Showing posts with label why God?. Show all posts
Showing posts with label why God?. Show all posts

Wednesday, 19 November 2014

Hope Out of Despair #3

Close to the heart.....

When bad things happen to things close to the heart, often we find that our dreams, visions and hopes all come crashing down with it.

Maybe its a difficult season, not tragic, just a constant uphill journey... we get tired.

Maybe its tragedy, our life and all we thought seems to go up in smoke around us... where do we look, how do we move on from here?

Maybe its sickness, ill-health, disease, disillusionment, depression, discouragement.....

Maybe we don't even know what it is...

The reality of life is that there are mountains and there are valleys. No one is immune. Every single person faces trials and challenges.

Its what happens in you, in your heart, in your mind and in your world as a result of the things inflicted upon you. Thats what actually matters.

The truth is, as hard as it is, you CAN choose the outcome. You CAN choose if this thing will mean defeat or if you will walk until there's victory.

Im not saying you dont feel the pain in the moment. Im not saying we ignore grief, our emotions, our feelings or at all pretend that things are ok.

I am saying we can't stay there forever.

We must choose to face, and embrace the season of grief, pain or difficulty in order to move from it into a new season. It may take a long time, but as long as you are still walking through it, keep walking.

If you bury it, you will carry it. And unless it is given opportunity to be healed, it will likely destroy you later in life.

Scientifically its being proven more and more that most sickness and disease can be found rooted in some kind of unforgiveness, bitterness, resentment or brokenness that has resonated within a person for a long time. Sometimes so long the person has forgotten its even there.

We have got to learn to let things go, to let oyrselves be healed and made whole again.

We were designed to be connected with other people, people we trust, those who love and care and help to carry us through (or at least hear us out) during all seasons of life. The good, the bad and the just plain ugly.

We were also designed to be connected to our Creator. A loving God who gave everything for us. And when everything falls apart, He is really the only true and completely faithful friend who can be relied on 100% of the time for 100% of our needs.

If we dont look to Him, we will likely be filling the gap with something or someone else who just cant be that to us.

We were designed to live whole. To not carry the weight of the world. To not carry bitterness, unforgiveness, resentment or pain at our lifes circumstances.  We can try really hard to overcome, but I think most often that we cant truly overcome in our own strength.

We need support and we need the help of Jesus.

So if I could speak to your world today I would tell you to seek Him. To ask Him to help. Even if you dont know Him or doubt His existence. Ask Him to show you who He is.

My life is a story of brokenness, repaired and rebuilt by Him. He is worth knowing. He LOVES you more than you can imagine and He has seen everyday of your life.

He is the only one who can truly "save" us or make us completely whole.

Have courage to try again. Don't let go of the things that you "once" dreamed of.

Walk wisely and sensibly, but get up and walk.

Have hope dear friend. There is hope for change. There is hope for the things you have let die.

While there is breath, there is hope for better things ahead.

Jeremiah 29:11-14a NLT

For I know the plans I have for you,” says the lord . “They are plans for good and not for disaster, to give you a future and a hope. In those days when you pray, I will listen. If you look for me wholeheartedly, you will find me. I will be found by you,” says the lord.

Much love
Arna x

Wednesday, 16 January 2013

All in perfect time

Today's the day.  I'm going to try and tackle the monster of a story, because I get asked all the time and I know that lots of people want to know.

Time has lapsed, and in time, you forget and are 'healed' of the agony that you find yourself awash in sometimes.  But I'm ready.

This is the story of Mr E, and his 11 week premature arrival.

While pregnant, someone said to me "everything about this baby, the day he is born and the name you give him will be significant."  I filed this away for the day sometime in December 2012 he was meant to arrive.

Knowing he was likely to be my last baby, things were going smoothly with this pregnancy until I hit about 22 weeks. I started to grow exponentially.  I went from being "small" to being "massive" in a short time.  Then it started... contractions.  On and off contractions, JUST like last time with Mr A (who was 6 weeks early).

They were painful, every well meaning person kept saying - "oh that's braxton hicks" you know, practice ones.  I've had two babies previously by this time.  I know what BH contractions are, and I also know these are NOT them.

I'm full of fear.  Absolutely terrified that my baby is going to arrive soon.  I'm 26 weeks pregnant.  I decide it's time to be as much of a couch potato as possible.  Lots of rest, extra sleep and being extra kind to myself. I'm reassuring myself that it's going to be ok and telling myself that I will carry to full term.

I'm 27 weeks, a visiting ministry comes through our church.  He says something from the front about a person having gone through a traumatic event, and now, being in similar circumstances, is feeling terrified that history is going to repeat itself.  My last baby nearly died.  He was premature. My heart is thumping and tears are flowing as I know that this is for me. I go up to get prayed for at the end.  I feel nothing.

I'm 28 weeks and I start having 4-5 hour long stretches of consistent painful contractions every couple of days.  I'm still paralysed in fear.

