of the abdomen. This lasts until the baby is about 12 weeks GA. A physician would expect to see what would later be called an abdominal wall defect in a 10 week old fetus.
We need to be cautious about sharing emotional stories, without clear details. They do not work well as a testament to our integrity.
- Monday, November 10, 2014
- 0 Thank You For Visiting
I stopped. This time not because of an event- but because it was not helpful. I think that for someone exploring their new grief feelings, these types of excersizes can be helpful- but the exploration became negative for me.
There comes a point when we have to walk around the grief that sits too heavily in our hearts. It's like a rabid dog- waiting to bite you. You tiptoe in it's presence, and you let it lie.
This was kicking it awake- and I am not interested in that- being present in my grief. I have been bereaved, but my life is peaceful now. And I have no desire to kick that particular dog.
Some people may see this as burying my head in the sand, but it's not that- it's just reality, and health, and understanding that there is a season for everything under the sun.
I will see her again- so this life shouldn't be filled with her death. That's so wrong- because she was so much more than her death.
She was alive, and that's what I want to capture and hold close. Close my hands around it, keep it sweetly clasped inside of the confines of my heart.
She was alive.
I'm going to share another photo of her, from her life. It will be difficult to see what I want to celebrate, so I am including the original, unaltered photo, and then two more specifying what I am showing you.
An ultrasound at 19 weeks:
- Sunday, November 09, 2014
- 0 Thank You For Visiting
Love makes me light.
And tiny feet.
Listening to music (currently, The Smiths)
Sitting in church.
Gardening.
The light in me comes from the service that I can give to someone else.
In whatever capacity they need.
That room makes me dark. The "what-ifs".
Reading the news and seeing diseased and abused children.
Keeping my service for self-preservation makes me dark.
- Tuesday, October 14, 2014
- 2 Thank You For Visiting
My season would be from the late Fall into early Winter. From the moment of the first falling leaf I begin to walk back into that space where she is still being held so gently in my arms.
The last months of my pregnancy were so terrible. Not because we knew that she was going to die but because we received very little support. The fall was spent traveling to physician's offices, being poked and prodded in an attempt to find out what exactly was wrong.
My family also marks October as a time of loss in general- we don't do well when it comes to October. I lost two cousins on October 25th- 20+ years apart. Brothers- my aunt has been through this baby-loss horror twice, on the same day, decades apart. One baby lost to SIDS and one grown-but-not-grown man to an automobile accident.
My mother will also be gone for two years this October 18th. It seems that the world shouldn't be turning without her in it.
- Monday, October 13, 2014
- 0 Thank You For Visiting
I love music- there is always something playing in the background in my house. I can appreciate a large cross-section of music, but I lean towards either folk music (this comes from growing up with a mother who played classical guitar and who filled my first memories with The Mamas and the Papas, Pete Seger, etc.) or early 90's New Wave music.
In my initial bereavement three CD's were my 24/7 companions.

Dave Matthews Band- Big Whiskey and The GrooGrux King. This CD was the first released after the loss of the DMB's sax player. This measure of pain and remembering was meaningful in helping me to clarify my own thoughts. We used the song "Baby Blue" for Beatrix's memorial video, which is in the left side bar. When you listen to the lyrics it will become immediately apparent why.
Mumford and Sons- Sigh No More. Such a Struggle with God and faith is elucidated in this music. I could identify with some of the frustration about expectations, the anger, and also appreciated the conclusion- the clarification of the Promise.
There is much debate, online, over whether this is a religious album. I think debate is ridiculous- it paraphrases Revelations, the Psalms, directly references heaven and God- while it may not be a "Christian" album, it nevertheless speaks about the relationship between God and Man. I found a lot of comfort in this, and look forward to seeing my daughter with Grace in her heart and flowers in her hair, at the conclusion of this life.
I was given this CD- a friend didn't like it. I didn't think I would either. What a shock to find that it was one of the most meaningful in such an important period in my life. Because it is so obviously about loss, I tried to find information about it online- I was curious to see who he had lost. I found some information leading me to believe that this was based on loss as the result of infidelity. There are some beautiful songs here, and I am so grateful for the happy mistake that brought it my way- the crisp sound of it was a refreshing change from the murky emotions I was feeling.
In my initial bereavement three CD's were my 24/7 companions.

Dave Matthews Band- Big Whiskey and The GrooGrux King. This CD was the first released after the loss of the DMB's sax player. This measure of pain and remembering was meaningful in helping me to clarify my own thoughts. We used the song "Baby Blue" for Beatrix's memorial video, which is in the left side bar. When you listen to the lyrics it will become immediately apparent why.
