In 2006 my husband Ash and I were amazed and delighted to become pregnant with triplets. However our hopes and dreams for our instant family were dashed when my waters broke, just 21 weeks into the pregnancy.
Five days later, our first son Henry was born, so beautiful and perfect and looking just like Ash. He gave a tiny cry and was laid on my chest where, for one precious hour, I held him and felt his heart beating against mine. His tiny hands squeezed onto our fingers and then, an hour after he was born, he passed away.
Incredibly Henry’s siblings didn’t follow their brother into the world that day. As intervention isn’t given to babies born before 24 weeks, we had a long way to go. But as the days passed our hopes grew.
At 24 ½ weeks, after three weeks of bedrest in hospital, my waters broke once again and Jasper and Evan were born by emergency caesarean. They were immediately intubated and transferred to the neonatal intensive care unit at the Royal Hospital for Women.
Weighing less than a kilo each my boys had a long fight ahead. However, babies this small had survived before and we were optimistic.
The first few days were promising. Both boys were taking my expressed breastmilk through tubes into their stomachs. We spent every day sitting by their humidicribs marvelling at how beautiful they were and falling in love with them.
But when our babies were ten days old we rushed to the hospital in the middle of the night as Evan had taken ill. We sat with him through the night and in the morning learned that he had suffered a severe brain haemorrhage. Heartbroken, we had no choice but to remove him from his life support.
This was the first time Ash and I had held Evan. We told him how much we loved him, kissed him and he slipped away while he was in my arms.
Over the next few weeks Jasper began to grow stronger. Amidst the worry and sadness of this time, we also have some beautiful and happy memories of our time with him. There was the amazing day that he opened his eyes for the first time, the handful of times we were allowed to take him out of his crib for a cuddle, and the time I gave him one precious breastfeed.But, like many such premature babies, our baby had chronic lung disease. Jasper’s lungs kept collapsing and many times over the next few weeks we came close to losing him. However each time he amazed his doctors and fought on.
At 58 days old Jasper’s lungs collapsed again, but this time he could not be revived. Once again we took our baby out of his crib, and held him while he passed away.
The days and weeks following Jasper’s death were terribly hard. Ash and I talked about them all the time, and about the incredible love that they had brought into our lives. We were determined that they would never be forgotten and that something good would come from their lives.
When I should have been run off my feet looking after three tiny babies, I instead was facing maternity leave with empty arms. To help me get through the days, Ash suggested I train for a half marathon, and dedicate it to Henry, Jasper and Evan, raising some money for the Royal Hospital for Women in their memory. I asked a few friends to join me and put out a flyer at a few local cafes. That’s where things snowballed and Henry, Jasper and Evan’s legacy was born.
Nine months to the day since Evan and Jasper were born, and six months after Jasper died, I ran the SMH Half Marathon with a team of 98 people! Together we raised $80,000 for new humidicribs. With the help of the Royal Hospital for Women Foundation we set up the Henry, Jasper & Evan Smith Trust Fund, to provide life-saving equipment for critically ill premature babies in the Newborn Intensive Care Unit at the Royal Hospital for Women.
Each year since then I have organised a team to train and run the SMH Half Marathon to raise funds for my boys’ Trust Fund. In the 5 years since they left us, over 700 people have run with me and over $520,000 has been raised in their memory. This has bought ten humidicribs and ten neo-natal monitors, which are saving the lives of hundreds of premature babies just like mine.
Each year a group of amazing people join my team – some are also parents of precious babies who have died, others are parents of miracle children who have overcome their premature start to life. Many are just inspired by my brave little boys! So many generous people support us – Five months of free weekly training is provided for the team by a professional excercise physiologist and runners also get a free team singlet and cap, donated by Running Bare. This year Tommee Tippee have joined Running Bare as our major sponsors. We have loads of fun along the way, and I organise regular social events in the lead up to the race as well as a team after-party.
My goal for 2012 is for a team of over 250 runners – our biggest yet – and to raise $140,000 for two special ventilators which are gentle on even the tiniest lungs, and are urgently needed by the hospital. Please, if you’ve ever thought of running a half marathon, make 2012 the year you do it, and join me in saving premature babies in memory of Henry, Jasper and Evan.