It's Friday night and I'm in Delivery Suite.I've had a killer back ache for a couple of days. The contractions are coming again and this time my midwife says I need to be monitored.  I had called her and all I could do was sob and tell her that "I know there is something really wrong".  She takes me seriously.  I spend several hours there.  The obstetrician then decides I need a foetal fibronectin test.  This, when negative, predicts with 99.8% accuracy that you will not go into labour in the next week.  It is negative.

I reassuredly jump into the car, confidently knowing I am not going to go into labour in the next week and that I do not need to worry.

Saturday the back pain intensifies.  I can't sleep for sheer pain.  This is not normal.  Lucky I have osteo booked for Monday I tell myself.

I'm one day off 29 weeks. I'm at church again and I decide I need to get more prayer after Friday nights episode.  I go to my precious friend and Pastor and ask her to pray.  I explain what is happening to my body.  She prays.  Fervently, a prayer like she had seen my heart fully and completely and hears heavens answer.  Mostly, she prays against fear.

Monday comes, I am 29 weeks and today I am trying to feel confident I will carry to full term.  I am not afraid.  I go to osteo and there are some things out of place. I leave hoping for the best.  My backpain turns excruciating and debilitating.  I figure it needs a day or two to settle, so pop a tramadol and go to bed.

Tuesday arrives.  I lazily get out of bed at 730am.  There is some bleeding.  I calmly tell Dave he wont be going to work and call my midwife, while packing a suitcase.  I know I wont be leaving the doors of the hospital for a while.  I arrive at Delivery Suite to a virtual roll of the eyes that says "here comes the hypocondriac mum to be again."

My midwife, still taking me seriously arrives.  She throws all the jurisdiction between doctors and midwives out the window and pulls strings to arrange a scan for me later that day.  I cannot get comfortable with my back.  I writhe and roll and stand and sit.  I am being monitored but it seems to show a non-event.  They doubtedely run tests and leave me to it for long stretches.  Ihad the negative test remember.

Scan comes and goes.  The sonographer tells me that there has been a bleed, that there is lots of fluid, baby is quite large and that my cervix has shortened slightly.  I am concerned.  I dont know what to make of this.  She tells me she will prepare a report and have it sent to the doctor.

I relay this to a staff midwife who confidently tells me I will not be going far, I will be closely watched from the hospital and they will closely watch my babies growth.  I understand this.  The obstetrician doc comes and reassures me, the blood seems to be an old, now healed bleed.  I am weakly confident.  She leaves me to await the scan report.

Within the hour, contractions resume.  This time they seem a bit more hard and fast.  And they seem to be getting worse... I hesitate and lie there trying to work out what is happening for over an hour.  I then decide I better let them know.  They come in to the sound of my buzzer, where I declare that contractions have resumed but feel more serious this time.  They decide to check and I am now 2cm dialated and fully effaced and therefore in labour.

They immediately commence steroid treatment to try to stop labour and book a helicopter.  I'm going to Auckland.  The in-laws have our kids, so hubby rushes home to grab supplies, bottles, blankeys etc to get to their house so that they are ok for the night.

The steroids arent working.  And baby is breech.

I am loaded onto a very uncomfortable stretcher and whisked off to meet the chopper on the roof.  My hubby is no where to be seen.  He is met at security and delivered to the roof of the hospital.  He is there waiting as I come around the corner. <enter sigh of relief>

In the chopper I think to myself that this may be my only ever chopper ride, I better enjoy it.  The view was beautiful.  I wish I wasn't in labour.  The contractions seemed to have eased off a little.

I arrive in Auckland to a very organised Delivery Suite, where they immediately load me onto a bed.  The contractions have resumed hard and fast.  They (finally) offer me gas.  This is the best feeling of the day as for the first time in a week my back is not bothering me.  I have IV lines inserted into both arms.  One for a drug to help babies brain.. magnesium sulphate perhaps.  This is a four hour infusion and they hope that they can buy enough time for it to come through fully.  They tell me this is going to make me hot and bothered.  I am happy with the gas and this does not phase me.  The other is for antibiotics and fluids.

I suddenly feel the urge to push.  I tell them this, to which they check and advise me that my waters are bursting but I am not dialated more than 2cm and that if I push and break my waters they will have to put me to sleep and get my baby out.  Lucky I have had babies before and therefore can control this urge.

Baby is breech, it is confirmed.  The anaethetist arrives and asks me if I would like an epidural.  I strongly decline.  He then bribes me by asking if I would rather be put to sleep when they get my baby out.... I strongly refuse.  He then says 'oh, so you want an epidural?' to which I agree.  While he prepares this I ask if I can have my baby feet first, they refuse.  I then ask if I am really going to have him today... they say yes.

I get the epidural in.   By this time the contractions are coming on top of each other.  They are long, I suck the gas, I stop for about 2 seconds and then another is coming and I resume gas-sucking.  The anaethetist and Dave keep telling me, "you need to breathe some real air!" typical men.  They do not realise that there is no let up at all.  It is like one big contraction.