Mumford and Sons- Sigh No More. Such a Struggle with God and faith is elucidated in this music. I could identify with some of the frustration about expectations, the anger, and also appreciated the conclusion- the clarification of the Promise.
There is much debate, online, over whether this is a religious album. I think debate is ridiculous- it paraphrases Revelations, the Psalms, directly references heaven and God- while it may not be a "Christian" album, it nevertheless speaks about the relationship between God and Man. I found a lot of comfort in this, and look forward to seeing my daughter with Grace in her heart and flowers in her hair, at the conclusion of this life.
I was given this CD- a friend didn't like it. I didn't think I would either. What a shock to find that it was one of the most meaningful in such an important period in my life. Because it is so obviously about loss, I tried to find information about it online- I was curious to see who he had lost. I found some information leading me to believe that this was based on loss as the result of infidelity. There are some beautiful songs here, and I am so grateful for the happy mistake that brought it my way- the crisp sound of it was a refreshing change from the murky emotions I was feeling.
- Sunday, October 12, 2014
- 0 Thank You For Visiting
So.
I have been writing this one since the first day of the photo challenge because when I saw it on the list I understood that it was so important that it would require more attention than the rest of the challenges.
I have to be clear- this is not directed towards anyone- it's solely for me.
A confession of my own convictions.
It's the type of subject that would be a normal post for me as I sort out my feelings about my loss and how it's affected my faith. It's actually something that has been floating around in my head for quite some time now, though slightly different in the specifics.
The definition of altar is as follows:
"an elevated place or structure, as a mound or platform, at which religious rites are performed or on which sacrifices are offered to gods, ancestors, etc."
This is my altar, and it's the only altar that I will ever worship before.
I think that sometimes in this baby loss netherworld- this place where mothers and fathers inhabit the world with one foot in heaven- I must be very cautious in my remembering.
My child is not a god.
And I do not think that she should be worshiped as such-
I am Christian, and I only worship one being.
And that's not my child.
This is the point where I must be clear, and I must separate myself from the mysticism that seems to run rampant throughout the baby loss "community"- and in saying that, I get that some people are are mystics. And I have to say again- this is directed inward, towards me- not them.
I think that it's a beautiful thing to have a special place in my home to keep my Beatrix's memory box, her sweet blankets and the mold of her foot. I see it as no different than the photos I have of my mother, and the quilt that my great-grandmother made.
But an altar?
An altar, by its purest and most correct definition is a place where sacrifices happen.
Where worship takes place.
I think that I must guard my heart, in this instance.
The tendency to fetishize my child is strong.
I would like nothing more than to believe that she speaks to me from beyond the grave, or that I can depend on her for some otherworldly guidance. But the truth is, she doesn't and I can't.
The truth is that she is in Paradise, and I am here, and that my soul longs for what she is already experiencing.
And that she has absolutely no longing for what I am experiencing.
It seems harsh on its face- a brutal statement for the tender heart- but it means so much more.
My daughter would not want me to have an altar dedicated to her- because she is where she is. She is already touching the hand of the Christ who was there at the beginning of the universe- and if she wants anything for me, it is that I join her there. That I don't let anything come between myself and the God who holds her so gently in the palm of His hand.
If she wants anything she wants me to remember with the understanding that she has already received her reward.
That even if my longing for the second chapter of my life to begin is, in part, because I miss her and I want to see her once again- that isn't the focus of my eternity.
This isn't something to think lightly about.
It's an opportunity to reexamine my own convictions and see where I can falter in my own thoughts and actions.
Many may see this as dogmatic, and as a judgement, but I'll be clear again- this is my confession.
My reaction.
The altar in my minds eye is an altar dedicated solely to the Savior who took my sins onto Himself and who redeemed me- and my child- ensuring that while we can not be here together, one day we will be.
- Saturday, October 11, 2014
- 0 Thank You For Visiting
In Memory~
This is my shadow box, with sweet Beatrix's tiny footprint.
We {and our friends/family} have done a number of things in her memory.
My husband and I began a support site for families facing the same diagnosis-
www.limbbodywallcomplex.net
But that will be my inspiration photo, so I'll save more for that later.
One of my close friends is currently training to run a half-marathon in My Bea's memory, for Saint Joesph's Children's Hospital.
Various family members have donated to a number of organizations in her name.
Our current memory project? We are in the process of writing a proposal to our church counsel, to ask that we be allowed to fund-raise for a new playground.
We would like to do this by her 5th birthday, which would be December 2015.
We also have begun planning a new aspect of support which is often overlooked, that we are so excited about- but that's a future goal.
Much of our charitable giving and activities revolve around our daughter- and all of those gifts, whether of time, talent, or money, are done in memory of our daughter.
