Inaugural Quiz Night

We are proud to announce our Inaugural quiz night will be held on the 21st March 2015 at the South Perth Community Hall.

Tickets are $25 per person with all profits going towards Tiny Sparks WA support programmes.

Get together a table of eight (including that friend who knows all that seemingly useless information!) and come along for a night of trivia, games, fun and prizes!

Tickets can be purchased using the 'Add to Cart' on this page or head to the Shop to add other merchandise and/or donations.

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Location - South Perth Community Hall
Cnr South Terrace and Sandgate Street
South Perth

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Affirmation

Affirmation

noun

1  The action or process of affirming something.

2  Emotional support or encouragement.

When things become challenging, whether you are on bed rest or in NICU with your baby, it's important to stay positive.  This is often easier said than done.  We have developed a series of affirmations which you are welcome to download, print and share.  We hope that they help you through your journey, especially when times are tough.  Click on the image below to download all 9 of the affirmations.

Olivia's Story Part III (Remainder of NICU and Homecoming)

Now on CPAP and IV free, Olivia’s journey from weeks four through to her eventual homecoming are a much different story to write than that of her birth and first three weeks in NICU, although still an emotional and difficult one (see Parts I and II here).

Dan (my husband) returned to work after those first three weeks and so we started a new routine for visiting the NICU. Dan would go in either before or after work at least every second day and all day on weekends, I started driving myself in Monday to Friday. We would visit together on the weekends.

Olivia had a new neighbour during week two (we were in a pod of only 2 beds and had been by ourselves for a little while) and in the following weeks I had started talking to the baby’s mother, who would become the best company anyone could ask for in the situation, and it helped immensely when Dan had to return to work. The new baby’s mother had a previous premature baby and was a wealth of knowledge for me on expressing, routine, and what we could eventually expect when we were discharged. I will forever be grateful that our babies ended up as neighbours and that I made this new friend.

Over the next few weeks Olivia’s care and management consisted mostly of winding down her oxygen and CPAP requirements (from higher settings to lower settings) and trying to have her gain a good amount of weight. Calories were added to my expressed breast milk and on day 33 Olivia finally reached the magical 1kg mark! I had called in the early hours of the morning to check whilst awake expressing (as they weigh the babies overnight) and was so delighted to discover she had weighed in at 1000g exactly, they checked it twice! I bought in a home made caramel slice for the staff and bought a little stuffed giraffe from the gift shop for Olivia. I made a ribbon collar for it with a tag saying it was for reaching 1kg, and the giraffe is one of the many special keepsakes Olivia will have for her lifetime.

At four weeks and six weeks Olivia had blood transfusions numbers two and three (of four that she would have in total). A few days after her transfusion at six weeks Olivia’s CPAP could be turned down to its lowest setting and on day 49, at 32 weeks 3 days corrected, Olivia was able to try cycling from CPAP to PBF (oxygen via nasal prongs) for just one hour to start with. It turned out to be a big week for Olivia, on day 52 her feeds were moved from 2 hourly to 3 hourly and we also discovered that she was carrying a strand of e-coli that was mostly antibiotic resistant, picked up from another baby in the nursery. This did not make her sick, but did have the potential to, and contact precautions and restrictions on her movements through the nurseries were enacted. We were not allowed to progress normally through the nursery (to HDU and β€˜Two-west’ etc) due to the contact precautions required.

Day 55 saw Olivia transferred from her humidicrib to an open cot for the first time and day 56 saw Olivia have her two-month vaccinations whilst still in NICU! I came in to the nursery at 4:30am to make sure I was there to hold her hand whilst she had the injections, I felt it was one thing that the NICU experience was not going to take away from me as a new mum, my rite of passage in holding my two month old baby whilst they got their first needles.

That weekend we received a phone call to say that Olivia would be in nursery two when we came in to see her next, they had to conduct a rearrangement of the babies carrying the e-coli bug and had set up a new quarantine area in nursery two. We were very excited at first as it felt like a β€˜graduation’ of sorts, however my excitement soon turned to a couple of emotion filled days as the change impacted me more than I realized it would, or that anyone warned that it might. After 58 days of becoming used to one spot in the nursery and knowing every nook and cranny of that spot, the view out the window and the timing of the doctor’s rounds, this was suddenly rearranged and it hit me quite hard. In hindsight it is easy to describe why it was such a change, but at the time it was much harder to reconcile my emotions about the move and a tough couple of days ensued. Fortunately, Olivia’s neighbour and the baby’s mother moved with us, and her friendly company once again helped me. The feeling was mutual and she told me one day that the company and conversation was so helpful to her; we’re still in contact two and a half years later.

