Down the Rabbit Hole

Background info can be found RIGHT HERE

I want to preface this post by saying it’s taken me over week to put my thoughts into some semblance of order. And right now, I’m feeling too much at once, and I don’t know what to do with it. Because I’m pretty sure everyone is sick of me by now. So, I’ll retreat into my head, into the quiet… except its not really quiet. It’s full of every little thing I’m currently overthinking. So… to stop that, I’ll pick up the thread of the latest story I’m working on… this isn’t new. This isn’t… oh Stacey’s got her NICU records and is being dramatic again. Nope. I’ve done this my entire life. You just don’t see it. I made up stories. Wrote them down. Retreated into books long before that. Read Alice in Wonderland cover to cover far too many times and Oliver Twist. I still hate Wind in the Willows, But I still have that book. I’ve known since I was a teenager that writing was a coping mechanism. I just didn’t have all the pieces as to why it was a coping mechanism. 

Which is kinda where the NICU records come in. Sure they were totally to help understand where the cyst fit in. They really were. Because, that really hasn’t been fun to navigate over the past eighteen months. Only problem was, I wasn’t expecting everything else. I really wasn’t. The universe sure does have a twisted sense of timing though. That… or maybe there really is someone looking out for me. It’s too early in the emotional jet lag to say thank you. I still want to rage. I’m not doing crying and I want to really really want to kick something… or someone.

I still don’t get how I survived it. I mean, I do. Medical intervention is a hell of a thing. But a Grade 4 IVH? Come on… I don’t get it. How!?

I can’t remember if luck was ever thrown around when I was younger. God, I know I used to throw it around with my daughter. No brain bleed in her case. She got steroids (I didn’t). She still got ROP though, I think. And she wasn’t a menace like I was. Or was it trouble. Either way. “Her brain is fine.” Noel’s words not mine. 

It’s strange how the past finds you just when you’re trying to make sense of the present.

I knew it was bad. I heard how I was “special” growing up. How the doctor’s didn’t know why I came early. Lie. My mum had a bleed one week prior to me being born. She probably had a placental abruption and started contracting and they couldn’t stop the contractions, much like my daughter. Redacted file. The doctors knew. I’m sure of it. There’s always a reason.

I don’t get why it’s such a shock honestly. I mean, a part of me does. Because, I’m not sure I should be here and I don’t know how to reconcile that with the fact that I am here.

Because I didn’t just survive a Grade 4 brain bleed. I survived sepsis, a bilateral pneumothorax, anaemia, seizures, PDA, blood transfusions, dehydration, metabolic acidosis, HMD (or RDS), and Grade 1 ROP. I survived.

But then I got to the part where some of my child development reports were included, and the past caught up with me in double time. The doctors seemed to rule out cerebral palsy for a while, but the fact I have “mild cerebral palsy” now must mean they settled on it. I don’t know what tipped the scales in the end. At one point I was about 12 months behind in my development. My mother never let go of the possibility of me contracting AIDS, from the blood transfusions I had to have despite reassurance from the doctors, nor the fact that the doctors noted borderline retardation. I think she died thinking I was stupid, and I both resent and hate her for that. I’ve carried that my entire life. I’ve hid from that my entire life. Is it any surprise I turned to writing and stories and prefer to get lost in the worlds and people I made up in my head? It was hurtful enough being called pathetic and stupid growing up when she was drunk. I could almost excuse it. But I’ve learnt a far bit since she died, and you know what, maybe I don’t forgive her, and maybe I’m okay with that. Or at least I will be eventually. What’s that saying? Information is power?

I think that’s what’s hit me the most: seeing her “concerns” on paper, seeing the doctors write that despite the odds, it could have been worse. I survived. My brain rewired itself. I guess that’s one way to put it. Sitting here, looking back over everything. Going down a massive rabbit hole, the pieces are starting to fit. It’s ticking boxes I honestly didn’t see before. All my life I’ve always been able to explain away my personality as a premmie thing or a CP thing. I knew I was weird and awkward and shy. I was bullied because of my disability. My grades suffered because I was premature. Because of developmental delays etc. But what if it’s not just that? There’s other things. Stuff that doesn’t always get picked up. Things like walking into work and not verbally saying anything. In my own defense it’s a busy call center and I didn’t want to interrupt but in proper social circles that’s actually rude. Yeah um… oops. Don’t worry, I greeted everyone in chat. (lol) Maybe that’s why my granddad always greeted me whenever I walked into his house, without expecting me to say anything first. But if it’s not the social norm… then maybe what I’m dealing with is autism and adhd and because it was the 80s and I was so very very prem and so sick and a girl it all got missed.

