This boy needs N1.2m to
live
By TONY OGAGA ERHARIEFE ogaga@sunnewsonloine.com
Sunday, February 10, 2008
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•Baby
Andrew with his parents
Photo: Sun News Publishing
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When the parents of baby Andrew Duku of Bayelsa State conceived
him, their dream had been for a bouncing baby boy. However,
the reverse turned out to be the case. He was born with a
defective heart, a life threatening condition known as perimembranous
ventricular septal defect that could dispatch him to an early
grave.
Ironically, he shares the same birthday with Jesus Christ.
But, rather than bring joy and happiness like Christ did to
mankind, his life and that of his Andrew needs urgent corrective
surgery to enable him live a normal life. Beyond that, he
is a victim of the much-dreaded Down syndrome (a condition
where an individual has 47 instead of 46 chromosomes). Initially,
the fear was that he would not live long. However, he has
clung to life with the firm resolve of a survivor. But fears
are mounting as time ticks by.
According to his parents, Rev. Anthony and Rosemary Duku,
they would not have come to terms with the condition of their
baby but for the assistance of the Down Syndrome Association
of Nigeria (DSAN).
His Birth
“I was preaching in the church last December, on Christmas
day when word reached me that my wife had been delivered of
a baby,” recalled his father, a pastor. “It was
a thing of joy and a lot of people called him different names
and I said that his name is Andrew
because he is going to be a preacher as that was the covenant
I made with God concerning his life.”
Devastated
However, his dream for his child died a stillbirth when two
months later, the unexpected happened: “We began noticing
abnormal growths. We went to a doctor in Warri, who diagnosed
Down syndrome. That was the first time I heard the name so
I was wondering what Down syndrome was.”
Through a family friend, they got in contact with DSAN after
they saw the association's awareness week celebration on Newsline,
a national network programme on NTA.
Said his father: “We quickly got their details and immediately
contacted the association's president, Mrs. Rose Mordi, who
urged us to come to the Ogunlana Drive office of the association
in Surulere, Lagos.
Some few days later, we came to the centre and were taken
to the Lagos University Teaching Hospital (LUTH) for a check
up on the health condition of the child.
That was how we discovered that he had a defective heart!
It was a big blow to us. I was compelled to question God ‘why
are you making me pass through this.’”
According to Andrews’s mother, Rosemary: “I wept.
My husband asked God if tears and sorrow were the covenant
we had with Him. I was discouraged. We couldn’t pray
or preach.”
It took encouraging words from their bishop to confront the
problem head on. The association was also helpful as they
put them through counseling sessions.
According to the Paediatric Echocardographic report, Baby
Andrew has Perimembranous Ventricular Septal defect, which
results in a complete endocardial cushion effect, requiring
urgent cardiac surgery.
For Mrs. Mordi, DSAN's president: “His condition is
critical. We have to put him on anti-heart failure drugs to
sustain him and stabilize his condition because the cardiologist
said that something needs to be done very quickly. In congenital
heart condition, as the baby gets older, the condition deteriorates
because the heart is overworked. We are running against time.
We need to carry out corrective heart surgery as soon as possible.”
Consequently, to save Baby Andrew, DSAN has launched an appeal
to concerned Nigerians at home and in Diaspora to come to
the aid of the child. She pleaded that nothing is too small
towards saving Andrew. The amount needed for his surgery is
N1.2 million.
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