Although the physical move to nursery two came on day 58, Olivia became a nursery two level baby on day 71 (at 35+4 weeks corrected), when she was removed from her CPAP full time (remaining on PBF full time), had her caffeine medication ceased and her cardiac monitoring removed. This milestone also coincided with us being able to give Olivia her first proper bath at 10 weeks old! 

Olivia looking a little unsure about her first bath

One of the most difficult things about the last part of any NICU baby’s journey, as any parent will attest to, is that there is no way of telling how long it will be until the end. Also, the fact they become, act and look healthier and closer to β€˜normal’ newborns means that you can’t help but consider tucking them under your arm and insisting that you can handle things at home! The nursing care becomes less intensive (higher baby to nurse ratio) and the process generally becomes frustrating, a lot more frustrating.

It wasn’t until day 90 that Olivia was finally oxygen free, although we were grateful this was before her due date (at 38+2 weeks corrected), it had been a frustrating journey to that point as there had been a change of consultant in that last fortnight and different parameters had appeared to be set as to what level of de-sat would require her oxygen to be reinstated (I refer to the above paragraph detailing frustration!).

The remaining hurdle Olivia needed to master after her oxygen was removed was suck feeding, and on day 98 after a few days of having three suck feeds spaced by only one tube feed, the decision was made to remove Olivia’s feeding tube and see how she would go on all suck feeds! It was a success (just!) and on day 100 we were told that Olivia had met all the discharge requirements and was ready to go home! It was a Sunday morning and believe me, I was ready for this moment. We had installed the car seat and packed a nappy bag that week, I was ready to break out! The consultant then casually said β€œalthough, Olivia is booked for an eye exam on Monday night, perhaps you should stay until after that.” (Eye exams were required to assess for ROP, a product of prematurity and prolonged oxygen requirement. Olivia had stage 1 ROP which self-resolved).  

It may have seemed fairly insignificant to the consultant to ask us to stay another two days with Olivia, and with a justifiable reason for doing so, but I’m sure every parent of a premature baby knows exactly what I would have been feeling at that moment!! β€œAnother TWO DAYS, are you serious!?” (Yes, again refer to the paragraph on frustration!). We reached a compromise, which was that we would be immediately transferred to a mother-crafting room (where I would be able to stay overnight with Olivia for the first time ever) and stay two nights there until after the eye exam.

It was a surreal experience to be left alone with Olivia after 100 days of never having once been alone with her. There were no monitors, no nurses, no noises, it was just us. Unfortunately Dan couldn’t stay with us overnight, but he did stay until late evening each day and go home just to sleep. On day 101 we celebrated both Olivia’s due date and our wedding anniversary in the mother crafting room, after a night of four hours broken sleep (which I thought was a great effort!). My heart raced every time someone knocked on the door, I was still fearful that someone was going to announce there had been a mistake and we had to return to the nursery! After such a long time it still hadn’t sunk in that we would actually be taking Olivia home. But no one did. That evening Olivia had her final eye exam in hospital and the next morning we were told we could leave!! We tucked Olivia in to her pram and paced around the room whilst we waited for her discharge medications from the hospital pharmacy. Once we had those we wheeled Olivia out of the room and down the corridor… it was the most surreal feeling in the world and I must confess to still welling up with emotion every time I think about it! For me, the homecoming day is the most special day of the whole NICU journey and the joy I feel when I hear of any baby coming home (not just Olivia) is overwhelming!

Olivia weighed 2.6kg and measured 46cm on her due date. 

Dan was fortunate enough to be able to take another three weeks off work when Olivia came home and so we made ourselves comfortable and soaked up the start of our new lives at home for that time. We were both so much in love and no amount of sleep deprivation, vomit or poo explosions were going to stop us from thinking that this was the single best thing ever!

Olivia took a very slow and steady approach to weight gain and was mostly off the bottom of the weight curve for her corrected age, but was otherwise healthy and a generally happy baby. I was extremely strict with the health of visitors to the point where we simply limited the number of visitors quite heavily for the first few months. I wasn’t keen on passing Olivia around for cuddles and trips out to public places were definitely off the table. It was a hard line approach and was isolating at times; it is one primary aspect of the β€˜NICU journey’ that doesn’t actually end when you leave hospital. That, and the volume of specialist appointments that need to be attended!

However I do not regret being so strict as Olivia’s health thrived and she has not had one hospitalisation since her discharge. Two and a half years later, Olivia is still petite but otherwise a picture of health and developing on-track for her corrected age. She has just finished Level 1 β€˜Surf Babies’, loves drawing, playing in sand and Peppa Pig! She is a strong willed and determined girl, no doubt a product of the battle she fought so very early in her life!