Knowing that my beloved babies Henry, Jasper & Evan are helping other premature babies to live makes me the proudest mum in the world.
Sophie Smith is a primary school teacher and mother of 5 boys – triplets Henry, Jasper & Evan (who died in 2006 following brave fights for life at one hour, nine weeks, and ten days old respectively); Owen (3 and a half) and Harvey (12 months). She is dedicated to raising funds for life-saving equipment for premature babies in memory of her triplets, by organising teams to run the SMH Half Marathon each May.










Comments
66 Comments so far
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Sophie you are such a strong woman, I had twins at 24 weeks and 19 years later , the months they spent in nicu still haunts me, you are an inspiration for all you do .
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Ah, I thought I would come back and revisit the story that has inspired me to be at the taper end of training for the half marathon with Running for Premature Babies. Sophie is an inspiring woman. Out of such a devastating journey comes the strength to not only go on, but to organise a team to raise much needed funds in memory of her triplets. I really can’t believe I’m doing this run, with 350 other team members this year.
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Sophie,
You are amazing. Such an inspiration.
I had a 27wkr in January. She is now home & doing well.
Those NICU days haunt me & will for a long time.
I was also looking for outlet, something to keep me going & thought about running/training. Unfortunately, the 1/2 marathon is too soon as I am breastfeeding & still too raw after everything but I am definitely going to join your running group next year.
I have just ordered a mass of fabric to start sewing premmie gowns. I will then distribute them to NICU’s and SCN in Sydney. Can’t wait to see all the little miracle babies dressed up in some gorgeous fabric gowns! I know how much it meant when after so many weeks I walked in one morning & finally saw clothes on my little girl.
I will write about & put some photos of the gowns/progress on my blog: allthingsmumsnbubs.blogspot.com
Good luck with the run! Your children are blessed to have a mummy like you & I am sure your special little babies are aware of everything you are doing to help others!
MJ x
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Sophie, I have only just stumbled across this article and your story and I sit here with tears streaming down my face and a heavy heart. You are one very inspirational woman and those boys chose well when they chose you for their mummy. I am blessed to have a 10 year old daughter and 18month old twins, and although they all had rocky starts are bright happy and healthy kids today. On days like today where my patience is stretched and the challenges are great, I will think of you and your beautiful boys. My love and best wishes go out to you and your husband and I thankyou for sharing your story. There are many very fortunate families out there that have you to thank for “paying it forward”. xxx
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Sophie, I’m flooding with tears as I write this email. I’m in such awe of your bravery and resilience. I was born premature at 30 weeks, and only recently saw a photo of myself in intensive care when I was a few days old. I can only imagine what my parents went through in those first few months when I was born. I will be signing up to take part in the SMH half marathon and run with your team.
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We would be honoured to have you run on our team. I think it is amazing that you were born so prematurely and are now strong enough to be able to run a half marathon and help other babies born too soon. It makes me cry to think how proud your parents must be!
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Wow, what an amazing family you have! We too are parents of premmie children, our first born was 6 weeks early, going strong at 19 years old, and twin boys, I went into labour at 26 weeks, managed to hold off till 28 weeks, both weighed just over a kilo, then the fight for life began. TJ grew stronger each day and didn’t really have too many complications, Liam on the other hand had a severe brain bleed on day 2, his life hung in the balance for another 6 long months in our NICU here in Hobart. The day we could take Liam home my husband and I literally ran out of the hospital for fear of someone saying there had been a mistake and that he’d have to stay longer. The twins are now 8. Will definitely send a donation, so many people are willing to share their stories, what about a book to raise some more funds as well as to offer hope and support! Love to be involved with that.
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Thank you so much Natasha. To donate you can click on the button on my homepage at http://www.runningforprematurebabies.com.
The direct link to the fundraising page has changed to http://www.givenow.com.au/runningforprematurebabies
Thanks for sharing your story too. Your book idea sounds good – I just don’t think I’ve got the energy to take that on right now.
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Read this today and in absolute floods. I had twin girls at 28 weeks in 2007. They are ok now, but was a very tough first few months and couple of years in and out of hospital.