So… that’s where I’m at. The rabbit role kinda stops and loops back on itself from here and its maddening. I don’t know how to get comfortable with it. Any of it. Not my disability. How do you stop running from who you are when it’s all you’ve done your entire life? No answers. Only puzzle pieces that are starting to fit, but still leave me feeling like I’m just the quirky girl who’d rather be reading or losing herself in stories of her own making and gets mad when she can’t. Deep down I’m still me. I believe that. But my ability to overthink and hyperfixate and just straight up dwell are going to be at war with with for a while. I can feel it. I need an adultier adult. Somebody send help, because, I’m going to need it… and if you think you’re sick of me now… haha… please don’t unfollow me.

And as for all things migraines… the neurologist doesn’t think the migraines are epilepsy or seizure-related. Which might be a relief if the meds I was prescribed would actually work. Since I’ve been tracking my migraines by way of an app, I’ve had a persistent migraine for over four days. I tried to tell the neurologist they don’t go away, that they are with me pretty much constantly. I guess this will show him. It’s hard to be upbeat when the week ends on a pain spike. Which is ironically where it started.

Was I hoping for some kind of magic wand? No? But I was hoping for meds that would give me a bit more relief. Yes. The combined effect of Panadol, Topamax, Propranolol, and Imigran have managed to either make the pain worse or keep it at it’s current levels. And all I want is for it to stop completely. 

Tales Of Magic, Mischief & Mayhem

At ten years old, Morgan’s life was shattered when Uther Pendragon murdered her father. Years later, with the Morrighan—a goddess of war and fate—at her side, Morgan finally claims her vengeance.

But her victory comes at a cost: a vision of Arthur’s untimely death and the fall of Camelot.

Can Morgan defy the Morrighan’s prophecy to save her brother and the kingdom, or is Camelot doomed to crumble under the weight of destiny?

A tale of revenge, power, and sacrifice. Step into Morgan’s world and uncover the magic behind the legend.

 

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A Love That Defies Time…

In the shadow of rebellion, Angharad, daughter of Owain Glyndŵr, is captured by the English and imprisoned in the Tower of London. Her spirit remains unbroken—until a mysterious power sends her and her captor, Gareth, through time. Transported into Gareth’s future, Angharad faces a world she never expected—and a love that bridges centuries.

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Discover the Magic of Wintertide + Fey-Inspired Tales

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A Love That Defies Time…

In the shadow of rebellion, Angharad, daughter of Owain Glyndŵr, is captured by the English and imprisoned in the Tower of London. Her spirit remains unbroken—until a mysterious power sends her and her captor, Gareth, through time. Transported into Gareth’s future, Angharad faces a world she never expected—and a love that bridges centuries.

This Christmas, Wintertide brings you a tale of defiance, destiny, and a love that cannot be denied. Will Angharad embrace a future with Gareth, or will her past pull her away? The ultimate Christmas gift could be a promise of forever.

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What are you waiting for? Check it out now!

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Looking for your next read? Dive into a perfectly curated collection of romantic fantasy and sci-fi books! Whether you’re captivated by magical realms or futuristic adventures, these stories will sweep you off your feet. From love that defies time to forbidden connections in distant galaxies, there’s a romance waiting for every reader.

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Gravity

flat1000x1000075f-u12Background info can be found RIGHT HERE

Ha! We’re not done yet. Not even close. I’m not going to rehash what’s happened in the almost 6 months since I last commented on the hell that is this shit show. It’s fucked… 100% fucked. I don’t even have enough curse words, I’m so angry.

Okay, the anger hasn’t really gone away. It simmers, sits in the not so distant recesses of my mind and just stews. Not very helpful or productive… or anything much really. It just is.

The second MRI was a joke. Stable appearance… fuck off.

If it hasn’t grown… ha spelling almost got me… yeah that’s my reality now.

