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From Ireland To America
May 28 1999, as I walk out of Newark airport I catch my breath as this
    hot, humid, muggy air is going to kill me. I’m dressed in jeans, t-shirt and light
    jacket and trust me this clothing was not near warm enough leaving Ireland. There
    are people everywhere, hustling to get to their next destination. Kieran and Anne
    are there to greet us, they left Ireland two years prior and we will be staying with
    them until we get on our feet.
I originally left Ireland for a summer with a few other friends. We were granted J1
    visa’s, typically a government program, or in our case sponsored by a private
    sector in Philadelphia to promote cultural exchange. The visas are temporary, with
    a grace period after they expire. I grew up on a farm in North West Donegal, eight
    sisters and two brothers, so it was not easy leaving my family, we were really
    close and still are. But the adventures that lay ahead seemed much more
    gratifying then staying home, stuck in the same old rut.
Color and race struck me at first; I could not believe that there were so many
    whites, blacks, brown, Asians, all living together in one country. I know this seems
    foolish, but I grew up in a small country and at that time it was predominantly
    white, and catholic which leads me to my next astonishment. Four different
    churches, four different religious denominations on one street, how was that
    possible. We had two religions in the whole country, Catholics and Protestants
    and they couldn’t get along, let alone worship in the same town. It’s sad I know.
This is why today I choose to raise my children in a country that accepts and has a
    tolerance for diversity, especially in race, religion and ethnicity. This is a country
    that has ample opportunities for those who seek it. As much as I miss my family in
    Ireland, I could not live back there; I could not subject my children to the narrow
    mindedness that comes with growing up in a country that has no tolerance for
    those who are different.
Who am I
A wife,
A daughter,
A sister,
A friend,
A neighbor,
But my biggest accomplishment
in this life is that,
I am a mother.
"In family life, love is the oil that eases
friction,
the cement that binds closer together,
and the music that brings harmony."
Eva Burrows
“Before you were conceived i
 wanted you
 Before you were born I loved you
  Before you were here an hour I
 would die for you
  This is the miracle of Mother's
Pregnancy complications!!
Been there, done that, just another blood test. I was four months pregnant and
  opted to have the screening test done that test for chromosomal
  abnormalities. I had it done when I was pregnant with Michael, so no big
  deal, it will all be fine. There’s no family history of down’s syndrome, or any
  other syndrome. My brother was born profoundly deaf but the doctor said
  that might be related to my Mom’s pregnancy more than a genetic issue. I
  was not that concerned.
I will never forget that Wednesday as long as I live. Michael was 10 months old
   and taking a nap. My doctor called and asked if I wanted her to give me the
   results over the phone, and of course I did. She proceeded to tell me that my
   blood tests came back and that they there was a 75% chance that the baby had
   trisomy 18 (Edwards Syndrome). She basically explained that if the baby
   made it through birth that the chances of living a year was slim, and only 8%
   of the world’s population lives past a year old, and 1% have made it to ten. I
   felt like someone had punched me in the stomach and I couldn’t breathe. As
   if I wasn’t already an emotional wreck, this just added fuel to the fire. My
   husband was my rock, but I caught him crying one late night in his office.
   Thank god for Michael our ten month old, he made everyday worth getting
   up.
The next step was to see a maternity specialist, have
 extensive ultra sounds done, and see where to go from
 there. That was a nightmare, I know these doctors see
 this kind of stuff everyday but I felt like I was just
 another statistic, especially when she suggested that
 we abort to allow science to do their testing. She also
 said that they might not do a cesarean section if there
 was a complication with the baby but it was
 fine, because the baby might not survive anyway. I’m
 not a violent person but I had an outer body experience
 where I was standing there beside her and her head
 exploded. The ultra sound didn’t show any real serious
 problems, the left side of the heart was slightly smaller
 than the right, she said that might be a concern but see
 how it progressed throughout the pregnancy, all other
 organs seemed fine. The baby had small feet, and that
 is sometimes an indication of chromosomal
 abnormalities. She then suggested that I have an
 amniocentesis, but I’d read the statistics and there was
 a risk of miscarriage. This was 2003 and I believe that
 the risks are far less today, so I don’t know if I would
 have done it today. It would have made the next five
 months of my pregnancy much easier knowing for sure.
I basically spent the next five months of my pregnancy in
  and out of the hospital. I had to go and spend a couple
  of hours getting stress test done every Friday, and
  every Tuesday was check fluid and an ultrasound.
  Because of the negative blood test result, even though
  everything else looked fine, doctors would never say
  that everything was fine, that the baby was healthy and
  did not have trisomy 18. I understand that they were
  protecting themselves, but they were putting us through
  misery. There was no human compassion, just the fear
  of lawsuit, I guess.
