In August 2011 when I was 36 weeks pregnant with my second daughter, Chloe, my whole world fell apart. At a routine ultrasound, it was discovered that she had a serious heart defect that would require surgery. This was bad enough but upon further investigation, it turned out that this particular heart defect was common in babies with Down syndrome. This was a huge shock because I had come so far in what I thought was a normal, healthy pregnancy.
To confirm this diagnosis, I had an amniocentesis. Before the procedure, I was given another ultrasound, this time by an Obstetrician who again told me that there was nothing he could see to indicate that my baby had Down syndrome. I was relieved. Two days later however, the results of the amniocentesis came back and confirmed otherwise. Despite my low risk and all the ultrasounds being clear, my baby had Down syndrome.
I felt so many awful feelings at the time of Chloe’s diagnosis. The grief was indescribable and I found myself thinking, “What the hell?” If this had been discovered before 20 weeks, I would have been offered a termination but now that it was too late for that, I was instead handed information on Down syndrome and told that if I had to choose a disability for my child, this would be the one. That my baby would be beautiful and happy and loving and everything would be alright. This was so difficult to make sense of and my head was spinning!
My knowledge of Down syndrome was very limited and what I already knew scared me. I wanted to learn more so I searched the Internet every night and read everything I could find. I looked at photos, read stories and information about the potential health issues and physical characteristics that my baby may have. I was frightened for my family and especially for my 4 year old daughter, Emma. My heart broke when I thought about what this would mean for her. She was so excited to be having a baby sister but now I worried how this would impact her life. Everything was going to be so different. I expected the worst and it hurt. It hurt so bad. This was not what I wanted for myself, my husband and especially not for Emma.
Finally the day of Chloe’s birth arrived. This moment was one that I had been so afraid of. But the whole experience of seeing her for the first time was not scary at all. It was beautiful and unique and amazing. Through all my grief and sadness, I had somehow forgotten one very important thing – Chloe is a baby and she is mine! She looked straight at me with her eyes wide and I found myself smiling. She was beautiful. I said hello and covered her little pink face with kisses. I am your Mummy!
It is routine for expecting mums to undergo a screening test for Down syndrome and other less common chromosomal abnormalities during the first trimester of pregnancy. The problem with this screening test is that it does not provide a definitive answer for Down syndrome. It only provides a risk. I have learned that mothers can be given a risk of 1:14000 and still give birth to a baby with Down syndrome. Likewise, a mother can be given a risk of 1:3 and their baby will be born perfectly healthy. The only test that can provide a 100% accurate result is an amniocentesis. This invasive test, however, has a high risk of miscarriage so it is only offered if a mother’s risk of Down syndrome is higher than 1:300.
I do not blame the Sonographers or my Obstetrician for not picking up Chloe’s Down syndrome. They can only see what is on the screen and I understand now that not all babies with Down syndrome have these soft markers. I just wish this had been made clearer at the time of my screening.
As I write this, I can feel the anti-abortionists ready to pounce but in order to make my point, I will be honest and say that if I had have found out early in my pregnancy that Chloe had Down syndrome, it is highly likely that I would have terminated. This decision would have been made out of fear and ignorance. Throughout the screening process, very little information was provided about Down syndrome and the brief information that I received was rather negative. Down syndrome was portrayed as an unwanted condition. There was certainly no mention of it being beautiful and loving and wonderful. The majority of parents who find out early in pregnancy that their baby has Down syndrome sadly do terminate. Maybe there wouldn’t be so many terminations if people were better educated.
Chloe is 7 months old now and I am thankful that we weren’t given the option to terminate our pregnancy. If we had chosen to, terminating her would have been a real tragedy. Having a baby with Down syndrome is nothing like I thought it would be. Chloe is so beautiful and she surprises us every day. When she was 3 months old, Chloe survived open heart surgery and now that she has recovered, she is growing and achieving her milestones which is so amazing. When I look into her beautiful blue eyes, I know she is meant to be here with me.
It is early days yet and I still have so much to learn and discover. I am certainly still fearful of the future, but this fear has so far been much worse than the reality. There is nothing I can do to take away that extra chromosome from Chloe but what I can do is enjoy today and keep an open mind. There is a whole lot of help, opportunity and acceptance out there in the community for those with Down syndrome so already, Chloe’s future looks brighter than I could have ever hoped for.