I’ve lost the remaining vision in my left eye… so that’s fun. Couldn’t tell for a few months, because of the mind altering pain, and because when you can’t see well out of one eye you kinda get used to a certain degree of blindness, but then May 16th happened and the vision died and then my brain was trying to make sense of the loss and light was behaving weirdly and I had to move my head to cross the damn road, which felt strange, but all the pieces took time to actually fit together and cement that my vision in my left eye has changed. So, that was determined in July.

So… vision loss… left side migraine like headaches that don’t respond to meds. Latest med to fail… propranolol. Somehow the pain spikes when I take it, settles a fraction and then I live at a 4-5. I think. Pain scales have no meaning anymore. I don’t know where I am because this has been my constant for the last 6 months… longer actually cause it’s December. Another week and we’ll be in 7 months territory.

I don’t want to. I’m beyond done. If I could curl up into a ball and just shut the world out I would.

How do you advocate for yourself when even your GP throws up his hands and denies you a second public health referral on the grounds they’d ask too many questions. WTF!?

So, now I’m counting down the mandatory wait times for a pre existing condition on private health and I hate that too.

And if the cyst hasn’t grown… he’s a random thought… fuck here’s… if the cyst is 36x21mm was it always that big? And if so… how much room did it take up in my tiny 830g 27 week premmie brain?

I’m obsessing, but these are the thoughts that actually don’t keep me up at night, but do creep in.

I shouldn’t be here. I’m lucky to be alive, I get that.

But this… this… if I go to a private neurologist and I’m given the diagnosis of some form of migraines I may scream the fucking place down… migraines don’t cause vision loss. I refuse to believe that I am a rare enough case that I’m like the 1% or whatever that actually lost my vision to fucked up migraines.

Migraines can/do cause neurological damage over time… I think. I’m clutching at straws… I really don’t think its migraines.

It’s hard to focus on getting answers when you’re battling the constant fear that you now have an expiry date. Yeah, I said it… I went there. Fear can be a powerful motivator… totally. Except in this case, all its doing is making me aware of every little thing I have done.

Anxiety sucks.

Depression is hell.

And if I had the ability to just drown in both… I would. Except I don’t because of the 101 other things I have to do.

So, now I just need to find a way forward, while the medical feild just fobs me off.

And maybe attempt another new medication in the meantime.

 

Nothing Left

wp5780488Background info can be found RIGHT HERE

It’s been seven days since my last post. God… I sound like a cliche.

Waiting on a neurosurgery appointment sucks. The public health system is horrible. It’s broken.

And my only recourse it seems is more waiting… 6 weeks since the ED… then 18 days of pushing for a damn MRI and then another 18 days since I discovered this cyst. Weirdly, it’s not the cyst that bothers me so much, it’s not knowing if the damn thing has changed or shifted in 40 years. It’s having constant headaches… because they don’t leave, they just sort of sit underneath the surface ignored until they peak. It’s the side effects of naprozen and tramadol.

It’s the numbness and tingling, its freezing in stressful situations and not being able to articulate at work what’s going on because I have to concentrate harder to process all the information and then regurgitate the information as I’ve gotten it.

And then there’s the compartmentalizing. I’m still floored by the fact that my GP told me to compartmentalize this latest bout of acute anxiety. Her words, not mine. As if I can put a band-aid over the worry and concern. Over the fear of the unknown. I’m not dying, but as an adult shoving shit into tiny boxes and ignoring it isn’t helpful.

I swear nobody wants to take me seriously. The: oh this could still be atypical migraines. Like is there something the GP is not telling me? Why would I make up not knowing about a cyst that I have likely had since birth?

Why would I want to revisit being born at 27 weeks if I didn’t have to? If it wasn’t medically necessary to separate what is normal to what is not normal? But that’s okay, let’s ignore the numbness and tingling shall we? No, because while my left side might have been weak, there was no numbness or tingling.

And I certainly wasn’t as aware of the loss of vision in my left eye as I am right now, and that scares me a little. But, I’ve never seen very well out of it to begin with so it’s hard to say with certainty if there is a change, which is annoying to say the least.

So, what do I do, while life keeps moving on around me… Iron Faerie… God, why did I think it was a good idea to try and continue that endeavour? Oh, wait… because it wasn’t hard nor stressful until it got hard and stressful.

I don’t get the medical profession honestly. You wouldn’t make someone with a broken leg try so hard to get medical attention. Why am I having to fight so hard. What lesson is there in it? I’m bloody tired of fighting. I’m tired of being strong. But I think I’ve said this before. Even so, it’s still true.

