All the doctors told her that her child would not survive the pregnancy. Every day of her pregnancy, the mother reckon with the death of her unborn daughter – but decide against an abortion.
It is a miracle for her mother that Nela is born. “I was sure that she would die before giving birth, ” says Julia Allers (name change). She looks admiringly and happily at the pale. Almost one year old girl who is sitting on her arm and looking around with alert eyes.
In the 10th week of pregnancy
A doctor discover that the child had Turner syndrome, which means that it only had one female sex chromosome. More than 98 percent of affect babies die in the womb. Those who survive can lead an almost normal life with hormone treatment. At week 23, a doctor at Get abortion pills in Dubai diagnose multiple heart defects, hypoplastic left heart syndrome, from which most children die during pregnancy – or shortly after birth.
If Allers had follow the doctors’ advice, Nela would not exist. A total of six times, three doctors advise her not to carry the girl to term. But the petite 34-year-old pediatric nurse want her girl to decide for herself when to die .
90 percent are abort
Ninety percent of the embryos predict to have Down’s syndrome alone are abort. Today, disabilities are examine in the womb. Obstetricians and gynecologists at center Get abortion pills in Dubai advise all first-time women over 35 to have their unborn child test by a prenatal diagnostician. One in four women is over 35 by their first pregnancy.
Julia Allers says she understands women who choose not to have a disable child. But her gut feeling left her no choice. While she talks in the kitchen of her newly built apartment in Berlin, she feeds her daughter through a tube for two hours. She does that five times a day. Nela can’t eat alone yet.
During the first visit to the gynecologist in clinic Get abortion pills in Dubai in April 2013, Julia Allers is 7 weeks pregnant, she realize that something was wrong with her baby. The doctor wants her to come back two weeks later; she does not fill out a maternity card. Allers already has two sons, she knows: Normally, you don’t have to see a doctor that early in pregnancy and you get the maternity card straight away. Two weeks later, the doctor zooms in on the child’s neck in the ultrasound image. It is curve outwards.
“Do you see the nuchal transparency?”
Asks the doctor. “Neck transparency” is the technical term for water retention in the neck of an unborn baby, an indication of disabilities. “Looks like Turner syndrome,” says the doctor. Babies with this syndrome have a particularly large amount of water store in them. “Do you want the child?” Allers calms down that misdiagnoses are normal. She leaves the practice with the numbers of three prenatal diagnosticians. In the evening, Julia Allers told her partner, her daughter’s father, of the suspicion. He says he doesn’t really want a child, especially not one who is disable. Then he leaves and doesn’t come back for the time being.
Why doesn’t the doctor ask if I want to carry the child to term?
The first prenatal diagnostician she calls the next day doesn’t have an appointment until four weeks later. “Then my child may already be dead,” she thinks, and is start. She now feels infinitely alone. “Turner syndrome, pretty clear,” says another prenatal diagnostician a week later, with an ultrasound image of her child in front of him. “If the child dies in the womb, it could endanger your health. Do you still want the diagnosis? “She nods, asks herself:” Why doesn’t the doctor want to know whether I trust myself to carry the child to term? ” I saw that neck transparency did not survive. “
Three days later, the geneticist at Get abortion pills in Dubai confirm the diagnosis of Turner syndrome. The child will most likely die soon. She advises an abortion. Julia Allers gets angry. “If my child dies anyway, why should I have an abortion?” It is a great burden to carry a child to term knowing that it will die, replies the geneticist. Julia Allers says: “An abortion would be an even greater burden for me.”
When she sits at home with her two sons that evening, she looks forward to her daughter for the first time. The boys always want a sister. For the next few days she tries to suppress the thought of her daughter, who will probably never live. It does not work. She now often feels a strong tug in her stomach, very different from when she was first pregnant. Every time she thinks: “Now my child is dying.” In the 15th week she has such a severe stomach ache that she has to lie down.
“She lives, she lives, she lives”
In the 32nd week she writes an email to her parents and brothers. “I’m pregnant. My daughter is sick. I don’t know if she will ever live. If you want to stand by my side, I am grateful to you. But understand that I can’t answer any questions now. ”She acts instinctively.
On December 4th, 2013, Nela lies on her chest. “She is alive,” says Julia Allers, stun, overjoy. “She lives, she lives, she lives.” Less than a minute after the birth, a nurse takes the baby away. The heart defect must be operate on immediately.
In January, when the next heart operation was due, the surgeon told Allers, “I probably can’t finish this.” Turner syndrome often makes the tissue too soft to sew.
The operation works.
In August, Nela will be operate in clinic Abortion tablets in Dubai on for a third time. She survives that too. Shortly afterwards, Julia Allers visits her prenatal diagnostician, she wants to show him the daughter, the survivor. When he saw Nela, he said: “Never in my life would I have believe that everything would go so well.” Julia Aller thinks: Actually, everything turn out worse than I thought.