Such a beautiful sad story and I would love to run it this year. Got a couple of back issues, so can’t run for another week or so. Sarah
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Thanks Sarah, We’d love to have you on the team! To register go to my website http://www.runningforprematurebabies.com
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What a heartbreaking and beautiful story, thank you for sharing. All your boys would be so proud
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Sophie I was directed to your blog by a good friend, Danielle (Southern Highlands). I would be honoured to join your team. How do I sign up?
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Hi Alexandra, That’s great news! Just go to my website http://www.runningforprematurebabies.com and click on ‘register now’. Thank you so much!
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Thank you so much for sharing your story with us Sophie. You are an amazing, courageous and inspiring woman. Having just had my third son (I lost my first son when I was 20 weeks pregnant), I found it absolutely heartbreaking to read your story, but am amazed at all you’ve done to help other premature babies.
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What an amazing lady you are. We lost our little boy Noah at 20 weeks, in 2004, he was anencephalic and clearly not destined to be here. We now have two gorgeous little girls 3 & 6. So often Sophie I want to shout to the world that I have a son, and how much I love him. Your continued fund raising, I believe is your way of doing that. My husband recently bought me a Kate Uber necklace with the girls name on one side and Noah’s on the other…..I wear it proudly, to me it’s my way of showing I am a mother of 3.
Best Wishes with all you are doing Sophie.
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Thank you Kelly. Yes you will always be a mother of 3, and your little Noah will always be as precious to you as your two living daughters. x
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Sophie, best of luck! I wish I could run too
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Tears. God bless you and your family, all of them. I have donated.
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Thank you so much Josie for your generosity. I will send you an update after the race in May to let you know how we get on!
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Sophie, your abiltity to turn such a devasting situation into such a positive, has absolutley inspired me! As the mother of 2 premature kids (now healthy 4 and 2 year olds), I have always felt I needed to give something back. The NICU staff were absolute angels and were not only responsible for the nuturing of our babies around the clock, but they were such a support for my husband and I. In recent years I have been running in fun runs, but have wanted to aim for a half marathon, but have lacked the motivation. I have found my motivation and would love to run on behalf of your foundation.
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Krystie, I am delighted that you will join my team! THANK YOU! It is always extra special to have people on the team who have children who have overcome their premature start to life. I look forward to meeting you. Don’t forget to go to the website (www.runningforprematurebabies.com) and click on the ‘REGISTER NOW’ button!
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Sophie this is a heartbreaking story but you sound like the most courageous woman! Your boys are absolutely beautiful. I can’t imagine what it must have been like to lose them like that and only get such a short amount of time with them. I am so sorry that you had to experience a pain like that. I so admire your strength and what you have done for all those other babies using those machines every day. You should be so proud. This is a fantastic cause. x
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Thank you so much Kathy
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Would love to join your team Sophie, I’m amazed by yours and Ashleys strength along of course with your beautiful little fellas. What brave and tough little boys. Thanks for sharing your story
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Thanks Lisa for joining my team, and running in memory of two very special little people. I look forward to meeting you at training.
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what brave little angels. Tears running down my face. Good on you, Sophie xx
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Thanks Melissa. They really were so brave.
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Thank you for sharing Sophie, we lost our little boy Lachlan stillborn at 21weeks 6 and half years ago. I started running 2 years ago to improve my health and fitness and to date have run a few 10km runs. This year I have toyed with the idea of doing a half marathon…..well no longer. I live in melbourne so will unlikely be able to train with you, but will come up to sydney to do the run. Thank you for your inspiring story.
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Mary I am so sorry that you share my pain, having lost your precious little Lachlan. It will be an honour to have you on our team running in memory of your son. Thank you for travelling so far to run with us!
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As the mum of a premmie I watched many during our time at the hospital share your journey we are Melbourne based and had the rwh Melbourne help out little girl charli but is there a way we can make a donation to you
Congratulations in shifting such a life changing journey to have a positive influence on many premmies futures
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In the story there is a link to the foundation.