Until the next time, my anxiety or depression get the better of me. Pray they don’t. Because I’m not sure how much more of this I can take honestly.

Barely Breathing

 

 

 

 

Background info can be found RIGHT HERE

If you know the song… kudos. If you know me in real life… even better. Learning the hard way lately that I don’t breathe enough in all the things.

Which is ironic because of how I came into the world. Early and in a rush… apparently.

I’ve been sitting the last few days having no choice but to reflect on everything. Because everything is tied up in a messy little bow… everything is linked and I still hate it. All the hate.

All the anger.

It hit me yesterday, that’s what all of this is. It’s anger at everything and everyone. It’s all the feelings that the teenage me was able to say: STOP to… but the adult me for whatever reason… can’t.

So, was I better at dealing with shit then than I am now, or was I just so overwhelmed with life that it just became normal?

So much in my childhood wasn’t normal, but that was life and we just got on with it. And weirdly that’s not what bothers me… okay maybe a little because I’m overwhelmed by everything that happened to land me here, and I’m revisiting stuff and when a large part of it is tied to the one person whose been dead for coming up sixteen years what else is there but anger?

I can’t talk to her. I can move on from my feelings surrounding the way she dealt with it. I mean I can but at the moment, how the fuck do I get closure from a dead person. She didn’t let go. And that’s okay I guess, but now in order to deal and cope, I’m having to breathe and maybe I just don’t want to and that’s sorta scary.

So if all of this now is past trauma and grief and fear of the unknown and all the dark and twisty bullshit that I usually reserve for characters in the books I write… how the hell do I unravel it? Can I even?

I’d always viewed it as a kid as beyond my control. I was born 12 weeks early… didn’t find out it was even 13 weeks early until my daughter was born in 2007… didn’t even consider the genetic link until sometime in 2009. But it’s there.

And it still is. But… I’m symptomatic. I’ve found recently I hate taking pills. The lower back pain and the hip dysplasia and the bursitis… it’s weirdly taken a backseat. Even though I should be dealing with physio because surgery is needed on the hip. But the rock keeps moving. Life keeps moving.

And that’s the problem. Everything is moving and I need time to catch up and I can’t. I don’t have time.

So, how do I fix the mind numbing wait for neuro and the silence? Well psych suggested keeping busy, which I’ve caught onto already. But sleep is much more enticing. So is alcohol but I’m quite deliberately staying away from that. Thanks Mum.

So, it’s music and blogging and binging TV and existing but not existing at the same time… it’s the quiet that gets me… those moments between calls at work… I’ve noticed a shift in things there. Funny how all this is having a flow on effect at work, because the customer service voice I’ve adopted is usually really upbeat and perky.

Guess the masks are coming off… not sure how I feel about that.

I don’t like this level of vulnerability. It’s almost too much in and of itself.

Usually when life craps out it’s because of things others are doing.

This… coming from within… living with it… trying to deal is just hard. It’s icky and I hate the anger but it appears I skipped over denial and went straight to the second stage… oh wait… no I did have a moment of denial… in the wait and frustration leading up to being told about the damned cyst.

I wished it was just a migraine. Yep. Awesome.

So… over it, and I’m not even past it.

Thanks universe. You can fuck off now.

This is not how I wanted to come back, but…

I hate this.

The universe keeps wanting to kick me… or maybe I’m just not getting it. Maybe I’m meant to advocate for this shit. I don’t know. I don’t really want to, because that’s not me. Or it wasn’t. *shrugs*

There’s no light at the end of this tunnel. I remember at sixteen, seventeen years old being incredibly angry at my mum… for so many things. Mostly her inability to let go.

Being born at 27 weeks and weighing 830g at birth in 1983 comes with its own challenges.

I coped, sort of. You get to a certain point where you can walk and do all the things and you’re just done. You’re normal, or so you think.

Nope. Universe shitting on me again.

16th May 2024.

3pm or near enough. I’m not a numbers person, but I’m starting to think 3 might have some significance because it was 3:45 when I had to dash out of a previous job bleeding at 28 weeks and 1 day pregnant… that was scary.

This was that but different.