This is my shadow box, with sweet Beatrix's tiny footprint.
We {and our friends/family} have done a number of things in her memory.
My husband and I began a support site for families facing the same diagnosis-
www.limbbodywallcomplex.net
But that will be my inspiration photo, so I'll save more for that later.
One of my close friends is currently training to run a half-marathon in My Bea's memory, for Saint Joesph's Children's Hospital.
Various family members have donated to a number of organizations in her name.
Our current memory project? We are in the process of writing a proposal to our church counsel, to ask that we be allowed to fund-raise for a new playground.
We would like to do this by her 5th birthday, which would be December 2015.
We also have begun planning a new aspect of support which is often overlooked, that we are so excited about- but that's a future goal.
Much of our charitable giving and activities revolve around our daughter- and all of those gifts, whether of time, talent, or money, are done in memory of our daughter.
- Friday, October 10, 2014
- 0 Thank You For Visiting
Support.
Crutches are the first thing that came to mind when I read the word support. Thinking back to what held me up during my bereavement- which began before Beatrix was even born- I would have to say, yet again, my Bible. I know that most people will write about family members or friends,
and mine were {mostly} great.
But what held me up?
The promise that everything was part of the plan.
That my Bea was part of the creation story- that her very self was integral to the workings of the universe.
What supported me was the promise that while I was on my knees, it would all be for good.
- Thursday, October 09, 2014
- 0 Thank You For Visiting
Resources-
During our pregnancy with Beatrix, we mainly utilized three resources available to women who we're suffering childloss, primarily carrying to term with a poor diagnosis.
Be Not Afraid, an organization which provides information and resources to families facing a difficult pregnancy diagnosis- lethal and non-lethal. We have contributed to their efforts by sharing Beatrix's story in hopes that we can encourage other moms facing a limb body wall complex diagnosis, to continue their pregnancies.
String of Pearls, which helps women facing difficult diagnosis- we were unable to reach them before we had her, but founder Laura Heune sent me the most beautiful bereavement box after Beatrix's birth. I am so grateful.
Sufficient Grace Ministries, which is a resource for families who have suffered losses of any type, although at the time of my pregnancy they focused mainly on carry to term. They have grown to be one of the largest of these types of organizations and have paired up with Stillbirthday to work as bereavement doulas for families suffering loss in their local areas.
This is our Comfort Bear, which we received from Sufficient Grace Ministries, shortly after we came home from the hospital. My sweet boy claimed her out of the box, and named her Bea Bear. In the beginning, hearing her name was so very painful. Now, I am so pleased that her name is commonplace in our home. She is a little beaten up, but to me- she is beautiful.
- Wednesday, October 08, 2014
- 0 Thank You For Visiting
My sacred place would have to be home. Inviolate, it houses everything that I love about this world, and keeps us all in each other's reach.
We feed our children here, and help them to grow into adulthood.
And I can appreciate that now, in a new way.
- Tuesday, October 07, 2014
- 0 Thank You For Visiting
Books.
I am a book reader. Since receiving our diagnosis with Beatrix, I have accumulated quite a library of books associated with loss. The majority of them focus on carrying to term with a poor pregnancy diagnosis.
This is just one portion of my shelf:
I found much comfort also in the Bible- the ultimate source of respite in the time since I lost her. The promise made, that I will see her again- that she is a unique individual, that she is not just some amaphorous energy source that I can feel if I try hard enough- I value that knowledge above all else.
- Monday, October 06, 2014
- 0 Thank You For Visiting
I journal here- and I haven't been journaling often, lately. This project is my segue way back into writing. Not really photo challenge worthy, but it is what it is
- Sunday, October 05, 2014
- 0 Thank You For Visiting
Today's challenge is "now".
This is me now. Mom with kid(s).
Older.
I'd like to think wiser, but probably not so much.
I have a difficult time being separated from my children. I need to be with them all of the time, in order to feel completely at peace.
I am leaner and meaner- I have a hard time letting things go, in situations where I think that someone is wrong. The line between my eyebrows is furrowed deep.
- Saturday, October 04, 2014
- 0 Thank You For Visiting
I'm a little behind the times with my challenges- M was ill, and I ended up using my late night "personal" time for sleeping.
My "before" photo is me during my last successful pregnancy, before losing my Bea.
This is me before:
Before I knew that women who did everything right could still have a baby with birth defects.
Before I knew that women in developed America had babies with birth defects.
Before I knew that birth defects didn't always mean a future of surgeries and hospital stays.
Before I knew that you don't have to be a drug addict or an alcoholic to have a baby with birth defects.
Before I knew that there was such an horrific thing as perinatal hospice.
Before I knew that one in four pregnancies will end in loss.
