Hey. I am still here.

Hi friends,

I feel I owe you an explanation – a month ago I just vanished. I shut down insta and I felt a sense of freedom, kind of.
If you’ve been following me on instagram for a while you will know I often talk about fantasising about just shutting this all down, vanishing from social media – becoming anonymous… I didn’t think I actually ever would or could though, part of me felt obligated to wake up every morning most days of the week and uplift and encourage other women, to share my highs & lows so other women didn’t feel so alone. I lived for it, I loved it. I felt I was helping others & I felt called to support other women by sharing my story.
But on the night I shut it down something changed, something happened which is as much explanation as I will ever give on this topic in respect to every person involved – but it changed me and suddenly I could no longer uplift and inspire other women because I felt broken and hurt. I felt I couldn’t write positively and fake being ok because I wasn’t – I hate the fakeness of social media and my account has always been under constant scrutiny of being “not genuine” because it appears pretty and curated – but if you took the time to read my posts, read the captions of those styled photos you would realise I don’t bullshit and I’m not fake. I am a real person and I have everything from great seasons to devastating seasons in my life – just like you do & I try my hardest to be very raw about my journey, while maintaining some privacy – because in a world where we share everything – we need to keep some things private.
And my healing in the past month has been something I’ve needed to do away from sharing every detail with a few thousand people.
So read into that what you want, assume what you will. But I won’t be commenting further on it to anyone, this is just another journey to navigate through in another season of our life.
Bottom line though is we are all fine and well.
Well, “well” is open to interpretation – my health is doing ok in one sense and then in another sense I’ve just discovered it’s not so awesome – but that’s just the story of my life.

But ModernWifeLife31 is now gone.
If you’ve noticed on some social media I am rolling out a name change, still struggling with facebook but we will get there…
I don’t feel ModernWifeLife31 was right for me anymore, I’ll get more into that another day…
Does this mean I am coming back to writing weekly and posting daily? No.
For now, I will be doing this for me.
I feel my heart isn’t in this 100% at the moment and I don’t want to force content as I feel that isn’t genuine. The influencer game isn’t something I am that proud of lately, I find it so incredibly fake & forced and people who buy & trade followers, likes & comments kind of disgust me…
I maybe back to normal sooner than I think but I am not sure… I  think I still feel a bit burnt out after all the Christmas content too… Who knows, tomorrow I could wake up and be back 110% or it all may take a little more time. (I am tempted to fire up the ol’ IG though, even just to catch up on everyone I’ve missed so much!)
Edit; it’s back but new name – @bindy_g3
I have wrestled this week if I should return or simply just walk away, I have been constantly pestering trusted people in my life (the whole like 3 of them) with questions, thoughts & new blog name ideas – trying to work this out. I am constantly torn between wanting to share my life & my story because at times I feel almost called to, or just fading away and enjoying what it’s like to be anonymous – because to be honest sharing your life isn’t always wonderful & being private is quiet nice…
But for now I’m kind of back… Dipping my toe slowly back into the online pool but with a new guard up.
As you can see there is a lot of reasons behind my ” out of the blue hiatus”…
I just needed to look after me & I am slowly becoming me again.
I admit I have missed instagram but I did not miss the pressure of needing to post daily & create content. But part of my motivation to coming back was to share some easter content because y’all know I love a good holiday to decorate for.
I know though I need to look after my heart & build myself back up before I can help motivate & uplift my readers… So as I come back I maybe a bit quieter than normal, please bear with me on that.

I know many of you will be wondering how LuLu has gone at big school, she went as expected totally fine. She’s strong & confident and there were zero tears from any of us. She makes us proud.

I also want to take a moment to thank so many of you for your very surprising messages, to be honest it was a little overwhelming but a truly lovely surprise. I didn’t think many people would actually notice when I shut down insta, but so many of you did and I’m sorry for the way I left, but thank you for caring, reaching out and being understanding.

I miss you all.

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Tips on how to have a great year & my goals for 2019.

