Chelsea Davies - Author of Come Home Ella

Use the code tinysparksella to ensure $1 from your purchase is donated to Tiny Sparks WA

http://www.empoweringresources.com.au/come-home-ella

A few years ago, I began writing children’s literature. I love the way a difficult topic can be approached so gently, with love and care through picture books. I decided I would like to add to the amazing NICU support network by creating a picture book, not only for siblings of newborns who begin their life in NICU, but also to give extended families and friends basic insight and understanding of what it is like. That is why I wrote Come Home Ella…

But first, here is the story of my own NICU journey…  

It was around 2am on 31st July 2013 when my dreams were interrupted by a nightmare of gushing water and sopping wet sheets. My waters broke… but I’m not due for another 3 months!  I must be dreaming… 

I made the hasty decision to drive myself to hospital, leaving my two blissfully sleeping young boys with their extremely bewildered Dad. The streetlamps blurring past on the deserted avenue gave a surreal sensation of moving through an underground tunnel. Surely this is a dream! 

Utterly confused I parked the car and hobbled to the hospitals front entrance. I pressed the afterhours intercom…once… twice… three times… where is everyone!? I knocked loudly on the locked glass doors… it looks deserted! In-between tears I pressed the after-hours intercom continuously until someone finally answered. Ok, calm down, help is on the way, any minute now I will see the man on the other end who says he will meet me at the entrance.  Any minute now….  I tried the buzzer again, the same man answered sounding as confused as I felt, “I think it’s likely you’re at the old entrance; we have recently moved.’ Seriously… what a nightmare! 

News of the new private hospital opening began seeping back into my frantic mind. Luckily, the new location was in the same complex as the old hospital, just a different building. More long minutes passed before a man came into view pushing an empty wheelchair. Gliding through a maze of glass sliding doors and narrow hallways, I am wheeled into a room in the new hospital and helped onto a bed of crisp linen to await my obstetrician. 

Not long after my obstetrician arrived, I learnt of the gaping hole in my uterus, compliments of a fidgety footling breach foetus, with no means of repair. Sympathetically, I am basically told to hold her in for as long as I can!! Hmmm… bed rest for up to 13 weeks with two children under the age of 6 and moving-house in a just few weeks – this is not adding up at all. Wake me up!! 

Two huge steroid shots to the buttocks later, I am being transferred by ambulance to King Edward Hospital and the watchful eye of a leading obstetrician specialising in difficult births. 

I remember the “hospital” smell on arrival… heightened significantly by outrageous pregnancy hormones. A smell I would soon get used to, as I resigned to the fact this will be home for the next few months while my baby ‘amazingly’ continues to develop in a dry, deflated womb.  But hey, there is a crochet group (something I’ve always wanted to learn) – how bad could it be! 

I never did make it to crochet group. Instead, my days involved reading, bad daytime tv, hovering my pen over the custard or ice-cream boxes on my meals card (before eventually ticking both), visits from family and friends, but mostly worrying about what was to come…

Turns out I needn’t had worried for long. Around 7pm on 1st August, exactly one week after I was admitted to King Edward hospital, our baby girl decided it was time to enter the world, at only 28 weeks gestation. Footling breach position did nothing to slow her down, she was coming… fast! 

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One-hour prior to this I had been complaining of what I thought was severe constipation pain to some rather unfortunate visitors – oblivious to the fact it was the beginning of labour (my previous two births had been unavoidable c-sections).  Eventually, after much complaining and laxatives later, I was examined and told I was not only in labour but almost fully dilated! 

Before I knew it, I was rolling full steam towards the birthing rooms. After the next vicious contraction, I thought it might be a good opportunity to enquire about my spinal block. With two previous failed attempts at natural births, I had never allowed myself to believe the possibility of a natural birth for my 3rd, even before I found out she was footling breach (one of the most difficult and dangerous positions for a natural birth).  “Oh, sweetheart, there’s no time for that,” a kind nurse pitifully informed me, masking her disbelief I would ask such a crazy thing!