Finally the epidural kicks in.  It is like heaven.  Whoever designed those is a legend.  I see why people rave about them, I cannot feel labour pain at all.  I can relax and be fully aware of what is going on, not spaced on gas.

The charge midwife arrives, she takes a look at me, and the monitor.  She notices something.  She says, "we need to get this baby out now" and I jump the queue of all other cesareans booked for the night.  I am rushed to theatre, which is smartly built into the Delivery Suite.

They check with some ice around my neck, can you feel this is icy cold...? yes.  Can I feel it lower, no.  Ok, she is numb.  They proceed with the operation.  I can feel the sensation, but have no awareness of what is touching me.  I can tell which organs they are moving around and what they are doing inside me.  Dave is gowned up and at my head.

They pop my waters and measure it.  3L of amniotic fluid.  Most normal pregnancies have between 1 and 1.5L of fluid.  This is probably a good reason why at 29 weeks I measured 37 and felt like I was 37.  They find my baby, get him out and he is taken away.  I ask if it is a boy, they tell me yes.  They say nothing else.

They are gone a long time.  Dave is still at my head.  I begin to wonder why he hasn't been taken yet to see our baby - they told me he was going to go with them.  They finally come and get him.

He brings me back photos of our son, wrapped in a plastic bag for warmth, with a breathing apparatus in his nose. He weighs 1660g. 3lb 9 oz. I later discover that he required resuscitation and he was quite deliberate about not breathing.  He has a mechanical ventilator breathing for him for the next day.

They show me the placenta.  We see that it looks very peculiar.  It gets sent away for tests. As they cut it out they discovered that it was abrupting.  If it had fully come away, bubba would have died instantly.  I would have haemorraged and may have died.



I am taken to recovery and then later, on my way to my room, wheeled past him.  He is tiny, but beautiful. Perfectly formed.  His head is about the size of a tennis ball. Maybe smaller.  His whole hand is the size of the tip of my little finger.

The next day, we name him Ezekiel David.  It fits perfectly.  Ezekiel means "God has strengthened" and David means "beloved of the Lord".  We had chosen this a few days before he was born.  We didn't know what was to come.  His name is significant.

For the next 2-3 days I am written off while I recover.  Sometime, I get up and go down to visit him in a wheelchair.  I sometimes hallucinate from the pain relief I am given.  I am on close watch in the maternity ward because of the haemorrage risk.  There is not even coffee on this ward.  The staff are kind, and show me where I can make coffee. I am about 200m away from bubba.

Bubba is strong.  He had a blood transfusion because of being extremely anaemic when born.  He had stopped getting blood from me.  He is on CPAP, a breathing device which keeps his airways inflated but adds extra oxygen as he needs it.  He is reliant on this for his survival.  He starts having one ml of expressed breast milk every few hours.  He begins to tolerate this quite quickly.



His brother and sister are down for a visit.  They are not allowed in Neonatal Intensive Care (NICU)to visit him at all.  I show them pictures.  They leave with their grandparents.  Bubba is in a stable condition.  This can change at any time.

His milk requirement slowly increases 1ml by 1ml.  I am expressing 3 hourly around the clock.

The team who delivered him come to see me.  This is about day 3.  Here I am told that he didn't want to breathe.  I am also told that the very same night they delivered a 29 week baby by cesarean - who died.  I cry.


I am surprised when the paediatrician tells me I can hold him at 3 days old.  I expected it to be weeks before I was allowed to hold him.  I get my cuddle on Friday 5 October.  I notice that his ears are stuck to his head.  They haven't grown enough to be separate.  He is so tiny.


Saturday arrives.  It is our 5 year wedding anniversary. Dave gets his first cuddle. I weakly try to stomach my usual favourite turkish kebab for lunch.  I can't eat it.  Dave has to leave for Whangarei and our older kids, I am alone.  I cry myself to sleep.  Bubba has lost 250g.  This is a lot when you only weigh 1.660kg.

Sun 7 Oct.  Bubba opens his eyes a tiny bit, and looks at me for the first time.  I cry.  Today is my hardest day.  I am full of emotional/hormonal baby blues, and the agony of the situation.  I get lots of visitors, but there is nothing like being in a foreign city, away from your husband and family with a sick baby.  For the first time I am buckled over in emotional pain and cry out "Papa, help me" - to God.  I have no other words.  I try to contain the big heavy sobs that are knocking at the door.

This buckling over in emotional agony and crying out "Papa, help me" occurs most days that I am alone in a big city from here on in.  I don't have anywhere else or anyone else to look to than my Father in Heaven, whom I know has everything under control and knows all things.

7 days in I discover that the placenta had a large growth on it, called a chorangioma.  It was 5cmx6cmx7cm.  I googled it.  I found out that this is the leading cause of maternal death in the world.  And that it causes sudden infant death in utero from heart failure. I also discover it causes all of the complications I was experiencing in my pregnancy.  I thank heaven that God knows best, and I realise that if Ezekiel hadn't of arrived on the day he did, we would of lost him, and probably me too.  I am greatful for life, but again I cry with big heavy sobs.  The day he was born was significant.  One day later would have been too late.