Before I knew that sometimes euthanasia can be practiced passively.
Before I knew that sometimes parents leave the hospital with empty arms.
Before I knew how to retain a calm exterior when I am quaking inside.
Before I knew that the people most interested in your sad stories are usually the ones who you should stay away from.
Before I lost my very, very best friend (32 years, down the drain).
Before I had ever seen a person die.
Before I understood genetics and the probabilities involved in having good genes, and the miraculous thing that is life- so much could go wrong. Each one if us is a miracle.
Before I was who I am now.
- Friday, October 03, 2014
- 0 Thank You For Visiting
Day 2- Heart
Today's subject is heart. As in- who do you carry in your heart?
My Beatrix is tucked deep within mine. Hidden away inside of the aches and fissures caused by her exit.
This is my photo:
Very simple, and because I do not letter or draw well a very poor showing- except for what it is.
These hearts were all the rage when I was in 6th grade, or so. We girls would turn out dozens of them a week.
We all had our perfect heart stencils. Some of them would be fat, flat hearts. Some tall and thin- but they were all perfect for the girl who was using them.
We would carefully cut out our hearts, and then color the edges with a variety of bright colors. Pressing hard and making certain that the crayon on the edge was thick.
Then we would very carefully set our heart on the surface where we wanted our creation to end up- at the bottom of a love note, on a folder, or on an art project. Holding the heart firmly we would use a pencil eraser to smear the colored wax into the surface of our choosing. Careful not to move the heart, so that the outline was clean and straight.
If done correctly we ended up with this- a heart with a many-colored aura. We thought that this was the height of beauty.
Even while I was doing this, my eleven year old son watched over my shoulder, exclaiming- "that's so cool!!" It must be the age.
When I first read the subject for today this was my immediate thought. I wanted only the most beautiful for my sweet Beatrix. And this was the best that I could offer- it was something that I would have shared with her when she had the coordination to utilize this technique herself.
Sometimes we get caught up thinking of all of the big things that we miss- the wedding, grandchildren, school- but it's the little things that kill. The everyday items, like crayon hearts, that make the loss so much more profound- because it's the mundane that makes up the larger part of our lives.
The subject was inspired by the E.E.Cummings poem, "I Carry Your Heart."
i carry your heart with me (i carry it in
my heart) i am never without it (anywhere
i go you go, my dear; and whatever is done
by only me is your doing, my darling)
i fear
no fate (for you are my fate, my sweet) i want
no world (for beautiful you are my world, my true)
and it's you are whatever a moon has always meant
and whatever a sun will always sing is you
here is the deepest secret nobody knows
(here is the root of the root and the bud of the bud
and the sky of the sky of a tree called life; which grows
higher than soul can hope or mind can hide)
and this is the wonder that's keeping the stars apart
i carry your heart (i carry it in my heart)
- Thursday, October 02, 2014
- 0 Thank You For Visiting
Two years ago I attempted to finish the entire Capture Your Grief photo challenge for pregnancy and infant loss month. My mom passed away and I was unable to finish- my grief was too deep to contemplate finding a way to help walk through it.
So, this year we attempt to do it again.
I am a day late posting, but here is my day one, "Sunrise":
Because I work nights, I am unable to get up early enough to catch a sunrise- we also live in the middle of the woods and can not really see the sunrise (or sunset). By the time it is visible to us it has already reached full light- the tops of the trees illuminated. No matter how many times that I have attempted to catch a sunrise here, I have no success.
This is my post for Sunrise- my subsequent baby- sunrise after a very dark night. She is radiant. Her light creeps into every corner and knocks out all of the shadows.
I will also be posting my photos on Instagram, @shebringsjoy.
So, this year we attempt to do it again.
I am a day late posting, but here is my day one, "Sunrise":
Because I work nights, I am unable to get up early enough to catch a sunrise- we also live in the middle of the woods and can not really see the sunrise (or sunset). By the time it is visible to us it has already reached full light- the tops of the trees illuminated. No matter how many times that I have attempted to catch a sunrise here, I have no success.
This is my post for Sunrise- my subsequent baby- sunrise after a very dark night. She is radiant. Her light creeps into every corner and knocks out all of the shadows.
I will also be posting my photos on Instagram, @shebringsjoy.
- Thursday, October 02, 2014
- 0 Thank You For Visiting
Two weeks ago a co-worker said
to me, as we were finishing up our nightly closing tasks, "I needed
to tell you something. I really respect the decision that you made to follow
your convictions and not have an abortion when your daughter was diagnosed with
her birth defects."
If this would have been the end of the statement then we could have called it a night. I would have gone home with the understanding that my Beatrix had impacted yet another life, and that in the future he may have reacted in a positive way if faced with the same situation.