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Thank you so much Mandy. I am so glad that your little girl Charli was able to overcome her premature start to life. You can make a donation at http://www.givenow.com/rwhmarathon
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Sophie, I feel like hugging you when I think of what heartache you have gone through and the wonderful memory to your triplets that is ongoing with your fundraising. What an uplifting person you are. You see, my daughter had quadruplets prematurely, naturally conceived, but born too early at 26 1/2 weeks. I as the grandmother, saw the emotional roller coaster she went through. Two babies developed cerebral palsy and have died, not straight away, we thought they were over the worst, but the poor little lungs were so weak. It’s a long story. One strong little girl and a boy survived, he has mild cerebral palsy but is ok. My daughter is still a mother of quadruplets, not twins as a lot of people think.
Good luck with your ongoing fundraising. You are amazing.
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Thank you Pamela. How tragic that you lost your two grandchildren after they obviously fought so hard to live. I am so sorry. Of course your daughter is always a mum of quads, not twins. I am a mother of 5 boys, not 2. I always tell people this.
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THANK YOU from the bottom of my heart for all of these beautiful comments. For those of you so generously wanting to donate, the link is now up on my website. (Or you can go directly to http://www.givenow.com.au/rwhmarathon)
Danielle and Amy, I am really excited to see that you would like to run with me this year. Please go to my website to register. Training begins next Sunday 22nd, in Centennial Park, if you’d like to join us. And Katrina I look forward to meeting you in 2013!
Thank you so much for taking the time to read my story and leave a message. x
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Hi Sophie
Its Danielle again…I’ve been teary all afternoon but so inspired to do this!
I’ll send you an email because I live in the Southern Highlands but still want to run in your team.
D x
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It can happen to you! I’m a young, fit, healthy, active and happy person. My first baby was just like this first triplet born at 21 weeks after I got diagnosed with incompetent cervix (cervix shortens with no warning). The shock and horror of losing a child no one can imagine. Coming back from maternity leave having to explain that my baby was dead, seeing happy families with bouncing babies, ignorant pregnant ladies smoking, it all broke my heart over and over again.
Luckily I got a permanent stitch on my cervix now (Trans Abdominal Cerclage – TAC) in order to have a normal pregnancy. My next baby however was also born prematurely, this time due to sudden labor. She arrived at 33 weeks weighing 2.1 grams and spent 1 month in hospital.
More money is needed into research and facilities. Losing a child or having a prem baby is one of the most difficult things a person can experience.
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I am so sorry that you also lost your first child at 21 weeks, and so understand my pain. I hope your little girl is doing well after her premature start to life. You are right that more money is needed for facilities for critically ill and premature babies in intensive care.
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What a proud Mum you must be Sophie. I have just had my second precious boy and my eyes just welled up listening to your story. Sophie – I bet all five of your beautiful boys are equally proud of their tenacious Mum.
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Thank you so much Jo. Congratulations on the safe arrival of your second little boy!
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My daughter was born at the royal hospital for women at 28 weeks, weighing just under 1 kilo in 2005. She is now a strong, happy and healthy 6 year old. Sophie’s story is so inspiring, what strength and resilience and what a beautiful way to pay tribute to your boys. Your story reminds me how how lucky we are to have our beautiful girl.
My goal for this year was to train fur a half marathon…. I’ve now found the cause and inspiration to do it!
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Danielle, I am delighted that you will run with us, to celebrate your big girl! I am so glad my boys have inspired you to run a half marathon!
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Great effort. I live in Melbourne, I’d love to help fundraise too…have you considered entering the Melbourne half marathon? Let me know if you would like assistance to start a group this year.
Melissa
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Thanks Melissa, that is so kind of you to offer. I won’t enter a team in the Melbourne half, purely because it takes all my time to organise the Sydney one! However, how about travelling to Sydney for the weekend to run with us?!?
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Both of my children were born premmie. My daughter was born at 30 weeks weighing in at 1.68kg. My son was born at 32 weeks weighing 2.3kg. They were both in hospital for over a month. I thank god everyday that they have grown into healthy children (now 7 1/2 and 6 years old). I still can’t watch ads for premmies without sobbing my heart out. It breaks my heart that anyone has to go through the pain of losing a child. I’d love to donate as well. Sophie you’re an inspiration to us all. xx
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Thank you Allison for so generously making a donation. Being the mum of two premature babies you will know only too well how frightening the journey in Newborn Intensive Care is.