Above (L to R): Olivia in her pram on discharge day; Leaving the mother-crafting room; Olivia now.


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Her Battle Begins – Olivia’s Story (The first three weeks of NICU)

Part II of III - Part I "Code Blue - Olivia's Birth Story" can be read here

After she was born, Olivia was taken immediately to NICU and my husband (Dan) was told he could see her about 15 minutes later; it was the first update that he had received on either mine or her conditions since leaving me at the theatre doors. I often consider that to be one of the most traumatic moments of that day for either of us; I had the "benefit” of being asleep and unaware.

During the time I was in theatre when Dan was not sure what the outcome would be he had called both sets of grandparents who had both rushed in to the hospital. As per KEMH visitor policy grandparents were allowed to visit Olivia, one at a time, accompanied by Dan.

Dr Wu (my obstetrician) came to see Dan and my mother is with him at the time; they both finally get to hear that I am OK despite losing quite an amount of blood and are also told that another 10 minutes would have resulted in a very different outcome for both Olivia and me.

In the NICU Olivia had two IV lines placed through her umbilical stump and was hooked up to various monitors (to measure heart rate, oxygen saturation, blood pressure and body temperature). Dan stayed with her until approximately 9:00pm when he was told he could come and see me in recovery as I was waking up. I remember drifting in and out whilst waking and asking the nurses there if Olivia was alive and if she had cried. When Dan came in he showed me some photos and told me that the doctors had told him that she was doing well so far.

It took a little while for my blood pressure to be raised and stabilized, but once it was I was transferred back to the ward. Dan and I sat there in shock for some time before he decided to go home and get some sleep quite late that night.

Late the next morning I had my catheter removed and was able to get up for the first time. I was then able to be taken down in a wheelchair to meet Olivia for the first time (as I was under a GA I didn’t even get a glimpse in theatre). When I saw her I instantly started sobbing and telling her I was sorry, over and over. I don't think any amount of shock could have dulled the emotion of that moment, it was intense; Olivia was unimaginably tiny.

One of Olivia’s doctors came over to see me and explained a few things, including that Olivia had an open PDA channel in her heart (common for premature babies) and that ideally this would be closed before any feeds or progression could commence. I do remember asking what I needed to give consent for and what they would just do out of necessity; I felt as her mum I should have been doing something, even if it was just saying 'yes' to all of the medical team looking after her; I felt quite helpless.

Later that day it was discovered Olivia had a pneumothorax (collapsed lung) and she had an ICC drain inserted in her chest to try and resolve this (to remove the air). She was placed back on a warmer bed which was covered with cling film (literally glad wrap) whilst this resolved because the draining mechanism combined with all of the IVs and monitors she was hooked up to meant that she could not be managed in a humidicrib. She was sedated with morphine and not weighed for a few days due to her fragility. This was another set back both to being able to attempt to progress from mechanical ventilation to CPAP and for feeding, we were told.

Olivia with an ICC drain

Dan helping with the cling film

We were very uncertain about Olivia’s prognosis and celebrated her being 24 hours old, then 50 hours; every small milestone seemed like something to cherish as we weren’t sure how long she would be with us for. Although we weren’t necessarily given a prognosis to that effect, she certainly wasn’t doing as well as she could be.

On day four Olivia’s ICC drain was removed, however this only lasts a few hours before it is needed to be reinserted as the lung has again collapsed. As it is now a Monday (Olivia was born on a Friday evening) the main consultant for the fortnight sees us for the first time and discusses that Olivia may need ventilation for quite some time based on the progress with her lungs. In better news, however, he conducts a head scan that is clear for any large bleeds.

On day five after three days of ibuprofen treatment for her PDA, Olivia has a repeat heart scan that shows the PDA is now closed. She also had her ICC drain removed with success and everyone is feeling a little more positive about the situation. Based on this combination of things Olivia had her first 1mL of EBM at 6pm that evening, and tolerated it well.

I was discharged on day six and cried the entire car trip home. It was agonizing to think that I wouldn’t be under the same roof as Olivia and that I was leaving her behind. I called the NICU three times within the first few hours of being home! Those first few weeks I cried often and at so many triggers… seeing a mother with her healthy full term baby, seeing a heavily pregnant woman, seeing Olivia struggle… everything had me in tears, which those close to me will know is not a common occurrence. The trauma of the NICU experience should never be underestimated, even for the most stoic of mothers.

On day seven Olivia is trialed off the mechanical ventilator and on CPAP for the first time, she only lasted a few hours before needing to be re-intubated. It was not entirely unexpected due to the poor start she had with her lungs.