But this was not the end of the statement.
He continued.
"I don't agree with what you did. I think it was (scientifically) wrong, but I respect you for doing what you thought was right."
It baffles me that after almost four years, I still find it necessary to defend the choice made. A choice that wasn't just a personal preference, which I thought was above reproach in our society of "choice", but which was the right choice.
Keep in mind- I never asked him for his opinion. I didn't request his input on a life situation that occurred during a time that I didn't even know him- nor was I looking for any validation of my decision from him. He popped this statement up in the middle of another conversation. No warning, no prelude.
Because I am accustomed to people sharing their opinion about my (personal) decision, I had a number of ready answers to his "scientific" objections to me allowing my daughter to live.
I will tackle the three responses that I gave to him. They are the three most common reasons why abortion for fetal anomalies should remain available for all women, at any point of gestation.
First, we need to be very clear- terminating a pregnancy does not mitigate grief. In fact, some studies have shown that terminating your pregnancy in this situation may make grief feelings more intense- and surprisingly, we are now seeing that grief intensity may be especially high in earlier term abortions. (1) (2)
(The inception of newer, earlier testing may not be the boon that medical professionals are hoping that it will be. The thought that earlier testing may provide better options for families, in terms of ending a pregnancy "before you get attached," may not bear out to be true.)
Traumatic grief has been shown to accompany every single post abortion experience in some studies, (3) (4) with women requiring intense psychotherapy after said termination. (5) (6) (7)
You are not going to mitigate a woman's grief by encouraging her to go through with a termination. In fact, you may be causing more harm- more often than not maternal bonding has already begun. A life with this baby has been imagined. Names may have already been chosen. Mom may feel movements. (1) (8) (3)
In addition, women are often pressured to terminate these types of pregnancies without being given information about carrying their pregnancies to term. Studies have shown that women who choose to terminate a pregnancy where a fetal anomaly has been shown, will often do so within 72 hours of receiving a diagnosis. (9)
Physicians favor termination over carrying to term for liability reasons- and will often pressure families by stating that "time is running out", coercing them into make a tremendously difficult decision before they have been able to gather and process enough information to make a medically informed choice. (10) (11) (12)
Rarely are families given the option of perinatal hospice or any information about choosing to continue their pregnancy.
Overall, opinions which state that a mother must be able to terminate out of concern for the emotional well-being of the mother is based on our emotional response. Studies show, quite definitively, that terminating a pregnancy for fetal anomalies brings no relief to the mother involved and may possibly bring harm.
The mother of an affected child is losing a baby regardless of whether she interrupts her pregnancy or not. By insinuating that termination is some type of cure you are also defining her child as a sickness. It removes the humanity inherent in her baby- well, it removes the humanity of the baby for everyone except for her. Because for her this will always be her baby.
Medicalizing and throwing the situation into the political pool won't bring her baby back- neither will condemning her.
We can do better than this for women.
Giving women information about continuing a pregnancy after an adverse diagnosis is pro-woman.
Most of our emotion response to exception laws are based on the issue of "force". While most people understand that interrupting a pregnancy under these circumstances is traumatic we assume that continuing a pregnancy under these circumstances must be even more traumatic. Termination is seen as a necessary evil- the lesser of two terrible outcomes.
The idea that "forcing someone to carry to term a pregnancy with a poor diagnosis" is somehow damaging is false-
Receiving a poor diagnosis during pregnancy is damaging.
Period.
With either post-diagnosis decision the risks of PTSD and severe depression are heightened.
Because of the relatively recent advent of perinatal hospice programs, there are fewer studies of what the outcomes of continuing these pregnancies are.
The studies that are coming in, though, are quite telling. They solidify the idea that continuing a pregnancy poses no additional risk for a mother who chooses to do so. In fact- they are routinely showing the opposite. That mothers who continue their pregnancies are faring better, emotionally speaking.
There is no denying that the mother who chooses to continue her pregnancy after receiving a poor diagnosis is at risk for a myriad number of psychological issues. Management of this type of pregnancy requires a completely different and new set of standards. (13)
There is no claim here that any mother who chooses to continue her pregnancy will not suffer grief to the degree that a woman who terminates her pregnancy does. However, carrying to term is indeed making a positive difference in women's lives. Studies show that as perinatal hospice programs grow in number, families who make the choice to continue their pregnancies fare better. (14)
And as programs grow and more parents are educated about the numerous options available to them, early estimates show that 80-87% will make the choice to continue their pregnancy. (15)
Once the perinatal hospice model has been explained, and more often, once a physician has addressed the issues involved with fetal pain parents are left to do what comes naturally to them.
Parent their children.