2018 only has hours left and then we are presented with a brand new year. A year to make our own…

These are my tops tips on how to make 2019 a great year! Yes every year will have hardships and challenges, but we can strive to still make it great and just remember hard times build strength and character!

  1. Review 2018… Go back over the last year, work out what worked best for you and what didn’t. What people lifted you up and who was toxic? What habits made you feel better and which made you feel worse? Assess every aspect of your life, note down what worked and didn’t. Be mindful of these entering the new year and try to do more of the good in 2019.
  2. Set your focus. For some people resolutions work best, for others vision boards, prophetic words or phrases. Whatever works best for you, set it.
  3. Improve your health in someway. We should always work towards better health, perhaps this year you can focus on eating better, drinking more water, visiting the doctor for that check up you keep putting off, quitting a bad habit, seeing the dentist – whatever it is – make it a priority – our health is so important.
  4. Be active – this goes along with point 1, but reflect on your past year and work out what activity you enjoyed most and do more of it! It could be walking, hiking, maybe the gym motivates you, family bike rides or yoga – being active is so incredibly important.
  5. Improve where you live – our living environment reflects and effects our mental state. Work out ways to positively impact your environment, perhaps try organising your home more, decluttering, making a cleaning schedule etc.

So how do I plan to make 2019 a great year?
By following this…

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2018 was a huge year for us, it was huge, busy, chaotic, stressful, exciting, worrying, upsetting and fun and I’m tired from it, so tired.
2019, I want to slow us down, I want to rest, I want less chaos.
In this new year I want to be intentional.
Intentional with my faith, marriage, parenting, words, our money, my choices, my health, my thoughts – just overall be more intentional.
I want to slow everything down, 2019 will still be a big year for us with LuLu starting prep but I want to try TRY and have a calm & slow year. So implementing more organisation, planning & simplifying into our lives, avoiding unnecessary stress & drama, saying “no” more and just allowing space for more quiet in my life.
I also want to grow in 2019, I feel I’ve grown tremendously in the last 2 years – every year we evolve but this year I want to channel my growth into certain areas… I want to grow  in my faith, I pray for more patience and wisdom for my mothering, I want to grow ModernWifeLife31, I can’t physically grow any taller – haha – but I do want to continue to grow personally & emotionally. Every year I aim to grow more, learn more and become stronger.
So that’s my focus for 2019.
I know what bought me great stress & heartache in 2018 and I plan to steer clear of it in the new year. I plan to continue working on improving my health with my specialist, I also want to see a doctor about my back as I have scoliosis, I need to book us all in to see a dentist for a check up and I know we need a skin check up too!
Yoga and walking is something I want to do more of. I really enjoy the calmness of yoga and a yoga class is a nice treat for myself, we live in a nice area and I want to take advantage of that and go for more walks and make it a weekly habit.
As for our home, I feel I am going into 2019 with a clean and organised home – I’ve spent the time between boxing day and new years eve cleaning and organising our home, our space has been reset and we are ready to enter 2019. But we will continue to work on landscaping our block and decorating our home. I also want to continue to declutter our home.
But that’s about it, I have my same general list I stick to each year as well which you can read on THIS blog. 

Well friends, in a few short hours 2019 will be here, I hope 2018 is a year you can look back on fondly even if it’s just knowing you’ve left stronger than how you entered it. And I pray 2019 is a beautiful & great year for you.

Happy New Year, Bring on twenty nineteen! (This is the last year in our lifetime that we will have a year ending in teens!)

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Shortbread recipe.

Hi friends,

I hope you are all having a beautiful December.
Today I did a little Christmas baking (Kringle the elf insisted we do it), so shortbread was made!

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This is my shortbread recipe, I posted it over on Bella In Bindyland years & years ago, but I thought it was worth sharing here!

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It’s a simple recipe but always seems to be a winner. I personally don’t eat a lot of shortbread, so it’s not my favourite – but Trent loves it and every time I take a box to a party or get together they always disappear quickly.