My daughter caused two speeding fines that night; one for my obstetrician who had only left my hospital bedside two hours before and confident all was going well (just prior to when the “constipation” pains started); the other for my panic-stricken husband after hollering for the neighbours to please come watch our boys. At least one of the two made it just in time! 

With great skill and expertise the experienced obstetrician safely brought our baby girl, Mahli Ella, into a world she was so impatient to see. 

I was emotionally and physically wrecked, no wonder things get blurry from this point on, but I do remember being pleasantly shocked by the sound of a baby’s cry. I don’t know exactly what I had expected but the crying made it all seem… ok. 

In burst the husband! The next image I remember was our baby girl literally wrapped in plastic. A normal procedure for micro prems yet disturbing all the same and an image that will stay with me always.

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Soon after, my husband and I walked into the Neonatal Intensive Care Unit for the very first time. While it was somewhat strange and daunting, it also felt like a sterilised bubble of protection from the outside world for the tiniest, most precious human being I had ever seen. This artificial womb with its highly capable support system would nurture and help us all through this surreal journey. 

And there she was… tiny, beautiful, simply perfect! This time Mahli was swaddled in blankets and wearing the tinniest little beanie I had ever seen. Hooked up to all sorts of machines, unbelievably fragile but oozing inner strength…she was amazing! Now I really knew it was going to be ok. 

Our journey through NICU was, thankfully, not as precarious as we first may have thought. We encountered the usual three steps forward, two steps back scenario but the amazing NICU nurses did well to ease our minds, assuring us it was all part of the journey. The biggest bump for us was the news of a small heart murmur, leading to the discovery of a minor hole in the heart – that amazingly, with the use of only standard ibuprophen, all but closed over. Unfortunately, only to re-open again a later stage. In the end we were told that a hole of this size will more than likely correct itself and true to that advice, it did. 

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While in NICU Mahli had one major de-sat, which is when the baby turns blue from lack of oxygen and cannot breathe. I was not there at the time it happened, which devastated me, and Mahli’s c-pap (breathing device) time had to be increased. A step which was always disheartening when every tiny decrease in c-pap time was such a huge achievement. It was a waiting game indeed but as always, Mahli eventually climbed her way back with no further de-sats. 

Mahli took to breastfeeding sooner than expected – it was an amazing moment and something I had taken for granted with my previous part baby/part leech full termers. The miniscule amount of milk she consumed, compared to the amount I produced was another matter, although an awesome feeling to know the many excessive litres of natural antibody liquid gold, I was pumping every 3-4 hours, day and night, was nourishment for some other babies in the NICU.  

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A huge struggle for me in this journey was to communicate effectively with my two older children, 2 and 5 years old. I had, up until now, been lucky enough to work part-time hours and always present for them. They were both showing signs of confusion and frustration – ok so we have a baby sister – but where is she? Why can’t we see her? And why is she always taking mummy away? I was living in a vicious circle of guilt and I was my own worst critique. 

At home, I was never really present, always thinking of Mahli laying lonely amongst beeping machines, her needs being tended to by extremely capable people but not her own mother’s hands. Missing out on essential skin to skin contact (aka kangaroo care.) I often watched other mothers in the ward setting themselves up for the day to cuddle, read and spend every possible moment beside their precious newborn babies. Yes, many of these were first time mothers and it was neither fair, or rational to compare myself to them, or anyone else, but I was not always a rational person at the time. 

At the hospital I would think about my boys… I had too much time to think. Their sad little faces… I know they were cared for and was extremely grateful to have hands-on grandparents and friends only too happy to help, but it wasn’t enough to stop my guilt. Amidst the 8 weeks Mahli was in hospital my husband contracted the flu. I can’t even imagine the angst he must have felt not being able to see Mahli at all for a good 3.5 weeks. Our boys also got sick on and off, as kids do in the winter months. To add to this my own mother fractured her ankle only days after Mahli was born and was on crutches for 6 weeks! 