I am now off the ward and down in Ronald McDonald House Family Rooms, emergency accomodation for out of town parents with children in Intensive Care.  They feed me and are very kind to me here.  Ezekiel has more tests, and they all return normal.

He has a brain scan.  It returns normal.  I cry at the overwhelmed goodness of God who has kept him perfect in every way.  I realise that for many people the situation is very different.  I am amazed that Mr E could be 5 weeks earlier than his older brother, and be in a much better condition.



For three weeks Auckland City was my home.  I had visitors nearly every day.  I had coffee and food brought to me.  I had gifts delivered and friends arrive from my home town.  I was loved upon.  I spent a lot of time crying in sheer pain.  And crying at the sheer goodness of God to me.  I know it's going to be ok.  Most of the time I am happy.  I make friends with some of the nurses in NICU.

I pray in the Emergency Accomodation, for the families, for the children.  I see people take their children home well, and the accomodation empty out to half capacity at a time of year that this "NEVER happens".  I am pleased to know God cares for these people.  I am also faced with the agony that in this place, families lose their children EVERY day.  In one week, four children died out of the accomodation I was in.




We stayed as a family at Ronald McDonald house a few times.  This is an amazing facility that accomodates whole families, and is on the Hospital Site.  It meant Dave and the kids could visit me but I could still be with bubba.  It felt like home.  Each time my family leaves I am grieved inside.  I cry and cry and have to tear myself away from my husband and not look back.

On 22.10.12 they finally tell me that they have booked the helicopter for us to fly to our hometown.  On 23.10.12 after three weeks in Auckland we fly to Whangarei.  I was hoping for fine weather, but low cloud made for a not so fun ride and I couldn't see anything!

For the next almost six weeks we were in Whangarei SCBU (Special Care Baby Unit) where the focus was to keep feeding and growing him until he was strong enough to learn to breastfeed and then get ready to go home.

The process is painstaking.  Prem babies sleep ALL the time.  They are hard work.  I had to commute to and from the hospital everyday.  At first, by bus or reliant on rides because of the cesarean.  You just sit there, hold them, bathe them, feed them (through a tube in their nose going into their stomach), change them, cuddle them and wish for them to get well.  Some days are good days, some days are bad days.  Some days move forward, some move backward.  Some weeks show a lot of progress, some you feel like you have nothing to show.


People used to ask me where my baby was, not realising that prem babies have to develop on the outside all the things they would of had to do in your tummy between weeks 29 and 40.  All the while getting fed, digesting food, learning to breathe etc. Its a long haul in hospital.

He was on the CPAP breathing system for about 5 weeks, then another system for a few days, then he was breathing on my own.  The doctors all told me that I was "very lucky" to have my 29 week baby off oxygen before I went home, it doesn't always happen.




I expressed milk 6-8 times a day (through the night) for almost 9 weeks, in hope that he would breastfeed.

I made friends with the staff (again). Coming back into SCBU was like a welcome reunion after my previous child spent four weeks in there.  I was so glad to be back in my hometown.




Some days I had visitors, most days I sat next to my baby alone longing for the day I could finally take him home.  The greatest emptiness I felt was at an extended family dinner when I suddenly realised our entire family was there, except for Mr E - and when I left to return to the hospital, my heart broke.  That was the night before his discharge.

The day I went to stay with him to prepare him for home, I wasn't sure if he was really ready.  I decided that I would take out his nose-tube and forcde him to have to breast feed.  It worked, and two days later the paediatrician said I could bring my baby boy home.  I cried and cried.  She cried.  The nurse cried.




I could go on forever about the experience, but I don't think words could adequately describe what it is to have a baby so early, to not know whether your baby will make it through the day, whether today will be good or bad.  To be stuck in another city and reliant on the charity of others and their goodwill as to whether you will get company that day or not.  To be faced with the rawest emotions, the deepest heartache, the loneliest place in the nation (hospitals) and have to cling real tight.
To have to daily choose gratitude instead of the 'why's' or wondering how you got to this place.




I don't know how people do this stuff without Jesus.

We are indebted to the countless people who prayed for me, for Mr E and for our family. Those who bought us gifts, cards, food, coffee.  Those who visited.  Those who text, some every single day.

We are indebted to the people who followed their deepest desires and dreams and became nurses and doctors and midwives and professionals and saved our lives. 

Mostly, we are indebted to God, our Papa, who held us close and loved us and covered us completely with love during this time.

Traumatic and stressful as it was, for the vast majority of the journey, I was full of faith, full of hope and full of exceeding joy.  I didn't fake it once.  Sometimes I had to make a choice, but usually it was natural.  I cried only a few days, but I laughed every day.  I gloried and marvelled everyday in wonder and amazement at how good Mr E was, and therefore, how good God is.  With all the complications and everything that could of and should of gone wrong, I stood in pure amazement and wonder that I had a healthy baby and that every single test came back ok, clear, normal.