Ingredients:

  • 175g or 1 1/2 cups of  plain (all purpose) flour
  • 125g or 3/4 cup of rice flour
  • A pinch of salt.
  • 200g unsalted butter, softentend
  • 4 tablespoons of caster (super fine) sugar
  • Extra caster sugar for sprinkling on the biscuits when they are baked

Directions: 

  1. Preheat your oven to 190 degrees (or 375 degrees F).
  2. Line baking trays with baking paper.
  3. In a separate bowl sift the two kinds of flour together, add a pinch of salt to the bowl.
  4. In your mixing bowl cream the butter and sugar together until light & fluffy.
  5. Slowly add flour mix to creamed butter & sugar, gently mix until combined.
  6. Roll out dough into a disc and cover with baking paper or cling wrap. Place in fridge to chill for 1/2 hour.
  7. Now with a cookie cutter cut out shapes!! (If you don’t want to do this, you can make it in a slice tray and just pre-cut little squares into the dough every 3cm).
    I just think stars look pretty!
  8. Bake for 5 minutes, then reduce oven temperature to 150degrees or 300 degrees F & cook for a further 15-20 minute or until shortbread is a light golden colour.
  9. Remove from oven and sprinkle caster sugar over top while still warm.
  10. Cool on rack and then enjoy!

This recipe made about 60 small stars.

I hope you enjoy this recipe and if you make it please let me know.

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Elf on the shelf plan & Dec 1st box video!

Hey everyone,

Ok December is TOMORROW… I really thought it was just new years… But here we are almost at Christmas!!
Anyway – December 1st means…. THE ELF ARRIVES!

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Elf house construction has been happening for the past few days here…

Yes, if you remember from previous years – we have an elf, Kringle…
In our house we go all out, I love Christmas and love any excuse to be over the top festive!
I’m not really a fan of the elf doing naughty antics, so I plan more funny little set ups or he shows what we are doing for that day…
Tomorrow he will arrive and bring with him our 1st of December box full of lots of goodies for the children, I just posted a video showing the contents of the box – so please CLICK HERE to watch that!
Here is our monthly plan for Kringle’s time with us…

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Now I don’t follow this plan to a tee, it’s more an outlook for our December, so I can see what’s coming up and honestly we all have those moments as we just settle in for a good nights sleep in our comfy bed and then that thought pops into our minds – “darn it – I didn’t move the bloody elf!!” and you have to get up out of bed, half asleep and find the blasted thing and think of something on the spot.
So for me this list is an attempt to avoid too many moments like that.
It’s just our basic monthly plan, I can easily see what’s planned and what is happening at a glance and be inspired…
When I have funny set ups planned, that leaves me space to search for inspiration for a new setup or use one I’ve listed to the side… Also if we have something come up in December like a Christmas outing I’ll just work it into our plan…
I also have purposely left some blank days, that’s to give flexibility to swap things around and for last minute activities or outings!
I wrote this blog post last year with 5 tips to stay sane while our little festive visitor is with us… So I highly recommend you CLICK HERE to read that!

If you would like some elf inspiration please check out the hashtag #KringleTheScottsElf on instagram to see what I’ve done in previous years, or CLICK HERE to see it.

Also for December I write out our Christmas Bucket List and this also gives me ideas for what to do during the month…

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I find writing these lists gives me constant inspiration on what to do during the month and just helps my mind be a little less cluttered with trying to remember every tiny thing.
Do you have a rough plan for what you are doing with your elf or for the month of December?? What is your favourite antic your Elf got up to last year! I would love some inspiration for new cute/funny antics! Comment below or on my social media!
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Exist. Get in the dang photo!