It started with my left eye, I’d been having constant headaches on the left side since May 1, worked through them, until the 15th May where I thought… maybe a dr’s visit would be worthwhile, because it can’t be right. But I had just gotten through a rent inspection and changes at work and medication for hip and back pain… maybe, just maybe it’s a headache because of the meds. So I stopped those completely May 3rd and just lived through back and hip pain for a while. Which thankfully wasn’t as bad as it could have been.

Anyway, it started, and it progressed to my lips being tingly and the left side of my face being numb, but when I was getting pins and needles in my left hand… that’s when I started to think, this isn’t a migraine. I can’t see at all well out of my left eye, so I can ignore things to a degree.

Cue panicking my team leader… probably a good thing I was in the office, I was, just like all those years ago in 2007, considering working through… 2 hours left of my shift… was also considering walking the few blocks to the emergency department, as you do.

Instead what happened was an uber, followed by a seven hour wait. The ED is actually quite fun when it comes to people watching. If I’d been there with my kids for any number of things we’d been there for in the past, maybe I would have engaged more.

But when your symptoms match that of a stroke it’s not as easy.

So I had my phone… no book… god never go to the ED without a book… and I had several people trying to keep me distracted through messages. I made some calls and just generally waited.

Finally, at 9 (yes I manifested that one… next time I’ll go for a less then 7 hour wait) I got in with the nurse, a lovely guy with an Irish accent.

And this is where advocating for myself went wrong… I have cerebral palsy with left side weakness. I have migraines. None of this was new, but as my husband said today, it’s changed.

Except unlike my husband, the ED weren’t listening to the fact things had changed.

When you watch your left side not react because its numb and the reflex responses are fucked up… yeah I was silently freaking. I may have voiced it or maybe I thought it. That’s not normal.

Diagnosis by neuro was to get a CT, give IV pain meds, not Tramadol because maybe it could be that, but it shouldn’t be a medication overdose headache, but we’re leaning towards an atypical migraine at this stage. Also I should note that the pain scale and I are not friends. I figured out after the fact, that my: I’m still having pain but it’s a 1-2 was in reality a 4-5 on the pain scale.

At 1am I had a CT… at this point after shivering all the way through the CT I was offered a blanket. They were so busy, I was never told where the call button was or asked if I could have a blanket and because they’d ruled out anything serious, I was ignored. Maybe I should have been more vocal, but it was really late.

On waking my pain was almost non existant, and my CT was clear, despite certain white matter loss and my 27 weeker status.

The “Oh you’d never know you had cerebral palsy or were prem” got old… fast.

Something wasn’t right. I knew it. But I had discharge orders and follow up with GP for an MRI.

Okay. Fine.

Side note: I hate hospitals. I’m not a great patient. I get restless and bored easily and feel trapped. Maybe it’s a prem thing. Maybe it goes back to being little and having surgery to lengthen my left tendon and being alone and wanting my parents, but they had to work, care for my sister etc and couldn’t be there… I don’t know.

So I left, had my dad take me home, and then after doing all the things I needed to for work… slept. Because at this point the headache was back.

Now here is where it starts to go downhill.

I worked Saturday.

Saw the GP on Tuesday, who told me: At your age and low risk it couldn’t have been a stroke, it’s got to be migraines. Get the bloods and we’ll see what’s what.

At this point, it’s really starting to sink in that it’s not a migraine. No migraine I’ve had in my life has ever presented with these symptoms.

Spent a week trying to get bloods. Long story. Inexperienced technician trying to tell me I was dehydrated. Fun times.

Go back to the dr for the results and to push for an MRI… oh that will be $400 on you because I cannot bulk bill. Only the ED can. I will follow up.

On the 29th I get the blood test results… nothing wrong except really low iron levels. Discuss options and then bring up the fact I’m still having headaches daily and the numbness, tingling has not gone away. So the GP rings ED and presses them for an MRI. She’ll get back to me with answers on that. Okay, but if it’s a no I’m paying the $400-$500 out of pocket. (Yes the figure rose, while she was talking to the ED)

Fast forward to June 4th and I’m back at the doctors because I’m still having symptoms after freaking myself out at the end of May… love jumping at shadows… not.

So he.. yes I switched drs because the GP I’d been seeing for the headaches, is now on holidays. No she didn’t think it was important I know that she was even going on holidays.

I tell him my story, he does all the things… including: Oh we can totally bulk bill that MRI for you, we just need to write all the right things on it.

SERIOUSLY!!!! So angry at this point. WTF!?