Sometimes I felt undeserving of such goodness.

I wholeheartedly believe that we were supernaturally carried through the storm.  I also believe that our previous experience with an early baby helped us to carry through.

We need to fight for our babies.  For the babies that are born, the babies that are unborn, and the ones that aren't even conceived yet.  We MUST fight for the next generation.  They carry the greatest legacy the earth has ever seen.  They carry destiny.  We MUST stand for them and on behalf of them.  Where they are non-existant we must find the courage to call them into being.  But we also must live with our children fully surrendered to the will and purposes of God.  They are not our own, they are His.  They have been given, lent to us for us to do the best we can to raise them, grow them, teach them and release them.

I want to testify that even in the most dreadful of circumstances, when everything familiar and that you hold dear is shaken, when you're in the furnace of life's trials and the heat is hotter than ever - you can stand, you can raise your head, and you can carry joy, hope, life and love in that place.  You can release those things into other people when you're in that place.  You can laugh.

I want to say that the day my friend and Pastor prayed for me, just before I had him, neither of us had any idea what was to unfold.  In the process of labour, delivery and the weeks that followed, I did not feel an ounce of fear once.  If I felt like it was trying to knock at the door, I would suddenly think - if God made Him come on the perfect day, at the perfect time and preserved his life - He WILL come through for this too.  I was confident and fully able to trust that everything was going to be ok.

People credited to me that I was 'such a strong woman' - I don't credit that to myself.  The only place I credit that to is because I know where to find my strength when I face a struggle and a challenge.  I have a God who is much, much bigger than life's problems, situations and circumstances.  And I know Him.

I cried a lot, but I didn't cry in emptiness and despair to nothing - I cried to Him, and He came to me and held me and took care of me.  He put people around me to love me and help me and encourage me.  He anchored me.  I had never known Him before this better than I know Him now.  You get to know Him in a trial like you couldn't know Him any other way.

My prayer for you, is, whatever you are going through, wherever you find yourself today, whether you are in love with life, or whether you are at the dregs and don't know what you have left to hold on to - that you would truly find Him in that place.  He longs to be found by every person, and if you really want to find Him, you will.  I dare you to ask Him - if you are real, make yourself known to me.  That is a prayer He simply cannot resist.

Afterall, He knows you and He made you and He sees you anyway - good and bad, everything about you.  He is not surprised by you in the slightest.

I am more than willing to share with any one at any time if they want to know more.

For now, may you find the victory and freedom you are searching for in your life and your family.

Much love
Arna x












Saturday, 30 July 2011

6 weeks too early, not a day late...

I know this post has been well awaited, and it's going to be well read.  Before I begin - I will add a disclaimer -

much of this is very difficult for me to show in a public arena, and to "talk" about.  This post will probably be long, but I'm keeping with who I am in being honest and real.  There are pictures - they are not all nice to look at.

Welcome - Aiden Harris.  Who arrived to our family - on 3 July 2011.  6 and a bit weeks before his due date.



What can I say - but I knew it.  I knew he was going to come early.  I just didn't quite expect the journey to follow.

Most of those who know me, know I LOATHE being pregnant.  I could honestly quite happily skip that stage and go from not pregnant to the day after delivery quite happily.  So when I woke up on that Sunday with some dull ache, and then contractions arrived - I was just a wee bit excited.

I shrugged it off - because over the 3 or so weeks prior, I had multiple false alarms.  I was hospitalised 2 weeks earlier with "labouring" contractions - that slowly eased off overnight.  So I knew that each day counted as one step closer to home.

The labour - well, it was amazing.  Very different from my first experience.  I was very relaxed and quite enjoyed just breathing through the process.  I left church a bit early because I was uncomfortable.  Thinking I was going to be in hospital for the night again - I grabbed pjs and a few other things.  I threw in a feeding bra "just in case".

I was not afraid, but was chewing back on steroids every 15 minutes and being jabbed all over.  You see, they were trying to stop my wee boy from coming quite so soon.  Things continued to progress and my midwife decided to bring me in some gas.  I quite enjoyed that experience too.  It was all a bit blase because I wasn't supposed to be having this baby, but I started to think "gee, if I don't have him today - this is going to suck - I'd have to do labour twice for ONE baby!!"

I was given the "last resort" pill, which either stops your labour or you are declared full blown.  It was a bit late - I was full blown.  A short time later I told my midwife that "I'd be ready to push soon".  She checked and I was nearly fully dialated.  After this, I don't remember much.  Apart from that I was begging them to break my waters.  Other than that after about 10 minutes the alarm was pressed, the paediatricians rushed in the room and my son was born.  He was promptly removed and given some oxygen to "pink" him up a bit.

I was given a 5 second glimpse at him wrapped in a towel, and then he was transferred to the Special Care Baby Unit (SCBU) because he was labouring a bit with his breathing.