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My 5-year-old was in Pre-primary at the time. I remember driving to hospital one afternoon (I tried to go twice a day, straight after morning school drop off and again late evening) to visit Mahli when a friend called and mentioned our boy’s classroom Open Journey Night. Open Journey Night is where all the work the children have worked hard on for the year is showcased and gushed over by parents or carers being led around by their proud little people. I told my friend I would call her right back, pulled over onto the side of the freeway and really, properly cried. I had completely forgotten! It seems such a little thing now but at the time it was enough to put me over. It was my breaking point that was always going to come and also the moment I realised I had to snap out of robot mode and be present again… be where I am, when I am there. I turned around, picked up my son and went to Open Journey night and didn’t feel guilty for I knew I would do the same for Mahli one day. 

With my husband now back to full health, we began going into hospital as a family, while my husband and I took turns to visit Mahli. The boys were not able to see her but accepted this and were happy to tag along, draw, eat ice cream and play in the hospital gardens. They wanted to see where we went; the place their tiny sister grew stronger every day. It made them happy to know exactly where we were and when we would come back and be as much a part of it as they could. 

Days before Mahli came home we had a combined birthday party for the boys (born 2 years and 364 days apart) with all their friends. The day Mahli finally came home, my 6-year-old said to me she was the best birthday present he got out of anything. Super-duper special! Although I am not sure you would get the same answer if you asked him today, especially if Mahli has been in his room!  

We are now a normal functioning (sometimes functional 😉) family. Mahli turns 7 in August, and the boys 10 and 13 at the end of September. Although we naturally tend not to reflect too much on the past and Mahli’s birth, we will never forget those times and the outstanding, life-saving support we received from the NICU staff at the iconic King Edward Memorial Hospital WA, and the love and support from our family, friends and premature baby foundations. 

Come Home Ella is the book I would love to have read to my boys and Mahli when she was born.  If you wish to purchase a copy for yourself, or someone you know, please click on the link provided to the Empowering Resources website and insert code tinysparksella  to ensure $1 from your purchase is donated to Tiny Sparks WA.  

http://www.empoweringresources.com.au/come-home-ella

FREE Milestone Cards

FREE Milestone Cards Are now available to download and print at home!

Huge thanks to our HBF Run Team for making this possible!  We can’t wait to see the display boards hanging in units and parent lounges of Perth Neonatal Units very soon. This will make it easy for parents to access cards as they need them to celebrate every small achievement of life in NICU.

We just LOVE celebrating right along with our families and welcome you to tag us on your social media if you are sharing images @tinysparkswa #tinysparkswa With 36 different cards available there is one for almost every big achievement!

This is just one of the ways we are supporting Western Australian families living life in the Neonatal Unit.

Hop over to the dedicated Milestone Card page to download your own set today.

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"I thought I was living a nightmare."

Blog post by Mum and Volunteer Sheree.

It was a Sunday afternoon and I was relaxing watching Netflix, as I'd been feeling a bit off with a mild headache.  I was 33 weeks pregnant.  I remember laying there thinking surely I can't get much bigger than I currently am, and just thought I was tired from working and that was the reason for my headache.

I had a rough nights sleep that night and called in sick the next morning as I just didn't feel like I had the energy to go.  I had an appointment with my obstetrician that afternoon, but I still just thought what I was experiencing was normal pregnancy symptoms.  It was at that appointment I was told I was being admitted to hospital for observation as I was showing early signs of pre-eclampsia.  I was scared and severely emotional.

My baby was the result of a hard journey through IVF and the very thought of any threat in my pregnancy resulting in anything other than our dram come true, was too much to bare.  I was a total mess.  My night that night in the hospital was full of hourly checks and observations and by morning I was told by my obstetrician than I wasn't to return to work, as I was still borderline pre-eclampsia, but I was fine to head home on bed rest.

I spent the next 4 days sitting on the couch taking it easy, but on Friday night I began to feel off - a little nauseous and that headache was back. I didn’t know whether to think too much into it or whether to go to the hospital. After an hour wondering I decided to at least call the hospital. After telling them how I was feeling they advised me to come in. So off we went to the hospital and I was hooked up to a machine to see how the baby was going. He was doing well, but I was not. The doctor told my husband and I that my liver and kidneys were showing signs of being in distress and whilst it wasn’t an absolute emergency that night, I was to stay in hospital. I thought I was living a nightmare. I was so scared for my baby and the thought of him being born early was too much for me to cope with. I was an emotional wreck.

