Luke: What you didn’t know

You were too young to understand

The world into which you were thrust

You were used to holding Mummy’s hand

And having her full attention

.

The arrival of a second child

Was not something you knew

And the process

Was not something for which we could have prepared you

.

You didn’t understand the constant tears

The medical appointments

The bleeding at 18 weeks and the regular fears

And that was just the pregnancy!

.

You saw your Mummy doubled over in pain

And you helped rub her back

At 36 weeks as labour began

.

You didn’t know you were saying goodbye for many days;

That this little brother would take away your Mummy

You didn’t know why hospital became a second home

That Mummy seemed to always reside at

.

We couldn’t explain medical terms to you

Things like special needs and disabilities

You didn’t know what heart surgery meant

Or that we used to count your brother’s every breath

.

But what you NEED to know

Is that despite all these things

You were never far from Mummy’s heart

And her thoughts were always for you

.

Her heart was with you

As you went to bed at night

Tucked in by your loving Gran

Her thoughts were with you

As she drove to hospital

And unpacked yet again

.

She cried for you

Many nights

Wondering if you were okay

And what she could do to help you

.

The world into which you were thrust

Was not a fair one

Nor was it just

.

Mummy had no idea having a second child

Would come with so much unexpected pain

.

But what you need to know

Is that your Mummy loves both her boys dearly

And will always protect you and love you

Some things Mummy can’t control

Even though she will do her best

To tuck you close and wipe away your pain

.

But one thing Mummy can control

Is that for each of her boys,

She will always, desperately love you

And hold you in her heart

And never let you go.

.

Your Mummy loves you

And is sorry your life began with so much struggle

She would change it if she could

And take “special needs” away from our vocabulary

.

But Mummy just has to trust

That God has a plan

Even though she can’t see it

And believe that we are just the family

For your little brother too,

Just as we are the right family,

Chosen for you.

Brain Damage


Standing at the kitchen bench

Surrounded by medicines and heartbreak

A future unquantified

Broken only by the constant repetition of medication and struggle


This was not the future I anticipated

It’s not even a future I want

Will my son be like this forever?


Despair settles like a cloak over my shoulders

Anguish spreads its tentacles throughout my veins

A son that doesn’t even register my presence

When I go to collect him from his cot


What happened to the world of happy children?

Who respond with smiles upon seeing their parent?

Who look up eagerly and stretch out chubby hands?


My future yawns in front of me

Cavernous and never ending

The world of disabilities

Feels like a chain around my neck


I can see no way forward

No way through

All I know is that to keep going

Is going to take everything I have.

I can honestly say that these weeks were the hardest of my life. Being told my son had infantile spasms and had already sustained “significant brain damage” – there are no words adequate to describe those emotions. Being told next by the doctor that “left untreated, he would die a slow and painful death” are words I will probably never forget. This was me staring at my younger son in his hospital cot, wondering if he would survive – or not. And if he did survive – in what capacity would that be? What kind of future did he – and we – have ahead of us now?

When hospital becomes your home

For those who’ve wondered what being in hospital 74 days is like…..

It’s waking up in the morning, not because you want to, but because you have people in your room and you only have so long to shower and dress before all the doctors arrive.

It’s not sitting on the toilet seat… for months… because who knows who else has sat there and when it was last cleaned?

It’s not knowing what’s on the menu for that day – or actually, pretty soon it’s knowing EVERYTHING on the menu – ANY day!

It’s finding yourself in a hallway discussing your toiletry habits with a middle aged, black African male nurse, before you realise how institutionalised you have become that it just felt “normal” – “Yes, I’m just racing to have a quick shower, then I’ll be back in the room and we’ll change his nappy to weigh it, strip him down, weigh him, give his morning meds and prepare for the doctors to arrive”.