Create a safe space for them.
Make memories.
(And make no mistake, while pro-choice advocates will claim that families are given all options, the options given are slanted to make termination seem like the only option. I wander through the rooms of post-loss carry to term moms. The pressure to terminate is enormous.)
The after- affects of continuing the pregnancy are beginning to show promise as well- with parents stating clearly that continuing their pregnancy was a positive experience. (16)
In closing, all indications show that in the future we will begin to see more evidence that continuing a pregnancy in which a poor diagnosis has been received is a move in a positive direction for women.
In addition, trends seem to indicate that as more perinatal hospice programs become available, more families will willingly choose to continue their pregnancies.
It is important that those who are interested in the "pro-life" cause continue to grow in their understanding of what "fetal anomaly" exceptions in laws entail, in terms of the mental health of the mother involved, as well as the fetus.
We must begin looking past the emotional responses that we all have to this subject, and see what study after study shows- that termination for medical reasons (TFMR) is not the compassionate choice that we believe it to be.
We must understand that woman-centered care necessarily involves a perinatal hospice dynamic in place of terminations, so that a woman carrying an affected baby can be encouraged to continue her pregnancy to it's fruition.
Perinatal hospice is based on available science-based medicine, not solely an emotional attachment or religious conviction.
As a mother who chose to continue a pregnancy in which a lethal anomaly was diagnosed, and who was pressured to terminate throughout, I can say with conviction that having knowledge of perinatal hospice before the end of my own pregnancy would have resulted in a better outcome, emotionally. As it was, for the majority of my pregnancy I received absolutely no support. I assumed that women always terminated these types of pregnancies.
I believed that I was an anomaly myself.
We can do better than this for women.
(1) Seller M, Barnes C, Ross S, Barby T, Cowmeadow P. Grief and mid-trimester fetal loss. Prenatal Diagnosis 1993;13:341-348, p. 344.
(8) Lorenzen J, Holzgreve W. Helping parents to grieve after second trimester termination of pregnancy for fetopathic reasons. Fetal Diagnosis and Therapy 1995 May-June;10(3):147-56, p. 154.; Kolker, op. cit.; and Seller, op. cit.15. Lorenzen, op. cit.
(9) Donnai P, Charles N, Harris R. Attitudes of patients after “genetic” termination of pregnancy. British Medical Journal 1981;282:621-622, p. 622.
(10) Rayburn WF, Laferla JJ. Mid-gestational abortion for medical or genetic indications. Clinics in Obstetrics and Gynaecology 1986:13-71-82, p. 72; Rothman, op. cit, p. 1194; and Blumberg BD, Golbus MS, Hanson KH. The psychological sequelae of abortion performed for a genetic indication. American Journal of Obstetrics and Gynecology 1975;122:799-808, p. 806.
(11) Drake H, Reid M, Marteau T. Attitudes towards termination for fetal abnormality: comparisons in three European countries. Clinical Genetics 1996 March;49(3):134-40, p. 139.
(12) Feitshans IL. Legislating to preserve women’s autonomy during pregnancy. Medical Law (South Africa) 1995;14(5-6):397-412, p. 397.39. Mander, op. cit.
(13) Continuing with pregnancy after a diagnosis of lethal abnormality: experience of five couples and recommendations for management. Chitty, LS, Barnes CA, Berry C. BMJ. 1996 Aug 24;313(7055):478-80.
(14) The Perinatal Hospice: Ploughing the Field of Natal Sorrow. Byron C. Calhoun M.D., Nathan Hoeldtke M.D. May 2000
(15) M. D’Almeida et al., Perinatal Hospice: Family-Centered Care of the Fetus with a Lethal Condition, J. AMER. PHYSICIANS & SURGEONS 11:52 (2006); B.C. Calhoun & N. Hoeldtke, The Perinatal Hospice: Ploughing the Field of Natal Sorrow (2005).
(16) Sumner 2001
If this would have been the end of the statement then we could have called it a night. I would have gone home with the understanding that my Beatrix had impacted yet another life, and that in the future he may have reacted in a positive way if faced with the same situation.
But this was not the end of the statement.
He continued.
"I don't agree with what you did. I think it was (scientifically) wrong, but I respect you for doing what you thought was right."
It baffles me that after almost four years, I still find it necessary to defend the choice made. A choice that wasn't just a personal preference, which I thought was above reproach in our society of "choice", but which was the right choice.
Keep in mind- I never asked him for his opinion. I didn't request his input on a life situation that occurred during a time that I didn't even know him- nor was I looking for any validation of my decision from him. He popped this statement up in the middle of another conversation. No warning, no prelude.