The next three days were a routine of hourly checks and lots of blood tests. By Monday morning my obstetrician wasn’t willing to hold off any longer and I was to have a caesarean that morning, as my condition had worsened. Again with the freaking out.

The nurses were so supportive. I was taken down to the Neonatal Unit to see where my baby would go when he was born. It was weirdly comforting and intense all at the same time. The nurses talked me through what some of the machines were and what role they would play for my baby. 

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My son was born 3 hours later at 33 weeks and 4 days. He came out crying and weed everywhere, so I was able to hold him before he was taken away. It was this moment I hadn’t wanted to miss out, of all the moments you get when having a baby. I was so amazingly happy and so in love. 

We spent 3 weeks in NICU before my son was able to come home. The nurses and doctors in our nursery were absolutely amazing. I was allowed to be my sons mother. Even though changing a baby with cords is difficult, it was amazing. The day we were told we could take him home, I panicked. We were in this safe little bubble in the nursery and it just seemed so scary that suddenly I really would be totally in charge. 

My son is now 14 months old. He’s endured two surgeries in his short life, but he is healthy, happy and totally adorable. When we think back to our time in the nursery, we just remember how lucky we were that all our little man had to do was grow a little. For some this isn’t the case. The experience has made us more aware of what others sometimes have to go through, and how lucky we are. Every day with our son is amazing.


We welcome you to share your story with us.  Please e-mail your story along with a few pictures to admin@tinysparkswa.org.au with 'Family Story' in the subject.

Social Impact

Late in 2017 we had the pleasure of working with some fabulous students from Curtin University on their project 'Just Causes'.  They were seeking out organisations who have made significant social impact for all manner of reasons.  We were honoured to be approached and can finally share their work with you.  We think it's awesome, but we might be a bit biased, see for yourself.

World Prematurity Day 2017

World Prematurity Day turned into an entire week of celebration and awareness raising for us!

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A huge thank you to CBHS Health Fund who kicked off our week with morning tea at Bankwest Place.

Hundreds of candle packs were put together for distribution through our hospital network to encourage people to 'light it up purple' at 7pm on World Prematurity Day to create a wave of purple light around the globe.

A snack basket was delivered to Fiona Stanley Hospital for their parent lounge along with their candle packs.

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Co-founder's Amber and Madalyn together with Sacha, Rebecca, Joslyn, Imogen, Xavier and Adison attended the King Edward Memorial Hospital social work morning tea where we met a huge number of recent neonatal unit graduates.

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We were honoured to have the support of Her Excellency the Honourable Kerry Sanderson AC who wore purple and Tweeted to raise awareness of the critical issue of premature birth.

The final event of the week was the much anticipated White Collar Boxing fight night #10 'Fight Like a Premmie' held at Crown Pyramid.  More than 1,000 people came together to cheer on the boxers who gave their all.  So wonderful to see Dad Premo win his closely fought bout!

Some amazing businesses were behind the night and we wish to thank:

Ringside Boxing and Fitness

Travel Key & Festival Travel

Gobsmacked Mouthguards

Panchos Mexican Restaurant

Crown Pyramid

J Group Electrical

Kennards Hire

Killarney Autos

Galaxy Doors & Windows

Olistan Consulting

Dale Signs

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We are delighted to announce that the event raised $3,500 for Tiny Sparks WA and a further $3,500 for Women & Infants Research Foundation.  Here are Donna and Darren from Ringside presenting the cheques to Amber.

All over Perth purple lights were shining brightly all night.  We are very grateful for support from the City of Perth, the Bell Tower and the Metropolitan Redevelopment Authority for turning many of Perth's landmarks purple.

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WA your support was yet again astounding!  Many individuals and businesses held events throughout November as part of 'tiny bites for tiny sparks' raising awareness and much needed funds.  We are grateful for each and everyone of you for your support and look forward to making a bigger impact in 2018.