On the 21st of March, it is World Down Syndrome Day. Seven months ago, at the height of my grief, I would never have imagined myself saying this but I am really looking forward to celebrating my precious Chloe and giving thanks to all the amazing things she has brought to our lives. She makes me want to be a better person and to live a better life and I am very grateful for that.
Suzanne Loveland is a mum of 2 beautiful daughters and she runs her own marketing business, Creative Elements from home. Suzanne is also an aspiring writer and has recently started a blog which you can read here.









Comments
98 Comments so far
What a great post! Congratulations on your beautiful family Suzanne. I’m pregnant with my second baby and whilst my DS likelihood odds are quite tolerable to me, they are considered borderline by the medical profession and I’ve been offered a range of more definitive diagnostic tests (all which have higher likelihood of miscarriage than my baby has of having this condition).
I feel that today we have a lower tolerance for diversity. Realising that DS can be very severe in some cases, I’m not taking my decision lightly but like you say so eloquently, I feel like this person, whoever she turns out to be, has come to me for a reason. And I will love her and nurture her to the best of my ability.
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Your Chloe is just gorgeous! Congratulations to you all, what a beautiful little family!
Personally I didn’t do the 12 week test for DS. I figured if my babies had have come back with a high risk I would have been too hesitant to go for the amnio let alone anything else. What will be will be…..
I was just chatting about this with a friend yesterday. It really saddens me that it is socially acceptable to terminate a baby based on DS. I have nothing against those that do terminate for this reason I am just thinking about it from the perspective of the family/friends of someone with DS or the person themself. How horrifying to live with a syndrome that is socially acceptable as worthy of basically being bred out of society.
Just a sad observation, I hope I haven’t caused offence.
Much love to all those who have ever been in a situation where this decision has needed to made.
And once again…. Chloe you are a gorgeous little gem! May your life and your family bubble over with joy xox
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Suzanne – I wish the whole world could read this.
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http://www.kellehampton.com is a great website/blog if you haven’t already found it
xx
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Agreed! Great blog!
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Lovely article and I’m glad Chloe’s surgery went well.
Peri natal genetic tests are often misleading. My oldest son was diagnosed with an enlarged heart and poorly formed umbilical cord at the 18 week morphology scan and were immediately offered a termination. There was a high chance of heart failure before he was born. I’m pro-choice but had started to feel my son move a few weeks before the scan so we chose to see how things would pan out. Scans, amno etc, my son was born at term, perfectly healthy. He’s just about to turn 4.
When I was pregnant with my second son, I had more intensive morph scans done, everything was fine till my son was born. Although genetic tests were clear, my son was diagnosed with a rare genetic disorder, based on his appearance alone. We are fortunate he will only need corrective surgery but regardless of that, he’s a gorgeous 17 month old and his unique appearance makes he look even more gorgeous (he smiles with his eyes…).
It’s amazing what you think you would do but until you are faced with an actual situation, you never know.
Thank you for making us all more aware of DS.
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How beautiful your daughters are Suzanne, and what a moving, uplifting post to read. Thank you xx
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Chloe is absolutely gorgeous.
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Hi Suzanne
Thanks for sharing your story, it was beautiful to read and brought a tear (or two) to my eye. Chloe and Emma are absolutely gorgeous girls, how proud you must feel, especially after such a tumultuous time late in your pregnancy with Chloe.
When our second daughter was born, my husband’s work friend had her first baby, a daughter as well. She was born with Down Syndrome and as her mum lovely put in a note to all their family and friends ‘our gorgeous daughter has already proved she is cheeky, by sneaking through all the early pregnancy tests!’
All the best for a happy future for your whole family!
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Awww she’s a cutie pie!
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It always makes me sad when I hear of couples aborting because their unborn child has Down Syndrome. Sure, it’s a different journey than what you were expecting but it’s still very much worth having.
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That is so true. I was offered an amnio when I was pregnant as I was over 35 but didn’t take it up as I knew I wouldn’t abort if the test was positive. I have met some beautiful Down Syndrome children during my life and knew I would have coped with what all that entailed. A lovely story and an adorable little girl!!!