It’s being woken up all through the night…all the time… with lights on… with nurses being so rough changing your son’s nappy they wake him and you… with monitors alarming and you’re flying out of bed to check them… with nurses shining their cell phone lights in your face… with helicopters coming and going all night… with rubbish trucks slamming over the jutter bars through the night… with cleaners on machinery in the halls at 5:30am… with other screaming children… with nurses putting a hand on your shoulder and startling you awake because they want you to express another 5ml for the next feed which is in three hours, not knowing they just woke up a bear who was in desperate need of sleep…

It’s not knowing how to walk one more situation of conflict with staff who often don’t seem to know the hell what they’re doing… like the nurses who openly admit they haven’t read your son’s notes. They don’t know he is a highly complex cardiac baby and so it’s listening to nurses flood the room looking at his oxygen saturation going, “It shouldn’t be dropping this fast.” And you’re sitting on the bed finally succumbing to tears because you’re freaked out of your mind at their reactions, wondering what’s going wrong – until you find out – hours later – that the nurses didn’t know he was a cardiac baby so put him on oxygen when he never should have been. And you realise in that moment to trust no one. Unless they seem really knowledgeable – and have actually read your son’s information file!

It’s getting used to telling nurses information or instructions – and having the opposite happen… fifteen minutes later.

It’s learning to tell your story… over… and over… and over… again.

It’s learning to speak “medical speak” like you know what you’re talking about… although… pretty soon you do!

It’s talking to eight different specialist teams and realising most of them see YOU as the central point – “What did the cardiac specialists say?” “What did the respiratory specialists say?” You realise it doesn’t matter how overloaded, how overwhelmed, how exhausted or frankly even how terrified of your son’s health you are – you are the central cog seen as the fount of constant information at everyone else’s mercy – you don’t get to choose how often you have these conversations, or when.

It’s learning no time is EVER your own. You don’t control who walks through your room. Whether you like them. Or not. Whether anyone will ever actually ask – “How are YOU?”

You learn not to bother with things like moisturing your hands or flossing in your room at night, because you should only do them if you’re willing to have an audience at a split second’s notice.

It’s hearing things like, “Your son has heart failure. Your son has fluid build up on the lungs. Your son has pneumonia. Your son has combined bronchiolitis, parainfluenza and rhinovirus.”

Or my personal favourite – “We’re going to break your son’s bones and stop his heart in heart surgery.” And you stare at your husband, neither of you showing any emotion. Your husband suddenly jumps up to stare at your small, innocent son, struggling on a cot just to survive where he is fed continuously through a nasal gastric tube.  

And you know there’s a chance. There is a chance this could be your last night with him. And you can’t even begin to process that.

It’s holding back the tears and emotions until the surgeon leaves the room and knowing the countdown to surgery the next morning has begun.

And then –finally – letting yourself breathe… and cry. And then it’s watching while your son vomits bright yellow bile, and the nurse you hate walks in. She sees you, and your son, and flippantly states, “Oh I wouldn’t bother worrying about a little thing like that.”

And you’re staring at her, going “Do you know my son has HEART SURGERY tomorrow?”

“Oh, yes.”

And you have no energy left to care that this woman doesn’t have a clue. And you are so spitting angry at her insensitivity that you have to walk out of the room, and the evening you envisioned of holding your son close and talking to him has just evaporated, because you’re too angry to want to taint your son with your emotions the night before you could lose him. Knowing that any “little thing like that” could change whether your son HAS the life saving surgery in the morning, as so many other “little things like that” have changed the surgery date so far.

It’s the constant terror of not knowing… if your son will survive… if your son that has been SO strong so far, can continue to be strong, when he has given so much already and gone through so much…

It’s wondering for yourself. If YOU can survive this, when YOU have already seen and watched too much.

The 50 odd blood tests. The people squeezing your little’s baby delicate heel like it’s a stress ball, determined to ooze out enough droplets of blood. Then finding they squeezed it TOO hard and the blood separated (don’t ask me) and so they got a false reading… and they have to do it… again… and again… and again.

It’s fleeing the room because you just can’t watch one more traumatic procedure on your son. You can’t comfort him one more time as they hurt him (while trying to help him) because your own heart is breaking in two watching this happen, over… and over… again.

It’s wondering when things will ever get easier.

And finally, not even wondering that anymore.

It’s night-time conversations with God, saying, “I know You’re there. But frankly, I don’t have anything to say to You right now.”

It’s Heaven-flung violent, tear soaked pleas when your son stopped breathing and his oxygen levels dropped to 15/20% POST heart surgery – “God, please, SAVE MY SON!”

And it’s surrender and resignation all in the next breath, whispered – “God… please… save my son. But not my will, but yours be done.”

It’s feeling your heart break, a thousand million times, and not knowing if you will EVER feel whole or the same again.