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Hey friends,

Let’s talk photos… Family photos. Professional photos and just photos in general.
I love photos, always have. Ask anyone I went to high school with, I was “that” person with the camera at every party, school camp or function and to this day I take photos, daily. Yes, daily. Photos are my love language, maybe that’s why instagram is my favourite social media…
Recently on instagram I asked how many people regularly get professional family photos done, (regular being at least once every 2 years) 
The main response was NO.
And then I asked for responses on why you do or don’t get professional photos done… And I will get to them in moment, but right now I want to tell you why I invest in getting professional photos done.
Mainly so I am actually in them – as Mums we are so often the one behind the camera. I have countless lovely photos of the children and Trent with them, but not so many of me, heck even the pets have some lovely photos I’ve captured. But I want evidence I existed too in more than just selfies! But secondly because to me, they are like gold. They are so precious and I treasure them. And I know I will for the rest of my life, so they are an investment I’m happy to make.
A big reason people listed as not getting photos done was the cost and I agree some photographers charge way too much money and some deliver really poor quality photos – but there are awesome photographers out there who are affordable, offer great deals and do exceptional quality photos.
My tips for scoring good deals with photos is wait for times like spring or christmas when many photographers offer mini sessions, they are usually 20-30 minutes long, cost around $100 and you get 10-20 digital images… I like these sessions as they are cheap and easy.

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Our 2017 Christmas card.

Photo taken by Tina Ebenal Photgraphy.

Another way to justify spending the money on photos is write it off as a birthday gift for yourself. I did that last year. Or get an annual family photo done for the christmas card, print off and frame a few and presto easy & affordable christmas gifts for the grandparents! Or organise an extended family photo session, get everyone to chip in, then you can have full family photos, individual families and generational photos. That would be special and would make a lovely, thoughtful gift for parents or grandparents (birthday, Mother’s Day, anniversary etc) – because honestly those people never really need anything and that sort of gift I feel is so meaningful.
Another reason many people listed for not getting professional pictures done is because they do not like photos of themselves or their husbands aren’t fans of posing. Well, all I have to say to that is – do you think your kids or possible future grandkids will one day care if you think you looked good or not in a photo? One day you’ll be gone, sorry to be blunt – but we all die and all that will be left to prove we once existed will be photos. I treasure old photos of photos (yes photos of photos) I have of my grandparents, one day someone may feel the same way about your picture. Give them something more to treasure other than a selfie. And as for posing, well many photographers are happy to do lifestyle or more natural photos. You go to your session and positively interact with your family and the photographer just clicks away… Yes, they may give some direction but it isn’t so structured and posed as just sitting there and grinning. A good photographer should make you feel comfortable. I like both styles of sessions.

Our recent professional photos, taken by Tina Ebenal Photgraphy.
(highly recommend her, she is a Toowoomba & surrounds photographer)

Photos are something so special to me, I treasure them. I capture a photo of my kids daily and I document it for our family’s project 365. Basically I take one photo a day, everyday for a year, log it daily on an instagram account I have set up especially for this project and then at the start of the new year I make the previous years photos into a book. I print 2 off, one for each child. These photos range from professional images, to selfies and to photos I’ve taken on my good camera… It’s a mix of individual photos of the kids, family snaps, the kids together and with our pets… Just our day to day life, captured & documented…

To my Mum friends, I want to encourage you to be in the photo. Get in them, don’t shy away, you may not love the photo of you – but I promise you one day your kids will treasure that photo and so will you. Very soon our little loves will be grown, they’ll be busy with their own lives and we will have our photos to look back on & remember when we were their whole world… And then we will be gone and all they’ll have is those same photos. And no one knows when that’ll happen, so get in the photo. Exist.
And to Dads, take more photos of your wives! Pick up the phone and snap a photo of her sleeping in a bed with kids sprawled everywhere, take the photo of her comforting a teething baby, pick up the good camera at the birthday party and take a photo of just her and the birthday kid or you take the camera on christmas morning and snap a shot of her with the kids or you surprise her with a voucher for family photos, even if you hate them… She’ll fuss and complain and say her hair looks silly, but just take the photo. It matters.