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Well, if anyone has two more beautiful daughters I’d be surprised. They are just gorgeous and I’m so happy you’ve written this lovely piece.
When I found out I was pregnant at 42 I was frantic. One of my children had had a terrible injury and needed months of rehab and at the same time I was packing up a large property and moving. When everything settled down I sat on the lounge and felt a kick. For twenty weeks a little life had been hiding away. I thought I’d put on a kilo or two but hadn’t had time to worry about it. As soon as I felt the baby move I knew I was in all manner of trouble.
By the time I had an amneo the pregnancy had already passed the time for legal termination and I was frantic. The ultrasound showed only one artery in the umbilical cord and there were a couple of other indicators for DS.
I will never forget the terror as I waited for the phone call with the results. All I could think about was having to travel to Queensland where I could terminate the baby. My husband and in-laws wouldn’t believe that I hadn’t known I was pregnant for 20 weeks without realising it. I was exhausted but I had good reason to put it down to stress, I wasn’t the least bit sick and I wasn’t showing. They were filthy with me and thought I was just being selfish to expect my husband to support another baby when the others were nearly grown up.
I was nearly mad with worry and misplaced guilt and I now realise I wasn’t in any sane place to make a decision about termination.
The results came back clear for DS and I cried for days.
The thing is, I have a friend with a DS child whom I love – enormously. I don’t know why I thought I should terminate a DS baby. Now that I look back I know if I had terminated I would never have forgiven myself and I don’t think I would have recovered from it.
I was in a place of such terror that I wasn’t thinking straight. For some reason it has become accepted that Down Syndrome babies should be terminated but that is simply not true. They are beautiful children and a blessing. There are challenges but the rewards are magnificent.
I hope that your story gives hope to other women who are facing this situation and I hope it gives them the strength to brave any pressure to terminate if they don’t want to.
All the best to you and your beautiful family.
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Lord, I’d have been shirty with your in-laws and husband. It does take two to tango! I wonder how your husband didn’t even think that you might have been pregnant, even if it wasn’t a planned pregnancy. I’m glad that everything worked out for you though!
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He left before the baby turned 3, Mary J and is rarely heard from. I can’t say I miss him – or the monster-in-law!
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This was a lovely post Suzanne… I know my mum also had similar fears when she gave birth to my downs’ brother and what it would mean for me as a sibling but he has been the biggest gift our family could be given!
I too have recently started a blog and written a bit about downs’ – http://www.harrietkempton.com
All the very best with where ever this journey may take you x
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Beautifully written. You have articulated both the fears and anxiety of a pregnant mum and the love only a mother can have. Being fully informed with all the facts, and knowing how others may deal with the situation is the best way to make a choice. I agree that the information around in utero diagnosis of Down syndrome is negative – it was 13 years ago when I had an amnnio as I was under the 1:300 risk. Shame it hasn’t changed. Thanks for sharing – lots of love to you and your family
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Lovely article Suzanne. You might want to read Kellie Hampton’s blog Enjoying the Small Things. http://www.kellehampton.com/
Start here with the story of the birth of her daughter Nella: http://www.kellehampton.com/2010/01/nella-cordelia-birth-story.html
It is a blog of love and hope and happiness.
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Was just about to post the exact same link. One of my favourite things on the internet, ever.
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Oh, so beautiful! What a dear little girl you have. Have you read Kelle Hampton’s blog? She gave birth to a baby with Down Syndrome, and she was unaware of this until birth. It is a beautiful story of finding beauty out of the unexpected.
By the way, I happen to be pro-life and I fully ‘get’ why someone would want to terminate a pregnancy with this diagnosis, or another similar one. It would not be something I would ever do – I refuse pre-natal testing – but I do understand. What I love about what you have shared is how what you thought was going to be bad turned out to be so beautiful. We never know the beauty in the unexpected unless we give it a go.I’m so glad you shared your amazing girl with us.
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Oh dear, tears on the bus. Thank goodness for sunglasses! Thank you for sharing x
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What a beautiful story. Your girls are both beautiful. How wonderful to to hear such a life affirming story. It does make me think though of the thousands of beautiful children that are not here today because of misinformation and fear-mongering. All children are a gift, some just come wrapped a little differently.
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This is a beautiful article! Anti-abortionists be damned!
Best of luck to you and your little girls
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