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Would love to run it!
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Fantastic, thanks Amy! Don’t forget to register!
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What a heartbreaking and inspirational story.
Thank you for sharing, you are amazing for having the strength to turn your loss into such an incredible achievement.
If I lived in Sydney I would try to run with you too!
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Thanks Samantha!
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I just went to their website and tried to donate, and it says that after 15th December, donations will be accepted… do we know when this will actually happen?
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Thank you so much Jacki. I’m so sorry the donations site wasn’t up and running earlier. It’s all sorted now! The link for donations is http://www.givenow.com.au/rwhmarathon
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I am a new-mum-to-be and will be signing up for 2013 because of your story. Thankyou for sharing.
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Fantastic Katrina! See you in 2013!
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This is such an inspiring story, I have actually met Sophie and Ash as we ran the half marathon with their group a few years ago (a subsequent pregnancy and moving away from Sydney put a halt to us running again with them). What I couldn’t get over was that even after all their suffering they have come through with such grace and determination, they are both incredibly amazing strong people. Even though I have suffered a miscarriage, I cannot even imagine what it is like to lose one child after giving birth, let alone 3.
They have done such an awesome job with their fundraising efforts, I wish Sophie and her family all the best in their future
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Thank you so much!
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Sophie you are an inspiration. having my beautiful daughter a 26 weeker that was under a kg born and in hospital for months with chronic lung disease I dont know what Ide have done if she hadnt made it. Im so sad your boys didnt make it but inspired by what you are doing to help other prem babies. I cant run a marathon but ide love to sponsor someone doing it, how do we sponsor someone for it?
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Thank you so much Kim. I’m so glad your daughter was able to overcome her chronic lung disease. To sponsor the half marathon, you can make a donation at http://www.givenow.com.au/rwhmarathon
You can make your donation in thanks for your daughter if you want to. Just include her name under ‘additional information’ and I will include her details on my website under ‘special children’.
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As a mother my heart was breaking for you reading your story. Your boys will never be forgotten and what an inspiration you must be to all those who know you.
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I don’t know whether to clap and applaud Sophie’s strength, resilience and achievements, or to bawl thinking about the heartache her and her husband have endured……!
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My nephew was born almost 6 weeks early due to a liver problem.
I was overseas at the time and felt extremely helpless.
Thankfully after a short stint in NICU and special care he grew up to be a healthy happy boy.
I have endometriosis, I have tried unsuccessfully to have children.
Inspirational stuff, Amazing work you have done for 3 beautiful boys.
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Sophie, you are an inspiration. What a heartbreaking story with such an amazing outcome. Thank you for sharing.
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I havent had a premmie, but I have had a stillborn daughter and nothing comes close to holding your tiny, lifeless baby in your arms. Nothing.
My subsequent baby was transferred to the NICU after birth for breathing problems…my 9lb 38 weeker! There he was, next to these tiny little 24 weekers, 27 weekers…every day for them was miraculous. I was astounded at their size, and developed a whole new respect for parents of premmie babies. I watched them as they arrived each day, as they had been for months, to pump, and feed, and do skin-to-skin, dress and change.
My little one was able to leave the NICU when his breathing stabilised 5 days later. One exhausted looking mum watched us preparing to leave as she cuddled her 30 weeker. “One day, Riley. One day WE’LL get there.” I heard her say.
Sophie Smith is inspirational.
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I am so sorry that you too lost your precious daughter. Your description of life in NICU is very accurate! I used to dream about the day I thought I’d take my little boys home. When I had a full term baby two years later, the most amazing moment of all was the moment we left the hospital with my baby in my arms. I cried all the way home!
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What an absolutely amazing, inspiring and strong women Sophie is. My heart broke for her, her husband and her 5 boys, reading her story xx
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As a new mum this story brings tears to my eyes and breaks my heart. You stregth and bravery amazed me and I can’t applaud you enough for that. You beatiful boys would have been so proud of you.