That was the longest five months of my life. We were
  faced with decisions that would have ended the
  pregnancy when everything was fine. I learned after the
  fact that the rate of false positive blood test is fairly
  common. My issue is with the ultra sound techs that
  clearly saw that everything was fine. We had prepared
  ourselves the best we could by reading literature about
  Edwards’s syndrome, but I don’t think that there is a
  way to prepare; I believe that it would be a learning
  experience.
Here we are today Ryan, you turned
 nine years on October 4th. You were
 born a strong healthy 7lb 12 oz, ten
 toes, ten fingers. No trisomies, or any
 other health problems. Yes your feet
 are small, we can laugh about that
 now.
Trisomy 18 Edwards Disease
http://www.trisomy18.org/site/PageServer?pagename=whatisT18_whatis



1   out of every 2500 pregnancies in the
  United States,
 Associated with medical complications
 Potentially life-threatening
 50% of babies who are carried to term
  will be stillborn, with baby boys having
  higher stillbirth rate than baby girls.
 less than 10 percent survive to their
  first birthdays
Testing for Trisomy 18
There are two types of testing: screening and diagnostic.
    Screening tests indicate a risk, or likelihood that
    Trisomy 18 is present. A triple test called AFP is done
    around about the 16th-18th week of pregnancy. It’s a
    maternal blood screening test that looks for three
    specific substances, AFP, HCG, AND Estriol. It’s is
    typically recommended for pregnant women over
    35, but it is a very important test that all pregnant
    women should have.
Diagnostic tests check actual cells and can determine if
    Trisomy 18 is actually present. I had the screening test
    done, diagnostic testing includes an ammnio and so I
    decided against that.
If the test comes back positive an ultrasound is scheduled
    and a specialist looks for markers of trisomy 18.
A mother’s love
Ten little fingers, ten little toes,
Pouty little lips beneath a pudgy little nose,
You’re a perfect little bundle, full of joy,
Yes that’s right, your Mommy’s little boy.
Ten little fingers, ten little toes,
Many sleepless nights, only Mommy
 knows,
You’re growing up so fast, my little bundle
 of joy,
But you’ll still always be Mommy’s little
 boy.
Ten little fingers, ten little toes,
Me, the author!
My name is Elaine O’Connor. I am a
 senior at University of North Carolina
 at Charlotte, and soon to be an
 Elementary school teacher. I have
 been married for almost 12 years, and
 have a 10 year old son, Michael, 9
 year old son Ryan, and my daughter
 Ciara is 7. They are my life, my life
 literally revolves around them, and I
 wouldn’t change it for the world. I
 would give my life for my children. 

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From Ireland to America: A Mother's Journey

  • 1. From Ireland To America May 28 1999, as I walk out of Newark airport I catch my breath as this hot, humid, muggy air is going to kill me. I’m dressed in jeans, t-shirt and light jacket and trust me this clothing was not near warm enough leaving Ireland. There are people everywhere, hustling to get to their next destination. Kieran and Anne are there to greet us, they left Ireland two years prior and we will be staying with them until we get on our feet. I originally left Ireland for a summer with a few other friends. We were granted J1 visa’s, typically a government program, or in our case sponsored by a private sector in Philadelphia to promote cultural exchange. The visas are temporary, with a grace period after they expire. I grew up on a farm in North West Donegal, eight sisters and two brothers, so it was not easy leaving my family, we were really close and still are. But the adventures that lay ahead seemed much more gratifying then staying home, stuck in the same old rut. Color and race struck me at first; I could not believe that there were so many whites, blacks, brown, Asians, all living together in one country. I know this seems foolish, but I grew up in a small country and at that time it was predominantly white, and catholic which leads me to my next astonishment. Four different churches, four different religious denominations on one street, how was that possible. We had two religions in the whole country, Catholics and Protestants and they couldn’t get along, let alone worship in the same town. It’s sad I know. This is why today I choose to raise my children in a country that accepts and has a tolerance for diversity, especially in race, religion and ethnicity. This is a country that has ample opportunities for those who seek it. As much as I miss my family in Ireland, I could not live back there; I could not subject my children to the narrow mindedness that comes with growing up in a country that has no tolerance for those who are different.
  • 2. Who am I A wife, A daughter, A sister, A friend, A neighbor, But my biggest accomplishment in this life is that, I am a mother.