Now here’s the fun part. I ring SKG not expecting to get an appointment the same day. I did, yay for cancellations. Side note: if it hadn’t been bulked billed which it was it would have been $275… heaps cheaper than the $400-$500 from earlier.

So I get the MRI… left with a headache.

Then there’s an agonising wait for results with yet another GP because I wasn’t waiting any longer than I had too.

Monday 10th June..

More fun. GP: You know you’ve got a cyst right?

NO!

Cue me in a completely panicked fashion explaining what I know of my own medical history. The prematurity. The stroke I had as a baby, the almost dying, the 10% chance of survival… on and on. I don’t remember having any brain scans as a kid. Maybe I should get my NICU records.

GP: Yeah that might be ideal.

FUCK.

Walk home. Yes, I walked. Finally got a script for migraine meds. Don’t drive on them. Yeah I don’t drive, so not a problem there. It was probably the longest 15 minutes of my life. Hubby went as far as to say he would have come with me, but me for many reasons just wanted to get it over with and went to the drs alone.

So… its a cyst. A porencephalic cyst to be exact. I’ve had it since I was a baby. The symptoms are common. The deficits align. I haven’t unpacked that yet.

Everything fits. I had a stroke and the cyst formed because of it and the cerebral palsy… all of it is likely because of the cyst. But most kids have it removed/dealt with as a child. For whatever reason… be it medicine or just that it didn’t show on those initial NICU scan it was missed.

It’s been a week since the referral has been doing its thing. I haven’t got word that it’s been accepted yet, and it could be rejected.

I’m currently living with a porencephalic cyst in my head that has changed in someway. It’s 36mm x 21mm… it doesn’t seem small to me.

Frank… hubby named it… is hell. I’ve got a massive amount of what ifs coursing through my mind and no answers. It’s sucks. Did I mention how rare it is? 3.5 live births in 100,000.

That’s… 0.0035% of the population.

But I’m working through.

I took a day off recently because I spiralled and couldn’t make it out the door to actually go to work. Weirdest feeling. Worse was the: aww, I wanted to see work peeps.

The introvert in me isn’t normally like that.

So what am I dealing with you might ask? Besides Frank…

Well…

Left side tingling and numbness. This can be anything from my left eye feels tingly to walking around on a numb left leg. Fingers/arm with pins and needles. Numb left side of my face. Rarer is the left side of my head is numb.

Headache. Left side. Regularly sits at about a 4-5. It has peaked at a 9. It was late. I almost called an ambulance, but all I wanted was sleep. So I just burst into tears instead.

Migraine meds (the cocktail of Naproxen, Tramadol and Rizatriptan [makes me nauseated] bring it to a 1-2) Zero pain is rare. I want zero. Probably won’t get it.

Vertigo. If you’ve ever been dizzy, vertigo is another level. I was sitting – talking – and the room spun around me.

Nausea… though likely the meds I take.

Trouble processing written information. Trouble spelling. Trouble multitasking. My reaction times are slower. It’s going to seem like I’m making these up. Because I’ve had some of these deficits prior to May 1st. But… these have all changed. Spelling is masked mostly through me self editing before or after I post something… or autocorrect. Word finding difficulties. Had a moment at work… scared the crap out of me. I couldn’t talk. The brain was trying to compensate and I just couldn’t speak. I had a moment where I couldn’t remember my sons name. I was looking at him, while my husband was talking about our eldest son…. and I just couldn’t grasp his name.

I think collectively the above fits with aphasia, but god knows.

None of this is regular… except maybe all the cognitive shit. It’s hard to tell. The anxiety which I live with, but what I had handled because work is a huge distraction, is kicking my arse. Depression is too.

Ironically, this is the most I’ve written in weeks… it’s not even escapism. Which honestly, I want write now. (the spelling error is deliberate because this is what I’m now dealing with… I thought “right” but my hands wrote “write”)

I’m craving things I shouldn’t… I can relate to people I never wanted to relate to in a million years.

I miss my mum. I actually find myself wishing she hadn’t been stuck in her own patterns and coping mechanisms because maybe instead of being scared and anxious she would have been able to fight.

I’ve always said seeing the NICU from the other side is a whole other level. I lived it. I was in it. And then I got to go back at 24 and experience it first hand. Have a conversation with Dr Noel French (my paediatrician who wasn’t my daughters paed) about my daughter’s brain. Meet some of the nurses looking after her that looked after me.

