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Cara
A Story of Regret
I
went in for a normal prenatal check-up whenever I was 18 weeks pregnant.
They drew blood to perform my "triple screen" test to make sure the baby did
not have any problems. I assumed this would go well being that my first
pregnancy results came back perfect. I have a healthy five year old
daughter.
I called the doctor's office about a week later because of some questions
about back pain, and the nurse was so distraught. They had been trying to
reach me for days and couldn't get a hold of me, and needed me to come in to
the office immediately. My Triple Screen had come back showing strong
evidence of Spinabifida. I went in and got a sonigram and was told nothing
by my OB-GYN. She faxed the pictures and notes to a specialist in a larger
city, and scheduled my first appointment with the them for the following
Monday. Keep in mind, this was a Thursday, so I went home thinking that
since my OB didn't tell me anything was wrong, I figured all must be well!
That Monday, Toby and I drove over to Asheville to see the doctor, our hopes
high. We went in to the room and were greeted by a sonigram
technician who spent about 30 minutes or more taking pictures of each and
every part of the baby. She informed us that we were having a little boy,
and Toby was so excited I thought he would float out of the room! As I was
laying on the exam table, I was looking at the screen, and then Toby, and
the screen, and then Toby just so excited to be having a boy, but as I was
glancing back and forth, I began to see the fear on Toby's face. I looked at
the technician, as he was watching her pretty intensely. As she was doing
the sonigram, she kept making these horrified faces. Her eyes began to tear
up, and she excused herself to go and retrieve the doctor.
Only
minutes later, the specialist came in and informed us that things were "not
good at all". She even began to cry, saying this was one of the worst cases
she had seen in all of her years in the field. She proceeded to show us my
son's different abnormalities on the screen. An extra finger on his left
hand (next to the pinky), a cleft or split lip, only 1/4 to 1/2 of his brain
developed, and a blood valve missing in the umbilical cord. My world crashed
right there. Anger, resentment, regret, fear and hatred to every healthy
human being on this earth developed immediately.
Next, the brought in a Genetic Counselor, who explained that they felt very
strongly that my son had a condition called "Trisomy 13". All of his
characteristics matched up, and they wanted to perform some tests. I allowed
them to do an amniocentesis. They told me that it would be somewhat risky,
but thankfully Tristen lived through it. Then they sent it off for a "Phish
Test" I believe. After the test was done, the Counselor sat down and told us
that there was NO HOPE, that Trisomy 13 was a LETHAL condition. That no
human could live with this disorder! I heard the words lethal and not
medically or scientifically possible a thousand times!
I
noticed over that next week that Tristen didn't kick nearly as much or as
hard. Whether it was the stress I was under or the sonigram that did it, I
don't know for sure. But for some reason I feel like the hour long sonigram
wore him out.
My test results came back after waiting the longest week of my life, and I
was told that Tristen did have Trisomy 13 with a Translocation. I
arranged for labor induction 4 days later, and checked in at 6 PM on a
Thursday. I requested one last sonigram before the induction. They
happily brought the machine in to the room, and I could see that his heart
rate had slightly slowed down, and he wasn't moving nearly as much. I told
them to go ahead. They inserted a Cytotek pill into close to my cervix to
bring on contractions. I was given Morphine for the pain. Tristen Aiden
Brown was born at 2:58 AM, February 2, 2007. He was deceased at birth. I
held him and cried. I begged God to let me take his place. I talked to him
and told him how wonderful he was, how beautiful, and how lucky to have been
able to miss this cruel world and go straight to the arms of the Lord. I
admired his tiny feet and hands, and never wanted to let him go. I cried
when I finally had to hand him over to the nurses. The hardest thing I ever
had to do. What would I give to go back to that day and hold him in my arms
again? There isn't enough money in the world. I would give anything,
absolutely anything, to be able to do it all over again. I was uneducated
about Trisomy 13. I feel as though I was mislead.
Months after his departure from this world, I wandered across this website.
While running a search in Google for more information on Trisomy 13, I saw
it plain as day, and literally went nuts. "Living with Trisomy 13: Children
who are alive and healthy today, living with Trisomy 13." What? What
happened to what my genetic counselor said? "Incompatible with Life",
"Lethal", "Not possible". Let me just say that I have retrieved all of my
medical records and told off who needed to be told. I wish I could go back
to that day on the exam table, where that doctor was telling me it was
hopeless. What I wouldn't give...
Cara Thornton thorntoncm@hotmail.com
Sylva, North Carolina, (Western North Carolina)
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Submitted 10-25-07 |

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| Physician's Home
Not Compatible with
Life, a diary of keeping Daniel
By Kylie Sheffield
Prenatal
Diagnosis Information Package -
Compiled by Kylie Sheffield (mum of Daniel, full
Trisomy 13) in consultation with families on this web site |
| LINKS FOR PROFESSIONALS FROM
MEDICAL AUTHORITIES |
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Lethal Language Lethal Decisions
By Tracy K. Koogler, Benjamin S. Wilfond, and Lainie Friedman Ross
©
The Hastings Center. Reprinted with
permission. This article originally appeared in the Hastings Center Report,
vol. 33, no. 2 (2003),” Editorial email:
editorial@thehastingscenter.org.
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Intensive cardiac management in patients with trisomy 13 or trisomy 18
Am J Med Genet Part A.
*Intensive cardiac management consisting of pharmacological intervention for
ductal patency and cardiac surgery was demonstrated to improve survival in
patients with trisomy 13 or trisomy 18 in this series. Therefore, we suggest
that this approach is a treatment option for cardiac lesions associated with
these trisomies. These data are helpful for clinicians and families to
consider in the optimal treatment of patients with these trisomies.
