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Doha, State of Qatar
Born: August 30, 2004
Died: November 10, 2004
Daddy & Mommy: Glenn & Christel Todd
Ryan, our firstborn, was not an ordinary baby but a special gift from God.
My husband Glenn and I are South Africans, we have been living in the Middle
East for the past 5 years. First Saudi Arabia later moved to Qatar where
Ryan was born. I was 8 months pregnant with Ryan, when Glenn learned that he
had been assigned on a project in the State of Qatar.
We were so excited to move to a new country and the joy of having our first
little baby. Ryan was born on August 30, 2004 at 18:00 with an emergency
caesarian (my water broke) in Doha Clinic, a private clinic in Qatar. After
his birth, I had a feeling ‘something’ was wrong. Within hours of his birth,
deep concerns were voiced due to indications that he had Trisomy 13 – a
chromosomal disorder. Never heard of this syndrome, but within weeks we’ve
became experts on the subject!
After he was born, they transferred Ryan to the Neonatal Intensive Care Unit
in the State Hospital. Glenn went with him and when Glenn came back to see
me at the clinic, I could tell just by looking at him and seeing the sadness
on his face…he told me that the Doctor who admitted Ryan to the NICU said
that he will not make it through the night. But Ryan, the little fighter
that he was, proved the doctors wrong, he wanted to live!
I felt so lonely, being in a foreign country with no friends or family close
by for support. I did not see Ryan until 2 days later. I was scared and did
not really want to look at him. Glenn touched his leg and talked to him.
Later, Glenn picked him up and sang to him, prayed for him. I felt like an
outsider, like it was someone else’s baby. The doctor on-call came in and
talked to us. He encouraged me to hold him, take pictures and make the best
of the time we have with Ryan. (Thank God I did!)
The way I cried… non-stop. I cried for that little body, attached to
machines and feeding tubes. I cried for Glenn, who wanted to be strong, who,
after our daily visits with Ryan at the NICU went home and locked himself in
Ryan’s room, crying, holding his little clothes and praying for him. The
question “Why?” and “Why me?” came up more than once. We visited Ryan every
day for three weeks. Then the doctor said Ryan could go home. The only power
we had was love, cuddling, lots of touching and lots of prayers!
We took Ryan home where he got all the love and attention in the world. In
the mean time, we have met so many wonderful people. Anthea, Cornel and
Nicolene, 3 South African ladies who also live with their families in Qatar
and just know how to give and give and give! Apart from them, there were so
many others who supported us, cried with us, prayed with us and had such a
big impact on our lives.
We had to make the best of the time we had with Ryan, he went shopping with
us, he even came to church a couple of times. He touched so many people’s
lives! God definitely had a purpose with Ryan’s life. And we don’t have any
regrets. After all, we’ve learned a lot from Ryan, we learned the true
meaning of unconditional love.
Ryan was at home for 3 weeks when he developed a high fever and started
having seizures. I took him to the doctor who admitted him to the pediatric
unit. After 2 weeks he was discharged. He spent another two weeks at home
with us and quietly, while I was holding him in my arms went to heaven,
early morning of November 10, 2004.
Time is a great healer, I don’t think any mother ever gets over a child’s
death, but as time goes on, we’ve learned to accept and made peace with
God’s will. It is great to know that Ryan is in heaven.
Christel Todd
(South Africans living in Qatar)
christeltodd@yahoo.com
To all the Trisomy 13 parents:
Heaven’s Special Child
A meeting was held quite far from earth
It's time again for another birth.
Said the angels of the Lord above.
This special child will need much love.
His/her progress may seem very slow.
Accomplishments s/he may not show.
And s/he'll require much extra care.
For all the folks s/he meets down there.
S/he may not laugh or run or play;
His/her thoughts may seem quite far away.
In many ways, s/he won’t adapt.
And he'll be known as 'handicapped"
So let's be careful where s/he's sent.
We want his/her life to be content.
Please, Lord, find the parents who
Will do this special job for you.
They will not realize right away
The leading role they're asked to play.
But with the child from above,
Comes stronger faith and richer love.
And soon they'll know the privilege given.
In caring for this gift from heaven,
Their precious child so meek and mild,
Is "Heaven's very Special Child"
By John & Edna Massimilla/fontfamily>
December 1981
The Optomist- newsletter for PROUD
(of Orange County, CA)
Parents Regional Outreach for
Understanding Down's Inc./fontfamily>
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