Leaving that hospital without her… was hell.

I don’t want to be back here. Reliving childhood crap. Dealing with all the feelings. It’s impossible to deal with all the feelings.

I want out. I’m done. I’m 40 years old, dealing with a neonate insult.

I don’t want to.

And the rational part of me goes. It’s not cancer. It’s not much of anything. It’s a cyst. I’ve had it my entire life.

But this is the thing. There are changes. And fuck… I’m a writer. It’s in my soul. Has been since 1997. I’m published. Freaking USA TODAY Bestselling Author tag. Doesn’t get better than that. So the changes to my cognition… scares the absolute crap out of me. Because I have a shit tonne of unfinished stuff. And Iron Faerie won’t run itself and all the things.

I want Frank out, but that’s brain surgery and um… I’m mentally running the other way and facing my own mortaility… because anxiety… and worse case scenarios.

Heart, Lungs, Brain… that’s the issues premmies cop. I come across that yesterday I think with a advancement posted by 9News 8 years ago… that said drs in Perth had found a way to test blood in pregnant women to see if they had the gene for prematurity.

Dr Alfred Asher Grauaug was the prioneer of the NICU of King Edward Memorial. He was my doctor. Dr Noel French is retired but I know I was part of his research in the 80s and 90s. And I appeared before a bunch of scared NICU parents during my daugher’s eight week stint because I was in his words: one of the success stories.

I survived.

But now I have a cyst and it sucks.

I’m not suicidal. I don’t know what that looks like.

It’s never been an option.

But shit is hard and I don’t struggle well, and asking for help. Fuck that. I can fake that I’m okay right?

Maybe not. Cause I know I’m not okay, but voicing that is hard.

Where did I leave that mask?

Tips for Surviving NaNoWriMo

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Yes. It’s October and you know what that means. NaNoWriMo is coming.

It’s October 15th which means there’s just over two weeks until November is upon us.

Eek! Don’t ask me what I’m writing cause I don’t know yet.

Having participated in NaNoWriMo (National Novel Writing Month) since 2005, I like to think I’ve picked up a tip or two along the way.

So, I’ve decided to share.

Tip #1: Pace yourself. Writing 50,000 words in 30 days may seem like a massive undertaking and leave you feeling completely overwhelmed, but the truth is it doesn’t have to. 1,667 words per day is completely doable, and if you break it down into even smaller goals… say 834 words in the morning and 834 words at night it’ll be an even easier goal to smash.

Tip #2: It’s never to early to kill off a character. In NaNoWriMo… anything goes. I once killed of a main character in the first chapter. Surprisingly, it worked and pushed the other characters forward. Death scenes take up a lot of words. So, does sex.

Tip #3: Editing is for December. Turn off your inner editor. Yes, it’s hard, but completely doable.

Tip #4: Turn off distractions. Procrastinating is the worst enemy to any NaNoer. If it helps set a timer, and turn off the WiFi. Research is fun, but time consuming.

Tip #5: Have fun. Because if you’re not having fun while writing, there’s really no point.

And there it is. I hope you find these tips helpful.

Motivation Monday

 

New Monday = New Week!

Monday’s are for fresh starts! Who is with me?

Not to mention all the new goals and new plans waiting to be unveiled.

So, what did you accomplish? Good things I hope.

Currently, I have Pendragon awaiting further edits, A Rueful Equinox sitting at just over 2700 words and… A Curse of Thorns & Roses is in the planning stages. And that’s just my writing projects. I’ve also been editing short stories, creating various content which I hope to share with you soon. As for my little Monday ritual it usually involves coffee and cake.

I’ll be sharing future progress and if you happen to have made any of your own, please do share in the comments… no matter how big or small it was!

And don’t worry if you didn’t make much progress today is a new day and the start of a new week.

Just work the steps from this post and you’ll be on your way!

Motivation Monday

 

New Monday = New Week!

Monday’s are for fresh starts! Who is with me?

Not to mention all the new goals and new plans waiting to be unveiled.

So, what did you accomplish? Good things I hope.

I did a lot this past week and I’ve got a lot of balls up in the air to get on with over the next week.

We’ll see how productive I am next week.

What’s your Monday ritual? Did you make one? 

I did!

What about you?