My established labour was less than 2 hours.  I was happily breathing through it all and texting my friends at 12.50pm.  I gave birth at 2.30pm.

I was in shock for about 3 hours.  I couldn't believe I had just had him.  I hardly got to see him - it all felt a bit strange.  I finally showered and gathered my things, then went to see him.

He was the cutest wee thing ever.

Day one he was doing quite well.  We all were.

Then came Monday.  The Doctors then told me that he had developed a "condition".  Basically, the short is - Aiden's body was delayed in converting from using the placenta for oxygen to using his lungs for the circulation he needed.  No visitors, and I wasn't allowed to touch or talk to him for at least the next 24 hours.  I still hadn't even held him.


Some of our darkest moments...



The gadgets above are as follows:
  • oxygen + air in his nose - keeping lungs inflated and providing extra oxygen to enable his body to get enough for circulation
  • aspirate tube down throat into tummy - to enable them to suck out mucous and remove breast milk to check for digestion
  • wires on chest/tummy - recording heart rate, oxygen levels and breathing rate
  • IV line in his arm - for fluids and later, for fluids with "extra calories"
  • 2 x wires in umbilical cord - 1 for monitoring blood pressure and taking blood. The other to "feed" him with (among other things).
  • wire on foot - measuring oxgen saturation levels

    They did consider transferring him to Auckland via helicopter.  They were seriously concerned about his health.  They didn't relay to me quite how bad it was until he was 'well' (about 10 days later).


    Not only did he have a condition - but he couldn't tolerate any breast milk at all (so he lost a lot of weight).  On the Wednesday, he started having serious apnoeas (holding his breath for long periods).  He would do it several times in a short space.  They got even more concerned about him.  He hated any stimulation.
    With his dummy ^^  the only comfort he had
    He was lying on a table, vulnerable to all the elements.  Every time a doctor walked in the room, or there was a new voice, or someone got flustered - he would get distressed.  He would handle this by holding his breath again.  He would cry and grizzle and look like he was trying to leap from the table.  All the while I just had to sit there and watch him - because I wasn't allowed to hold him or hardly touch him.

    To be honest, for the first week, I sat next to his bed - and cried. And silently prayed and desperately hoped and willed for him to keep fighting.

    Having a break from some of the wires ^^ and loving it!


    That night, finally - at midnight, the nurse decided to shift him to an incubator to try to help him handle all the noise etc.  She landed him in my arms for the first time.  I said to her through tears "am I really allowed to hold him???"

    From that moment, he never held his breath again.

    "Sunbathing" - being treated under the phototherapy lights for jaundice.  Wires slowly coming out.


    Each day he progressed.  His tube down his mouth, turned into one down his nose.  This was to feed him.  He was far too little to know how to suck properly, so there was no hope of feeding him breast or bottle for a while yet.

    He started to tolerate 1 ml of breast milk every 2 hours.  Yes, 1ml.  Slowly over a period of days that increased to 2mls, 3 mls until it was at his total of 59mls every 3 hours.

    2 and a half weeks on, he started wanting to suck.  He was still very sleepy, so he'd have a short breast feed, then a tube top up, then sleep for the rest of the day and night.

    I spent 3 weeks waiting for him and teaching him how to suck so he could feed.


    After 12 days, I got sent home from the hospital without him.  I commuted each day to be at his side, feeding him through a tube and expressing my milk every 3 hours.  Coming home without him was absolutely heart wrenching - but my family needed me at home.

    Finally, another week on, I was being called back in to the hospital to stay with him and get him ready to go home.

    Then, after an episode in ED, I got readmitted onto the surgical ward for myself with severe mastitis.  I was in agony (I even thought I might of had meningitis again).  They were going to operate, but decided first to aspirate - the treatment involved needles in places no woman wants a needle.

    IV antibiotics for another 5 days and apart from my baby all that time - he went back to tube feeds.

    I was devastated.

    Come the Monday, I was awaiting a further diagnosis from the surgeon and the "next step".

    The prayers of many faithful people meant that the surgeon checked me - and it was decided I didn't need any further treatment.  I begged him not to continue the IV antibiotics but to let me go with oral ones so that I could go back to Aiden.  He agreed.

    I spent the next 4 days re-teaching my sleepy boy how to breast-feed, and to wake for feeds.  Monday he had his last feed from his nasal gastric tube.  (He had been pulling it out every day for about a week).

    Finally no NG tube in his nose ^^

    Tuesday he was weighed. He lost 15g.  That's normal for a baby converting from tube feeds to sucking (using energy) for feeds.

    The condition for our discharge was that he had to be all breast-fed and put on weight.  Thursday was the next opportunity for weigh in.  Thankfully, he succeeded in putting on weight and, after 3 and a half weeks in hospital, we came home!

    My wee poppet, in his short life, has already battled death twice.