And that’s the point, you matter. Photos matter, memories matter. One day our future generations will want to know us, give them something. I wish more than anything I had more photos of my grandparents… Something to show my kids and for me to see them – to see a glimpse into their lives back then… I use to love when my Nin would show me old albums of the family, I loved sitting at the kitchen table and seeing the black & white and sepia toned images and having her point out who was who and telling me the stories behind each photo… I promise you one day someone will want to see a photo of you.
Investing $100 into a photo session for some lovely photos you didn’t have to set a self timer for I feel is money well spent, but if you can’t justify spending that money and I understand not everyone can, ask a friend with a camera to snap a photo and then do the same for her family. Or if you and your family are out somewhere all dressed up, ask someone to snap a photo of you all, try and use a good quality camera if you can! Heck, you don’t even have to be dressed up, just grab your tribe, stand in some good lighting, throw someone who isn’t a family member a camera, all huddle together and smile.
Get a picture somehow. But I do highly recommend investing in professional photos at least once every 2-3 years.
Bottom line is, just get in the dang photo! Be present, exist.

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Our story with Kawasaki Disease.

Our story with Kawasaki Disease.

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Kawasaki’s disease.
Ever heard of it before? Nope, me either – it’s uncommon, but it’s serious and I feel more parents should know about it…
Please read THIS FACT SHEET to learn more (seriously, click that and read it, learn the symptoms)
This is a disease that should be on every parent’s radar. It is noncontagious but it’s very serious and needs treatment in under 10 days to help reduce the risk of long term damage to the heart.
Let me tell you our story with Kawasaki’s….

Saturday the 20th of October – LuLu’s party day, we woke up and our little man was just a bit “off” – nothing major, just grumbly and a bit clingy. He enjoyed the party and spending time with his Nan, but he didn’t eat as much as normal and we all agreed it was probably due to a big molar he was cutting. That afternoon he started getting lethargic and that night was dreadful. He was awake screaming & he had a fever in the high 38c’s.
Sunday morning when we woke up he had a rash on his tummy, by the time we had finished breakfast and we changed his nappy again it had spread to his back. So off to the hospital emergency department we went.
The doctor thought it could be just a viral thing – possibly hand, foot and mouth, I didn’t feel it was that – but being a viral thing made sense – kids get those.
By 4pm that same day the rash had intensified, so back to the hospital we all went. This time a new doctor said it was a random allergic reaction, Tommy was given an antihistamine and then steroids.

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This was his rash just before 4pm on Sunday evening.

We went home after a few hours and when we woke up Monday morning around 6am the rash had faded and he seemed to be on the mend.
A few hours later before 9am, the doctor from the hospital called and wanted us to return, she believed it maybe scarlet fever. By the time we arrived at the hospital, Tommy had gone back down hill and the rash had returned. (The steroids and antihistamine had masked the rash temporarily) We were given a script for penicillin and went home. At midday he started vomiting, I contacted the hospital they said it could just be the combination of scarlet fever, high temperatures and medicine making him a little unwell. He threw up a few more times and then again after we woke on Tuesday morning and now he had diarrhoea. We took him back to the hospital.
This time he had a blood test straight away and a cannula was inserted to start fluids.

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His “bear paw” – his first cannula.

They ran many tests; blood cultures, x-ray and from memory I think they started a broad spectrum antibiotic. And they started organising transfer to Toowoomba either by ambulance or care flight – which ever could come first. Ambulance it was.
Dalby Hospital did everything they could for our little man and their level of care was great. I can’t fault them for the multiple diagnosis, from what I have read this is very common in the early stages of Kawasaki’s because the rash and symptoms continually change and the symptoms could be many different illness, it’s all a process of elimination. The doctors and nurses really cared for him and we are so thankful.
Before 2pm on Tuesday we were loaded into an ambulance with a lovely nurse, I’ve never been in an ambulance before so that was an experience and I sat beside him holding his hand for our very quick trip. Trent and Lucy followed behind.