Because I am accustomed to people sharing their opinion about my (personal) decision, I had a number of ready answers to his "scientific" objections to me allowing my daughter to live.
I will tackle the three responses that I gave to him. They are the three most common reasons why abortion for fetal anomalies should remain available for all women, at any point of gestation.
First, we need to be very clear- terminating a pregnancy does not mitigate grief. In fact, some studies have shown that terminating your pregnancy in this situation may make grief feelings more intense- and surprisingly, we are now seeing that grief intensity may be especially high in earlier term abortions. (1) (2)
(The inception of newer, earlier testing may not be the boon that medical professionals are hoping that it will be. The thought that earlier testing may provide better options for families, in terms of ending a pregnancy "before you get attached," may not bear out to be true.)
Traumatic grief has been shown to accompany every single post abortion experience in some studies, (3) (4) with women requiring intense psychotherapy after said termination. (5) (6) (7)
You are not going to mitigate a woman's grief by encouraging her to go through with a termination. In fact, you may be causing more harm- more often than not maternal bonding has already begun. A life with this baby has been imagined. Names may have already been chosen. Mom may feel movements. (1) (8) (3)
In addition, women are often pressured to terminate these types of pregnancies without being given information about carrying their pregnancies to term. Studies have shown that women who choose to terminate a pregnancy where a fetal anomaly has been shown, will often do so within 72 hours of receiving a diagnosis. (9)
Physicians favor termination over carrying to term for liability reasons- and will often pressure families by stating that "time is running out", coercing them into make a tremendously difficult decision before they have been able to gather and process enough information to make a medically informed choice. (10) (11) (12)
Rarely are families given the option of perinatal hospice or any information about choosing to continue their pregnancy.
Overall, opinions which state that a mother must be able to terminate out of concern for the emotional well-being of the mother is based on our emotional response. Studies show, quite definitively, that terminating a pregnancy for fetal anomalies brings no relief to the mother involved and may possibly bring harm.
The mother of an affected child is losing a baby regardless of whether she interrupts her pregnancy or not. By insinuating that termination is some type of cure you are also defining her child as a sickness. It removes the humanity inherent in her baby- well, it removes the humanity of the baby for everyone except for her. Because for her this will always be her baby.
Medicalizing and throwing the situation into the political pool won't bring her baby back- neither will condemning her.
We can do better than this for women.
Giving women information about continuing a pregnancy after an adverse diagnosis is pro-woman.
Most of our emotion response to exception laws are based on the issue of "force". While most people understand that interrupting a pregnancy under these circumstances is traumatic we assume that continuing a pregnancy under these circumstances must be even more traumatic. Termination is seen as a necessary evil- the lesser of two terrible outcomes.
The idea that "forcing someone to carry to term a pregnancy with a poor diagnosis" is somehow damaging is false-
Receiving a poor diagnosis during pregnancy is damaging.
Period.
With either post-diagnosis decision the risks of PTSD and severe depression are heightened.
Because of the relatively recent advent of perinatal hospice programs, there are fewer studies of what the outcomes of continuing these pregnancies are.
The studies that are coming in, though, are quite telling. They solidify the idea that continuing a pregnancy poses no additional risk for a mother who chooses to do so. In fact- they are routinely showing the opposite. That mothers who continue their pregnancies are faring better, emotionally speaking.
There is no denying that the mother who chooses to continue her pregnancy after receiving a poor diagnosis is at risk for a myriad number of psychological issues. Management of this type of pregnancy requires a completely different and new set of standards. (13)
There is no claim here that any mother who chooses to continue her pregnancy will not suffer grief to the degree that a woman who terminates her pregnancy does. However, carrying to term is indeed making a positive difference in women's lives. Studies show that as perinatal hospice programs grow in number, families who make the choice to continue their pregnancies fare better. (14)
And as programs grow and more parents are educated about the numerous options available to them, early estimates show that 80-87% will make the choice to continue their pregnancy. (15)
Once the perinatal hospice model has been explained, and more often, once a physician has addressed the issues involved with fetal pain parents are left to do what comes naturally to them.
Parent their children.
Create a safe space for them.
Make memories.
(And make no mistake, while pro-choice advocates will claim that families are given all options, the options given are slanted to make termination seem like the only option. I wander through the rooms of post-loss carry to term moms. The pressure to terminate is enormous.)
The after- affects of continuing the pregnancy are beginning to show promise as well- with parents stating clearly that continuing their pregnancy was a positive experience. (16)
In closing, all indications show that in the future we will begin to see more evidence that continuing a pregnancy in which a poor diagnosis has been received is a move in a positive direction for women.
In addition, trends seem to indicate that as more perinatal hospice programs become available, more families will willingly choose to continue their pregnancies.