If you yourself, will EVER recover from what you have seen and what you have walked.

It’s calling your husband as you walk down the corridors, saying, “I know I’ve walked these hallways 50 times already, and twice today alone, but I CAN’T REMEMBER. How do I get to the carpark? My mind is shattering under the load it’s carrying, AND I CAN’T REMEMBER HOW TO GET OUT OF THE HOSPITAL.”

It’s your toddler kicking and screaming in the hallways, yelling at you from the concrete floor, while you realise all the security cameras are watching you, and you look like one hell of an awful mother.

It’s watching your toddler struggle to handle knowing his mother is no longer there for him. It’s silent tears in the night, wishing you could be there to comfort both boys, while knowing you can’t.

It’s realising the impossibility of being there for two boys, who each now live in different suburbs. It’s trying so hard to split yourself in two, to be there for both, that you get sick yourself from the level of strain on you.

It’s looking forward to an afternoon alone of “special time” with your toddler at an indoor playground. Only to find your toddler completely disintegrates and screams at the top of his lungs, hitting his head repeatedly against a rubbish bin. It’s being asked by other mothers, “Do you need help?” And wanting to laugh insanely. But explaining calmly – instead – that you’ve been in hospital for weeks and your toddler is venting all of his fears and anger on you. It’s being let out the fire alarm door and setting off fire alarms because the owner of the establishment is so desperate to get you out of there, and your child is in no state to be carried back through all of the other parents and children.

It’s watching your baby vomit, and vomit, and vomit, and knowing you’ve got to take your screaming toddler to daycare so that you can rush your baby with bronchiolitis back to hospital. It’s watching while your toddler crushes your neck in a stranglehold, pleading and screaming with you, not to drop him off. While your baby waits in the daycare reception in a capsule on a monitor for his breathing and all the instructions you quickly gave were – “If the monitor alarms – call an ambulance.” And once again, it’s feeling your heart severed down the middle. Feeling utterly torn, that you simply can not be there for both boys. It’s handing your toddler over, watching him cry so hard he vomits too. It’s fleeing daycare, ready to utterly and absolutely shatter and cry yourself. And maybe vomit too, it suddenly feels appealing to join the crowd!

And finally, it’s packing yourself back up, mentally and emotionally. Piling all of the emotions, issues, struggles and fears into a little space, stuffing them all in, pushing them down, and straining to close the zip. So you can present… for one more day… that you can do this.

You think.

A Grandmother’s Sacrifice

The sun rises all too soon

Gran eases out of her cramped sofa position

Braces herself to meet another day

Ready to repeat it all again

.

She gently tucks Luke into his car seat

Together they begin the daily hospital drive

Scanning the cityscape for the Sky Tower
Monuments that mark this repetitive journey

.

This trip is all too frequent

As Gran pulls in to the hospital carpark

A small window of time

Reuniting Luke with his mummy and baby brother

.
Gran carefully juggles all his food and drink
And staggers through the hospital
Loaded down with bags of washing and a little boy
Ready for the cherished moments of connection

.

She gazes down at her smaller baby grandson

Hooked up to oxygen and heart rate monitors

A little boy, straining to beat the odds

A fighter with incredible spirit

.

Life held in fragile hands

He’s too young to know

That the fight in him

Comes from the grit in her

.

Luke bounds around the stark room

A bright vision of life and uncontained energy

Gran beckons him over onto her lap

As together they scan the sky for rescue helicopters

.

The moments gone too soon

Packed back up and loaded down

They pay the daily parking fee

And struggle to beat the rising rush hour traffic

.

Together they return home

Gran starts the usual

Preparing dinner, bath time, snuggles and stories

As Gran stands in for mummy

.

In the evening Gran shifts uncomfortably on the sofa

Waiting for when Luke will appear

Tearful and missing his mummy

.

With reassuring strokes she smoothes his hair

Kisses his brow

And returns him gently to bed

.

Her phone rings, time and again

Her own husband

Separated by land, sea and a plane ride

Holding the fort back at home

They check in around the day’s events

The latest medical updates

And think about when this season might end

.

A season of sacrifice

Separation

Away from her own husband and her own home

To sustain her daughter’s world

.

She settles back into her station on the sofa

One family still just held together

A journey still unfolding

Because of a grandmother’s unwavering presence

And a grandmother’s sacrifice.