    I am so greatful that God is my rock, and my keeper.  I have no other.  At one point in my labour, I was SO aware that God was there.  It was like Jesus had just literally walked in the room.  This kept me while I sat at Aiden's side - helpless, but knowing God was willing him to live more than I was.

    Heading home ^^


    Yes I've cried millions of tears, I've asked mega questions and I've come pretty close to the edge.  I've pleaded before God for "no more" and I've cried in my mum's arms telling her I can take no more.  It's been a rough 4 months for us.  But I can sit here and write that I know we are on the side of victory, because Victory Himself is on our side.

    There is still ongoing things with him.  Aiden is well, but must be protected.  He is still little and vulerable.  So, for a while - I will be hibernating.

    I am looking forward to watching his little life unfold - because I know he is destined to greatness.

    For now, back to my crying baby ;-)

    Monday, 11 April 2011

    I WILL LIVE to tell the story...

    Ps 118.17

    I will not die, but I will LIVE

    to tell what the LORD has done......

    Almost three weeks ago, I lay on death's doorstep.

    It started with a headache.  So severe I could not get out of bed.  I was so tired, but could not sleep for the pain.  It was so intense, I failed to even put 2 & 2 together with any other symptoms my body was facing.

    The rest - which I realised while being questioned by my GP was, I had such a stiff neck, I couldn't stand any light, I was running a high fever but freezing cold, I couldn't stand to straighten my legs, I had to lie down.  I felt incredibly nauseated - even drinking one sip of water was enough to make me want to vomit.

    The pain I was experiencing - was MUCH, MUCH worse than labour.  I visited my GP - hoping for a jab in the butt to be sent home to get over my "migrane".  Of course, being pregnant - they couldn't give me anything.

    Next I knew I was being checked head-to-toe for a rash and sent straight to ED at our local hospital.  The GP phoned in advance and sent me with a letter - so I could be seen "immediately".

    I arrived, could hardly walk in the room, let alone tell them my name or write.  They took my letter and I sat down.  The room was busy - full, of really unwell people.  I saw the nurse, who checked me and told me it "will not be long" before I got to see the doctor.

    Three and a half hours later, my husband, mum and miss "alsmost 2" at my side, I was still waiting.  I lay on a small couch in the busy main corridor of the hospital - because I could not bare to be upright.  I kept my eyes shut and periodically faded in and out of "awareness" - which I figured later was consciousness.  I shivered with cold and couldn't stand any noise.

    They called my name.  By this point, I could barely stand, nor walk.  I could not control my body in the least.  I was beginning to convulse, hyperventilate and cry - at the same time.

    The nurse ordered blood tests be done immediately, drip was inserted because I was severely dehydrated.  My fever was running high.

    The doctor was in shortly after, and I was checked all over and asked a multitude of questions (for the 4th time).  He left to talk to his boss, and the nurse stayed with me. 

    The first few drops of morphine - were literally like heaven (haha).  For the first time, I felt much less pain and could open my eyes.

    I sobbed and sobbed - "what about my baby....??"

    The doctor returned.  I had meningitis.  He suspected it was viral meningitis due to some of the onsetting symptoms I had, he was happy to diagnose me without any futher tests. 

    He told me that they cannot treat viral meningitis.  It is also not considered "dangerous" like bacterial meningitis is.  They would give me some pain killers and send me home, that I would have a headache and be sick for a couple of weeks and then start to come right.

    But I was given a choice.  Little did I know - the choice was likely to mean the difference between life and death.

    If I left, and got worse, I had to come back to ED.  And join the back of the line in waiting again.  I would not have returned.  The wait was too agonising and traumatising as it was, let alone to do it a second time.

    He said the other choice, was to have a lumbar puncture done - which would actually diagnose whether I had bacterial or viral meningitis.

    I felt incredibly compassionate towards the other very sick people who were in the waiting room, waiting for a bed in the ED.  I felt swayed to go home.

    But deep inside me somewhere - I knew something just wasn't right.

    So I asked for the lumbar puncture.

    The LP wasn't as bad as I expected (or had been told by others).  It's not a nice thing to have done, but I did not care for fact that it would help make me better.

    A couple of hours later, I was diagnosed with bacterial meningitis.  Much to the doctor's surprise.  An ultra-sound was done to check baby - and there was lots of movement and a perfect heart rate.  *Sigh of relief*

    Mum had taken miss "almost 2" home for dinner and bath, hubby then had to leave to pick her up and get her to bed.  Later, without warning, I was collected by two people with plastic gowns from head to toe, and masks on - and delivered to my room.  The masks and gowns were part of my life for two days - until I was no longer "contagious".

    I felt like an enemy of the human race - biological warfare waiting to be released or something.  At one point, I had five medical staff in my small room, peering at me from behind their peculiar costumes.

    For the next 8 days I lay in hospital - in a room completely dark.  My visitors actually thought I was sleeping - but I couldn't handle even the faintest light.  I could not read or write.  I could not even bear to look at pictures.

    I could maintain an upright position for only 5 minutes, before suffering excruciating pain and needing to sleep.