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Show Me the Money: Financial Considerations in Responding to Parental
Wishes.
Benjamin S. Wilfond, MD,
head of Ethics of Seattle Children's Hospital
Watch the Webcast

View presentation (PDF 425KB)
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Noninitiation or Withdrawal of Intensive Care for High-Risk
Newborns
From the American Academy of Pediatrics Committee on Fetus and Newborn
Organizational Principles to Guide and Define the Child Health Care System
and/or
Improve the Health of All Children
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Amniocentesis: The Struggle to Choose
 By Wendy Hogarth, Mother to Jared diagnosed with trisomy 13 at birth.
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Post-Viability Abortions
 Patricia Lee June, M.D, Pediatrician and PPL board member
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WHAT TESTS SHOULD BE DONE
ONCE MY CHILD IS DIAGNOSED
WITH TRISOMY 13? By Christine Nelson MD, Pediatric Hospitalist
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The parents' journey: continuing a pregnancy after a diagnosis of Patau's
syndrome By Louise Locock,
senior qualitative researcher,
Jane & Jon Crawford,
parents of Benjamin
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Values in End-of-Life Decision-Making: Some Implications for People with
Disability By Jennifer Fitzgerald , Barrister of the Supreme Court of NSW.
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Giving Terminally Ill Babies and Their Families an Alternative to
Abortion
 By Liz Townsend
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PRENATAL
DIAGNOSIS: FEARS & EXPECTATIONS
 by Agneta Sutton, Head of Research The Centre for Bioethics and Public Policy
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Post-viability abortions
 by Pediatrician Patricia Lee June, M.D.
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Clinical Case - Patau Syndrome and Perinatal Decision Making
 Ethics Journal of the American Medical Association May 2005, Volume 7
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Trisomy 13 Facts
&
A Guide for
Professionals
From the Support Organization for Trisomy 18, 13 and Related Disorders
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A
Different Kind of Crisis Pregnancy: When There is “Bad News” About Baby By Monica Rafie
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Understanding Grief: A Component of Neonatal Palliative Care
By
Tricia L. Romesberg, MSN, CNNP
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Disability
Matters - Blog - Institute for the Study of Disabilities & Bioethics Dr.
Mark Mostert, from Johannesburg, South Africa, is co director of Regent
University’s Institute for the Study of Disability and Bioethics.
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| Articles on Eugenics, Ethics,
Selective Abortion, Selective Induction and the killing of Disabled Children |
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Personal Qualms Don't Count: Hospital Forces Nurses To Participate In Genetic
Terminations by MARNIE KO
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ESSAYS BY TRISOMY 13 PARENTS
Free
literature to share with your patients |
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WHEN WHAT SEEMS BROKEN IS
PERFECT
By Barbara Farlow (Annie's Mom)
The decision to accept
disability:
One family’s perspective
By Barbara Farlow BEngSci MBA
A Letter to: Pediatric
Physicians, OB-Gynecologists, Geneticists & Healthcare Providers, from ThereseAnn - A parent of a
Trisomy 13 child
How Our
Babies have changed our Lives by Maria Demers
A Mother's
letter to newly diagnosed Families
(Printable to have on hand in your office to give to patients) by
Julie Sexton
Message to
All Obstetricians & Perinatologists
Message to All Physicians,
Specialists, and Doctors Alike by Mary Mabeus
Letters to Physicians -Trisomy 13 Survival Tactics -Patients
Plan of Care - Faith in Action -Considerations in Making a
Specified Plan of Care by Janina E. Arritola
How can anyone say that
these children do not contribute to society, therefore what is the point?
by Melissa Roy
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| Website & Articles for Surgical Procedures for those opting for medical intervention for specific abnormalities.
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What is an Omphalocele?
The method of delivery will be discussed with you as the
time gets closer. The method of delivery is dependent on the
size of the omphalocele. If the size is quite large and
especially if the liver is involved, the doctor may prefer
to do a cesarean section (c-section) to avoid the risk of
injury to the liver. Otherwise, the preferred method of
delivery is vaginal."
Decompressive cranioplasty may improve the clinical symptoms
of children with mild trigonocephaly and intracranial pressure:
report of 56 patients - June 5 2004
Mild trigonocephaly with clinical symptoms:
analysis of surgical results in 65 patients
- June 5 2004 |
| Termination, Abortion the only choice?
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(A must read for Physician’s who advise
parents after early testing and prenatal diagnosis) These women share the immense pain a termination has left on their lives.
When counseled by Professionals they were offered no hope. They were not given
the option of carrying to term and holding their child, if even briefly. Nor
offered the compassionate support this diagnosis requires. Instead these women
felt they had to make the heart breaking choice to end their child’s life.
- - -
A Story of Regret - "Maybe if the professionals we had
talked to had given us more information we would have made a different choice.
To this day, I still live with the pain of the choices we made. Trisomy needs to
have a bigger voice and all the professionals need to be more open minded and
not so much on terminating"
~Katie -
Full Story
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"It is a choice I cannot live with to this day. I look at these pictures,
read your stories and my heart aches. Since I had a D&E, I never even got to
see or hold my daughter."
~Laurie-Beth
Full Story
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After experiencing the effects of an abortion with a previous pregnancy,
Elizabeth shares her experiences with carrying to term a child with Patau
Syndrome - Trisomy 13.
~Elisabeth Slotkin
Full Story
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This is a portion of a speech given by Eagle Forum Alaska President,
Debbie Joslin on the capitol steps, January 22, 2008
Full Story |
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