It is important that those who are interested in the "pro-life" cause continue to grow in their understanding of what "fetal anomaly" exceptions in laws entail, in terms of the mental health of the mother involved, as well as the fetus.
We must begin looking past the emotional responses that we all have to this subject, and see what study after study shows- that termination for medical reasons (TFMR) is not the compassionate choice that we believe it to be.
We must understand that woman-centered care necessarily involves a perinatal hospice dynamic in place of terminations, so that a woman carrying an affected baby can be encouraged to continue her pregnancy to it's fruition.
Perinatal hospice is based on available science-based medicine, not solely an emotional attachment or religious conviction.
As a mother who chose to continue a pregnancy in which a lethal anomaly was diagnosed, and who was pressured to terminate throughout, I can say with conviction that having knowledge of perinatal hospice before the end of my own pregnancy would have resulted in a better outcome, emotionally. As it was, for the majority of my pregnancy I received absolutely no support. I assumed that women always terminated these types of pregnancies.
I believed that I was an anomaly myself.
We can do better than this for women.
(1) Seller M, Barnes C, Ross S, Barby T, Cowmeadow P. Grief and mid-trimester fetal loss. Prenatal Diagnosis 1993;13:341-348, p. 344.
(2) Boss, op. cit.19. Kolker, op.
cit.
(3) White-Van Mourik MCA, Connor JM, Ferguson-Smith MA. The
psychological sequelae of a second trimester termination of pregnancy for fetal
abnormality over a two year period. Birth Defects: Original Articles Series
1992;28:61-74, p. 71; and Zeanah CH., Dailey JV, Rosenblatt MJ, Saller, DN Jr.
Do women grieve after terminating pregnancies cecause of fetal abnormalities? A
controlled investigation. Obstetrics & Gynecology 1993;82:270-275, p. 275.
(4) Kolker,
op. cit.; Rothman, op. cit.; and Black RB. A 1 and 6 month follow-up of
prenatal diagnosis patients who lost pregnancies. Prenatal Diagnosis
1989;9:795-804, p. 801.
(5) Furlong
RM, Black RB. Pregnancy termination for genetic indications: the impact on families.
Social Work in Health Care 1984, Fall;10(1):17-34.
(6) Kolker, op. cit; Iles
S, Gath D. Psychiatric outcome of termination of pregnancy for foetal
abnormality. Psychological Medicine 1993 May;232:407-13, p. 407.17. Blumberg,
op. cit.
(7)
A. Kersting et. al., "Psychological impact on women after second and third
trimester termination of pregnancy due to fetal anomalies versus women after
preterm birth--a 14-month follow-up study,"Archives of Women's Mental
Health" 12:193-201 (2009).
(8) Lorenzen J, Holzgreve W. Helping parents to grieve after second trimester termination of pregnancy for fetopathic reasons. Fetal Diagnosis and Therapy 1995 May-June;10(3):147-56, p. 154.; Kolker, op. cit.; and Seller, op. cit.15. Lorenzen, op. cit.
(9) Donnai P, Charles N, Harris R. Attitudes of patients after “genetic” termination of pregnancy. British Medical Journal 1981;282:621-622, p. 622.
(10) Rayburn WF, Laferla JJ. Mid-gestational abortion for medical or genetic indications. Clinics in Obstetrics and Gynaecology 1986:13-71-82, p. 72; Rothman, op. cit, p. 1194; and Blumberg BD, Golbus MS, Hanson KH. The psychological sequelae of abortion performed for a genetic indication. American Journal of Obstetrics and Gynecology 1975;122:799-808, p. 806.
(11) Drake H, Reid M, Marteau T. Attitudes towards termination for fetal abnormality: comparisons in three European countries. Clinical Genetics 1996 March;49(3):134-40, p. 139.
(12) Feitshans IL. Legislating to preserve women’s autonomy during pregnancy. Medical Law (South Africa) 1995;14(5-6):397-412, p. 397.39. Mander, op. cit.
(13) Continuing with pregnancy after a diagnosis of lethal abnormality: experience of five couples and recommendations for management. Chitty, LS, Barnes CA, Berry C. BMJ. 1996 Aug 24;313(7055):478-80.
(14) The Perinatal Hospice: Ploughing the Field of Natal Sorrow. Byron C. Calhoun M.D., Nathan Hoeldtke M.D. May 2000
(15) M. D’Almeida et al., Perinatal Hospice: Family-Centered Care of the Fetus with a Lethal Condition, J. AMER. PHYSICIANS & SURGEONS 11:52 (2006); B.C. Calhoun & N. Hoeldtke, The Perinatal Hospice: Ploughing the Field of Natal Sorrow (2005).
(16) Sumner 2001
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