    I never knew how the wriggles and kicks of a tiny baby could be such a relief.  The baby is alive.  But even more, I am alive.

    I had meltdowns in the middle of the night.  I had panic attacks in the night (and day).  I felt depressed and alone, but any visitors made me physically and emotionally exhausted.

    One morning, I couldn't even open the small packet of jam to put on my toast.  I called the nurse, in tears, who opened it - then I couldn't even use my knife.  The sheer frustration of wanting to do a simple task, but physically not being able to, was terrible.

    I desperately wanted my God to come and make me well, sometimes I wondered why all this had happened and where He had got to.  But I knew He would never leave me, nor would He make me sick, or "allow" me to be sick.

    People came to pray for me, my family was desperately praying for me, my friends were desperately praying for me, my church was desperately praying for me - people I don't even know were crying out to heaven for me. 

    And I can truly say that I am SURE, if it weren't for God, I would have died.  I am greatful for the prayers of many warriors who cried out for me in my despair.  And who are still crying out for my total healing.

    I finally came home.  Still in incredible pain, afraid of light and unable to do most things.  My arms were like those of an addict from all the IV's and blood tests.  My husband, looked glazed and stressed.  His busiest time with his work, an incredibly ill wife and a demanding child.

    Then came the helps.  Dinners cooked and delivered every night.  Babysitters, house-cleaners, people just to sit with me.  Vouchers for special trips to a cafe.  What stars I have for family, friends and wider church family.

    Each day since coming home, I have improved.  I can now read and write again.  I can stand light although sometimes get a slight headache or uncomfortable feeling.  I am barely in any pain apart from my back and tailbone are still quite sore.

    My brain is sometimes still slow, speech sometimes slurred and occasionally loud or sharp noises still hurt my head.  I am off balance - which makes me afraid of large groups of people or things like crossing a busy road/carpark.  I cannot hear or see as well as I could.

    I recognise that there is not only the physical damage on my body (which I believe I will make a FULL recovery from), but there is also a lot of emotional trauma which I am working through.

    BUT...

    I am greatful.  I am so greatful to be alive that the very thought moves me to tears.  I am greatful to be able to hear/see and do most of the things that I used to.  I am greatful to tuck my sweet little princess in at night, and experience the joy of her laughter - even just one more time.  I am greatful to look my husband in the eyes and tell him I love him - even just one more time.

    I am greatful for all the people who have been pouring themselves out for my benefit.  Because they believe in me being well again.

    I am greatful to be given another chance at life - because I sure didn't live the last chance I had as much as I wanted to.

    I am greatful that I serve a God who WANTS to heal people.  Who DELIGHTS in healing the sick and doing miracles.  A God who is real, and who loves fiercely.

    I know, that as I lay there fighting for my life, in the darkest moments - He truly sat in the chair next to my bed keeping watch.  Willing me to rise again.  Willing me to live.

    x

    Thursday, 25 November 2010

    Questions in crisis....

    I was going to post a whole lot of pictures about my week, but I will leave that for another day.

    Today, our Nation is mourning a great loss.  29 good men have died in the Pike River Mining disaster.  A tragedy.

    In times like this, words cannot really describe the anguish that the people are feeling.  Words do not console.

    As a Christian, many people turn to you for answers.  People ask questions like - "where was God?", "why do bad things happen?", "why didn't He stop it from happening?"

    While I cannot answer those questions, and tears fill my eyes each time I get asked another - I can offer something.  God's heart hurts more than anyones over this loss.  He grieves, because He too has lost.  He does not will that people should die young, nor does He want people to die before knowing Him.

    Anger and questions and doubts and worries are all a part of the grief process, and they are all ok.  Let grief come.  My prayer is in the midst of this horrible storm, people will look and see how big, how loving and how great God is.  He is the comforter.  He can give new hope.

    My heart, prayers and thoughts are toward the whole town of Greymouth right now.  You are all hurting and we as a nation are hurting with you.

    I feel there is an appropriate song for this tragedy in our nation:-

    I love the bridge, very relevant...

    Fee, Everything falls apart







    You said
    you'd never leave or forsake me
    when you said,
    this life is gonna shake me
    and you said
    this world is gonna bring trouble on my soul
    this I know

    When everything falls apart
    Your arms hold me together
    When everything falls apart
    You're the only hope for this heart
    When everything falls apart
    And my strength is gone
    I find you mighty and strong
    You keep holding on
    You keep holding on

    When I see
    Darkness all around me
    When I see
    That tragedy has found me
    I still believe
    Your faithful arms will never let me go
    and still I know

    When everything falls apart
    Your arms hold me together
    When everything falls apart
    You're the only hope for this heart
    When everything falls apart
    And my strength is gone
    I find you mighty and strong
    You keep holding on
    You keep holding on

    Sorrow will last for the night
    but hope is rising with the sun
    (it’s rising with the sun)
    and there will be storms in this life
    but I know you have overcome
    You have overcome

    x