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I sat in the seat beside him on the right and he slept most of the trip. Thankfully we got there very quickly.

We arrived at the base hospital in Toowoomba, we were told paediatricians were on stand by waiting for us – we weren’t seen at all by one, so there may have been so miscommunication. Tommy threw up all over me again while we waited. We ended up asking for a transfer over to the private hospital and drove ourselves there. We couldn’t watch him become more unwell and no one could tell us when he would be seen properly. The base hospital was very busy.
We arrived at the private hospital at 7pm and were given a bed and a private room immediately. That night our little man suffered through more blood tests and they had to put in another cannula. He was started on more fluids and antibiotics. At this point they were worried about sepsis, a few viruses and possibly meningitis. Those possibilities were terrifying. We were exhausted at this point it was a hugely long day, I believe Trent left us at around 10pm that night to go back to Dalby.
The next few days were a blur with lots of tears, I sat in a hospital bed scared out of my mind holding our little man who just slept. He didn’t want to do anything and he was so upset. I felt like a zombie and my heart was shattered. Days earlier he was his normal cheeky self. I was wracking my brain trying to think how he got sick and I didn’t stop praying for him to get better. Trent drove in each day to be with us.
Wednesday was a rough day of more tests and this was the day he started to swell up. His little body went puffy, his hands and feet were like little balloons and his eyelids were so swollen. He is normally such a petite little guy, in hospital he gained 1kg due to the swelling. And his eyes were so red and blood shot, they looked painful.
Thursday I remember he sat up and finally ate something, he ate a jatz biscuit and a lemonade ice block for breakfast and then some weetbix. That was a huge moment, he hadn’t eaten for most of the week except a small amount of yogurt on Tuesday – which I ended up wearing anyway. He also had to have another new cannula put in that day, his 3rd one.

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During all these days we were waiting on blood test results, monitoring him constantly, weighing nappies, measuring water and our paediatrician was conferencing with the Lady Cilento paediatric team and infectious disease management team. His rash continued to spread down his arms and legs and he remained so puffy.
Thursday evening the paediatrician asked me if I had ever heard of Kawasaki’s disease… I hadn’t. She and the doctors she had been speaking to believed this is what he had, unfortunately there is no test for this disease – just ruling out other possible problems and that’s what we had been doing. Eliminating other viruses and illnesses. Every test was coming back fine, well not fine. His inflammation levels were through the roof, the highest she said she had seen in such a young child, his kidneys and liver weren’t doing great and multiple other worrying results – but for specific viruses nothing was coming back. Throat swabs, nasal swabs, stool, urine, bloods – it showed no illness – but there was clearly something going on.
We were waiting on one more test result to come back before we treated for Kawasaki’s… The only symptom that wasn’t exactly right for Kawasaki’s was his temperature wasn’t getting over 39c, but it was in the mid-high 38c – but the doctors believe the steroids he had been given on Sunday evening were effecting his fever. Because even with regular panadol & nurofen his temperature would continue to be higher than normal and he felt so hot.
The test result still wasn’t back by Friday afternoon – so we agreed it was best for Tommy to start the treatment anyway. The treatment is intravenous immunoglobulin – so it was not dangerous at all for him to have. Trent and I sat with him while the treatment happened and we prayed so much that it would work.

 

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Receiving the IVIG treatment.

Trent stayed in hospital with him that night and I went home to snuggle LuLu.
Saturday he did seem to pick up, he was more alert and playing. He was actually playing with toys! He ate more and just seemed brighter. We were so thankful that this treatment had seemed to work, if it hadn’t he would’ve had another round of it and if that failed, then he would receive a lumbar puncture – but thankfully we avoided that.
I stayed Saturday night and it was awful. We barely slept at all and I feel it was because he was more alert, suddenly he was much more aware of where he was and he was scared. So that was rough, but understandable with the constant nurse checks and flushing of his cannula. He was so sick of being poked and prodded!
On Sunday 28th/October he was weighed and was back down closer to his normal weight, we were getting our tiny little man back and after more blood tests we were discharged. It was so wonderful to get back to our big blue house and our own bed.