  • 3. "In family life, love is the oil that eases friction, the cement that binds closer together, and the music that brings harmony." Eva Burrows
  • 4. “Before you were conceived i wanted you Before you were born I loved you Before you were here an hour I would die for you This is the miracle of Mother's
  • 5. Pregnancy complications!! Been there, done that, just another blood test. I was four months pregnant and opted to have the screening test done that test for chromosomal abnormalities. I had it done when I was pregnant with Michael, so no big deal, it will all be fine. There’s no family history of down’s syndrome, or any other syndrome. My brother was born profoundly deaf but the doctor said that might be related to my Mom’s pregnancy more than a genetic issue. I was not that concerned. I will never forget that Wednesday as long as I live. Michael was 10 months old and taking a nap. My doctor called and asked if I wanted her to give me the results over the phone, and of course I did. She proceeded to tell me that my blood tests came back and that they there was a 75% chance that the baby had trisomy 18 (Edwards Syndrome). She basically explained that if the baby made it through birth that the chances of living a year was slim, and only 8% of the world’s population lives past a year old, and 1% have made it to ten. I felt like someone had punched me in the stomach and I couldn’t breathe. As if I wasn’t already an emotional wreck, this just added fuel to the fire. My husband was my rock, but I caught him crying one late night in his office. Thank god for Michael our ten month old, he made everyday worth getting up.
  • 6. The next step was to see a maternity specialist, have extensive ultra sounds done, and see where to go from there. That was a nightmare, I know these doctors see this kind of stuff everyday but I felt like I was just another statistic, especially when she suggested that we abort to allow science to do their testing. She also said that they might not do a cesarean section if there was a complication with the baby but it was fine, because the baby might not survive anyway. I’m not a violent person but I had an outer body experience where I was standing there beside her and her head exploded. The ultra sound didn’t show any real serious problems, the left side of the heart was slightly smaller than the right, she said that might be a concern but see how it progressed throughout the pregnancy, all other organs seemed fine. The baby had small feet, and that is sometimes an indication of chromosomal abnormalities. She then suggested that I have an amniocentesis, but I’d read the statistics and there was a risk of miscarriage. This was 2003 and I believe that the risks are far less today, so I don’t know if I would have done it today. It would have made the next five months of my pregnancy much easier knowing for sure.
  • 7. I basically spent the next five months of my pregnancy in and out of the hospital. I had to go and spend a couple of hours getting stress test done every Friday, and every Tuesday was check fluid and an ultrasound. Because of the negative blood test result, even though everything else looked fine, doctors would never say that everything was fine, that the baby was healthy and did not have trisomy 18. I understand that they were protecting themselves, but they were putting us through misery. There was no human compassion, just the fear of lawsuit, I guess. That was the longest five months of my life. We were faced with decisions that would have ended the pregnancy when everything was fine. I learned after the fact that the rate of false positive blood test is fairly common. My issue is with the ultra sound techs that clearly saw that everything was fine. We had prepared ourselves the best we could by reading literature about Edwards’s syndrome, but I don’t think that there is a way to prepare; I believe that it would be a learning experience.
  • 8. Here we are today Ryan, you turned nine years on October 4th. You were born a strong healthy 7lb 12 oz, ten toes, ten fingers. No trisomies, or any other health problems. Yes your feet are small, we can laugh about that now.
  • 9. Trisomy 18 Edwards Disease http://www.trisomy18.org/site/PageServer?pagename=whatisT18_whatis 1 out of every 2500 pregnancies in the United States,  Associated with medical complications  Potentially life-threatening  50% of babies who are carried to term will be stillborn, with baby boys having higher stillbirth rate than baby girls.  less than 10 percent survive to their first birthdays
  • 10. Testing for Trisomy 18 There are two types of testing: screening and diagnostic. Screening tests indicate a risk, or likelihood that Trisomy 18 is present. A triple test called AFP is done around about the 16th-18th week of pregnancy. It’s a maternal blood screening test that looks for three specific substances, AFP, HCG, AND Estriol. It’s is typically recommended for pregnant women over 35, but it is a very important test that all pregnant women should have. Diagnostic tests check actual cells and can determine if Trisomy 18 is actually present. I had the screening test done, diagnostic testing includes an ammnio and so I decided against that. If the test comes back positive an ultrasound is scheduled and a specialist looks for markers of trisomy 18.
  • 11. A mother’s love Ten little fingers, ten little toes, Pouty little lips beneath a pudgy little nose, You’re a perfect little bundle, full of joy, Yes that’s right, your Mommy’s little boy. Ten little fingers, ten little toes, Many sleepless nights, only Mommy knows, You’re growing up so fast, my little bundle of joy, But you’ll still always be Mommy’s little boy. Ten little fingers, ten little toes,
  • 12. Me, the author! My name is Elaine O’Connor. I am a senior at University of North Carolina at Charlotte, and soon to be an Elementary school teacher. I have been married for almost 12 years, and have a 10 year old son, Michael, 9 year old son Ryan, and my daughter Ciara is 7. They are my life, my life literally revolves around them, and I wouldn’t change it for the world. I would give my life for my children. 