The following day the last of Olivia’s umbilical lines were removed and a β€˜long line’ was inserted through her foot to replace these. I couldn’t watch it be performed and we had to take a quick break in the parents’ room whilst the consultant performed the delicate procedure. Afterwards Olivia had another spell under the lights for her jaundice levels, another common occurrence for premature babies.

Days nine and ten saw the first and then second day without any procedures performed on Olivia, it was a break for everyone’s stress levels and we embraced the little bit of calmness that came along with it. On day 11 her weight has increased to 726g and her feeds have increased to 3mL every two hours. Although this was all positive I was still not able to hold Olivia and my emotions were getting the better of me as I felt so hopeless; however these few days would prove to be the calm before the storm!

Olivia’s oxygen requirement started increasing and her desats became more frequent; we were told that she needed a blood transfusion (as she was not able to make her own red blood cells yet) and that that may assist in with her oxygenation. Olivia’s feeds were stopped in preparation of the transfusion, however in conducting some other checks before the transfusion commenced it was discovered that she had an infection. Antibiotics were started immediately and the transfusion is delayed a little, but still went ahead.

A lumbar puncture was performed without any anesthetic (the norm, just a little sugar is given before the procedure) and the long line was removed in suspicion that it may have been a source of infection, which turns out to be the case. Olivia’s tiny 700g body was battling a staph infection. We had been told early in our NICU journey that infection was often a matter of β€˜when, not if,’ so whilst somewhat prepared to hear such news, it was still a devastating blow. 

Less than a day after this diagnosis Olivia started having seizures, her oxygen drops dramatically, her colour changes and she makes small repetitive jerking movements. Fear and confusion are added to our devestation and we are once again lost not knowing what to expect.

EEG brain monitoring

On day 15 Olivia was still being treated for infection and still having some seizure activity. She had an EEG performed (a brain scan), and was started on medication whilst a consult was sought from the consultant neurologist at PMH.

My first hold, Day 15

Olivia was still ventilated, but despite all this, I finally was able to hold Olivia for the fist time! It was an emotional turning point for me and I felt empowered and I felt properly like her mother for the first time. I have since given this feedback to Olivia’s neonatologist and commented to anyone who will listen that the first hold is so important for emotional wellbeing.

On day 18 Olivia was finally well enough to have her feeds restarted. The seizure activity was put down to the infection as no other brain abnormality or bleed could be found and they had resolved with the infection. Progress was made in leaps and bounds over the next two days and on day 20 Olivia was finally able to switch from the ventilator to CPAP, and remain on CPAP!

Finally on CPAP and eyes starting to open, Day 21

The following two days Olivia opened her eyes a little for the very first time (they were still fused closed when she was born) and we were also able to hear a tiny little squeak of a cry for the very first time. The last of her IV lines were removed as she was now up to β€œfull feeds” and her oxygen requirement had decreased from 50% down to approximately 35%.

It is only in hindsight that we truly appreciate how sick Olivia was these first three weeks in the NICU and how lucky we are to have such a healthy, thriving two and a half year old today. The team at KEMH are incredible, Olivia is evidence of that fact.

It is the memories of these first few weeks, and my emotional state at the time, which has driven me to want to help other new parents in the same position.

The following 12 (rather less eventful) weeks and Olivia’s eventual homecoming can be read here.


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Giving Tuesday

#GivingTuesday is a movement to celebrate and provide incentives to give. It will culminate with a global day of giving on December 2, 2014

The word cloud below is derived from the emotions parents on our Facebook page shared with regard their feelings going through their high-risk pregnancy or NICU/SCN journey. They are powerful. They are the reason Tiny Sparks WA exists. Families in Western Australia need our support. Please give generously for #GivingTuesday.

How can you get involved in supporting Tiny Sparks WA and #GivingTuesday?

Give Treasure - Donate to our fundraising page here.

Give Time: Fundraise - Set up your own fundraising page here, nominate Tiny Sparks WA as your charity and join the 'Team Tiny Sparks WA', run a morning tea, get your employer to match donations – it’s up to you to show how you support us.

Give Talent - Register as a volunteer and help out throughout the year here.

Spread the Word - By spreading the word about #GivingTuesday you’ll be helping to raise awareness of the ways people can give back, and in turn helping Tiny Sparks WA. Share this #GivingTuesday image on social media and tag @TinySparksWA and 5 friends to encourage them to give something back on 2nd December.

Whatever you give this #GivingTuesday, don't forget to use the hashtag #beCAUSEicare and tag @TinySparksWA @EverydayHero to enter the Everyday Hero competition for your chance to go into the draw to win an iPad Mini.


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