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The paediatric ward we stayed in, we were taken care of so well and all the staff were beautiful – but I hope we never have to return.

We saw our paediatrician the following Thursday, she said one of his blood results showed possible glandular fever as well.
The poor little guy, Kawasaki disease, possibly glandular fever, teething with molars and the paediatrician also believes he could’ve had a mild case of viral meningitis (due to his very sore head & neck).
We had another round of blood tests today (Thursday 8th/Nov) to check again for glandular fever & a bunch of other things, just to make sure everything has remained ok in his little body and we hope the glandular fever result was a wrong one and he hasn’t had that.
At the appointment we also discussed how upset and unsettled he has been since coming home. He has really good & normal moments and then he will just melt down and he is so sad, he doesn’t like being away from us and some nights he sleeps well and others he won’t settle at all… She believes his stay in hospital has traumatised him and he is suffering from a lot of stress. He still is suffering body/joint pain, peeling hands, feet & lips and appears to get very bad headaches. So all we can do is love him through this, we cuddle a lot, we carry him and stay close to him, we are gentle, we do massage and just take things easy. From the reading I have done these symptoms and the behaviour is expected and normal after Kawasaki’s.
Each day is getting better but we still have 6-8 weeks to go until we know if he has come out of this ordeal ok. In that time frame he will get an ECG done in Brisbane and that is to make sure his heart is ok. Until that test he has to have aspirin every day.
This experience was horrific. I am so thankful his issue was treatable and he responded well to the treatment, we continue to pray that his little heart will be totally fine and we have faith it will be, especially because he received treatment before day 10.

I want to encourage you, that if your child is sick and you are given one diagnosis and then they worsen/change – go back. Keep going back until the treatment works or you see improvement. You don’t have to accept one opinion. We are our children’s advocates. We have to fight for them. I knew each time in myself when he needed to go back to the hospital and I didn’t care if it turned out to be nothing, I would prefer to be known as the over cautious Mother than regret not taking him or leaving it too late. If we had just agreed it was some viral thing and tried to ride it out over a week, I hate to think of what the outcome could’ve been.
Because even in hospital with constant fluids and daily antibiotics given through his IV, regular pain relief and routine observation they were describing him as flat and not improving. I hated hearing that at each shift handover, I just wanted to hear he was improving – but I knew he wasn’t but I also knew he was in the best place and was being taken care of.
This was easily the most scary and awful week of our life. One I wish on no one and my heart breaks for families going through worse ordeals than this, gosh I can’t even imagine it. I know we are fortunate that it was this and nothing more serious.
So what caused this? It is unknown, it could’ve been anything – most likely just a basic germ and his little body sent it’s immune system into over drive causing all of his arteries throughout the body to become inflamed. Prior to the Saturday he hadn’t seemed unwell or anything, so we are puzzled. But we are praying this ordeal is now over and his ECG will come back with good results.

This blog post was created to draw awareness to Kawasaki’s disease. If you are concerned your child has Kawasaki’s please go to your nearest hospital or GP. If your child has this and you need support please feel free to email me at modernwifelife31@gmail.com and I can connect you with a great support group.
I pray you never experience this disease first hand, but if you do, know you aren’t alone.
Thank you to so many of you for your genuine kindness, concern and compassion over the past few weeks.
We would appreciate any prayers or positive thoughts towards healing and good results.

Thank you.

Once again, please click on these links and educate yourself on this disease and share this post or those pages with any other parents you know.
Kawasaki Disease fact sheet from Royal Children’s Hospital Melbourne
Kawasaki Disease foundation Australia 

5.

Tomorrow she is 5.

FIVE!

I’m dumbfounded by that…

I still remember the moment I was handed her and I looked down and said “hi baby” and I was so scared and so in love. I had never held a baby so small before, she was perfect.