I’ll be sharing my ritual along with weekly progress reports in subsequent Monday blog posts.

Share the progress you made in the comments no matter how big or small it was!

And don’t worry if you didn’t make much progress today is a new day and the start of a new week.

Just work the steps from this post and you’ll be on your way!

Motivation Monday

 

New Monday = New Week!

Monday’s are for fresh starts! Who is with me?

Not to mention all the new goals and new plans waiting to be unveiled.

So, what did you accomplish last week?

Did you make your Friday more productive? Or did you struggle with it like I did?

What’s your Monday ritual? Did you make one? 

Did you set a weekend routine? If spending both days writing counts, I totally nailed it.

As for Monday’s not sucking… well I’m still working on that. 

How about you?

Share the progress you made in the comments no matter how big or small it was!

And don’t worry if you didn’t make much progress today is a new day and the start of a new week.

Just work the steps from last week’s post and you’ll be on your way!

5 Questions to Ask Before Starting Your Novel

Have you ever found yourself stumbling over where to start on a new novel? I have.

So, below I’ve come up with five questions to ask yourself before you get started writing.

They are:

1. Who is the main character or the heart of the story?

2. Who is the antagonist?

3. What threatens your main character?

4. What is the catalyst that sets the story in motion?

5. Where does the story end?

If you’ve answered all five of these you should have at least some idea as to the direction your story is headed.

I hope you found this blog post helpful in some way. If you did, drop me a like or a comment below.

Throwback Thursday

 

To be honest, I wasn’t sure what to post today, so I thought I’d re share one of my older posts that seemed to resonate with readers the first time around in 2018 when I posted it in May. It’s called What Makes Paranormal Romance, Paranormal?

Maybe you’ve read it and maybe you haven’t.

It’s short and doesn’t quite go into all that much depth, but it’s going to kick off next Thursday’s blog post, and I needed a reminder as to why I love writing today, because one of my WIPs is being oddly difficult.

And who knows… maybe it’s spark something within you guys as well.

Fingers crossed.

Motivation Monday

New Monday = New Week!

Monday’s are for fresh starts! Who is with me?

Not to mention all the new goals and new plans waiting to be unveiled.

I’m not the biggest fan of Monday’s to be honest but I’m looking to change that. And I thought what better way than to bring you guys along for the ride with me and maybe see some positive changes in your lives as well.

So, how can you fall in love with Monday’s?

1. Make Friday Productive.

Have a slower start to the working week by preparing the best you can on Friday. Put in a lot of work on Friday. So you don’t have that much on your to do list for the new week. Get the most difficult tasks done on Friday so that Monday doesn’t have to be crazy and full of stress.

2. Create a Monday Ritual.

To start loving Mondays find a habit, a treat, or a ritual – something that you really love and look forward to and make it happen.

3. Stop derailing yourself on the weekends.

Most of us love to sleep in on the weekends but it isn’t always practical. You’ll find yourself getting exhausted fast. To avoid that keep your weekend sleep schedule similar to your weekday schedule and you’ll soon find yourself ready to take on Monday.

4. Change your mindset.

Stop telling yourself that Monday’s suck. The truth is they don’t. It’s just that for some of us the weekend never lasts long enough. Instead think of Monday’s as a fresh start. A new chance to go after things that matter most to you.

I hope this gives you a much needed boost to take back Monday and mould it into something you can learn to love.

The #1 Thing That Will Make a Difference to Your Writing

Want to know the one thing that will make a difference to your writing?

Well I’m about to share it.

Get ready.

It’s reading.

Yes. READING.

Now, I know what you’re thinking. It can’t be that simple, right? Wrong! It really is that simple.

Immersing yourself in the genre you’re writing in not only helps you with language and style but also with finding your writing voice and it also helps with grammar and spelling. Something every writer at any stage can benefit from.

I don’t know about you but my grammar is often weak, especially in my longer works. But I’m working to improve it, and reading helps me to recall certain grammar rules.

It also helps your mood by helping you relax and centre yourself. Plus if you’re anything like me, reading a paperback book can aid in helping you fall asleep.

So, what are you waiting for? Go on and grab yourself your next favourite read and get cracking.

Paperback books are still my most favourite thing to pick up and read, but kindle is a close second.

What’s your favourite? Paperback or eBook?

Comment below!

Bonus points if you share the title of the last book you picked up and read or are reading!