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I still look at her and I’m so blown away by how perfect and incredible she is. But in hospital those first few days I was a tiny bit more obsessed, I took photos of her ears & hands – wanting to remember every detail about her and still I don’t feel I have enough to truly remember every tiny thing. So I wish I could go back and relive it all again.


I remember thinking I was losing my mind because I could not stop sniffing her, even if I tried I just couldn’t stop. Everything about her to me was amazing and I didn’t even want to sleep. I laid there staring at her, absolutely exhausted but just watching her because she was the most wonderful little person I had ever seen.

The last 5 years have sped by at a rapid rate and it’s quiet depressing! I feel like I’m digging my heels in, trying my hardest to pull time back or at least slow it down. But I can’t. So I have to be present and ride this wave with her.

She’s so amazing, (I’ll probably say that 10 more times in this post), but she really is. She was a really easy baby and is a pretty incredible kid. I’m so thankful to God for blessing us with her. We are lucky parents.

She can be a typical little kid, but she’s also wise beyond her years and we can reason with her. She appreciates honesty and being told exactly what’s going or why something is happening. She is not the sort of kid you can say “just because” to. As her kindy teachers and I laugh about, LuLu likes being informed, knowing proper answers on everything from why the sky’s blue to how is bread made and 1000 other questions – daily…

She loves her daddy and brother so much. Her Dad can calm her in any situation and he has an amazing bond with her. For example, when she had her 4 year old vaccinations I believe she shed only 1 tear. She didn’t even flinch, Trent sat there with her and she was brave. Because her daddy was there and he told her it would hurt but only for a quick second and then she would be ok. She trusted him and was the bravest kid. That moment still makes me so proud. I love how close they are.

Sure she can be a typical little preschooler, she has a temper and will argue to make you see her point (no idea where either of those traits come from) but my word she’s awesome. Just a magical little girl that makes my heart burst daily.

She’s the light of our lives. From the second she arrived she bought with her joy and light into our lives.


She’s a force to be reckoned with and will fiercely stand her ground. She is a sweet little girl who will love on her baby dolls and play with her barbies and she’s a rough and tumble kid who loves the outdoors. She loves it when I paint her nails and she often asks to wear my lipstick, but gosh she’ll jump at the chance to go fishing or hunting with her daddy. She loves her brother more than anyone, she’s a beautiful big sister – but she’ll also get cross at him for messing up her toys, but then instantly will baby him again. She’s gone from having such little hair I worried if it would ever grow to having a head full of crazy & curly hair! She’s bold, daring and adventurous and loves to be challenged. She loves fairies and one day will love unicorns and the next day dislike them greatly. She rarely likes princesses, unless of course she’s with her best friend or thinking of her, because then her bestie likes them. She’s a kind and thoughtful little friend who generously gives out compliments and has a beautiful little heart. She loves to draw and paint, is so intelligent and has a great sense of self confidence. And also has amazing strength and athletic ability (didn’t get that from me). She displays empathy and also is great at being rational. She is such a level headed little kid that it shocks some people, but then she’ll prance off pretending to be a ballerina…
She’s a perfect mix of wild and sweet and I pray so hard she always keeps that fire inside of her. The fire that makes her hard to parent somedays, the one that makes me pray for wisdom on how to raise her, the fire that makes her question every single thing I do or say or tell her to do… That fire will make her a strong force to be reckoned with. I believe girls need that and I know whatever she chooses to do with her life that fire will help her be successful and no one will ever take advantage of her. Lord, I hope she keeps it. I parent her carefully – trying not to squash it out.


She’s a one of a kind daughter and gosh I’m thankful to God He chose us for her.

I am mind blown she’s about to be 5. Mind blown also that we have been parents for 5 years. Gosh I hope the next 5 don’t speed by so quickly.

LuLu, we love you dearly – you are the light of our lives and we are so incredibly proud of the amazing little girl you’ve grown into.

Happy 5th birthday. 💖

Love Mumma. x

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