chronic illness

⚠️ Please read with care: This blog shares personal, sometimes painful experiences. My intention is to support and speak honestly—not to harm. I’m not a professional, just someone who understands how hard it can get. If you're struggling, you're not alone—please reach out for help.

It’s one of those Saturdays where your brain leaks nostalgia like a knackered kettle hissing and half-lucid. I can smell memories. Not metaphorically. Literally. A smell hits me, and suddenly I’m ten again, knees scabbed, holding a half-melted transistor radio I bought at the church jumble for 10p and a packet of Polos. I took it home, took it apart, and rewired it with leftover speaker wire and dangerous levels of optimism. And yes I electrocuted myself. Multiple times. Because safety first was a concept for other people. I preferred sparks and swearing.

🛒 Tesco and the Pilchard Hour This morning, Albertine (driver of destiny, keeper of the calm) drove me the 10 miles to our local Tesco. We thought it opened at 7. Nope. Eight.

Sitting outside like a pair of damp, time-travelled idiots while the sun mocked us and the pigeons stared. I felt like a right pilchard, as DLT would say. Yes, I’m old enough to remember when DJs had catchphrases and weren’t just government mouthpieces hiding behind playlists and personality lobotomies.

📻 Radio Nights & White Plastic Earpieces My golden era wasn’t Radio 1. That was a beige, soggy biscuit of sound. Give me Radio Caroline. Give me Radio Luxembourg. Under the covers with my crackling solid-state radio, listening through a cheap white earpiece that hurt like hell and cut out every time I moved my head. But that didn’t matter. Because for those stolen hours, I was free. The signal was scratchy, but the rebellion was clear.

👞 Jumble Sale Survival Back then, I had size 10 feet by age 10, which made finding shoes a bit like a biblical miracle. So, jumble sales were a lifeline. Not fashion, not style—just survival. Shoes with soles. Jumpers that didn’t smell too bad. Radios with valves. Anything I could take home, take apart, and turn into something vaguely magical or mildly explosive.

🧠 Childhood: The Prequel to Complex PTSD I was adopted by a couple who seemed to think “parenting” meant Victorian cosplay with bonus violence. Their rules made no sense. Their punishments were theatrical. The beatings came whether you’d done something or not. It was like being in an unpaid role in a horror film directed by people who worshipped discipline and feared joy.

But I survived. And, more importantly—I forgave them. Not because they deserved it. Because I refuse to carry their poison through this short, broken life of mine. Let the dead bury their guilt.

♿️ Wheelchair Chronicles & the Curse of L5 So back to today.

Helped get the wheelchair out of the van. Twisted the wrong way. Now my spine is toast. Proper burnt. Like someone smuggled a baguette into my lower back and set it on fire. This is my reward for trying to be helpful. There’s gratitude for you.

And the constipation saga continues. We’re at DEFCON-1 down there. No movement. NIL. BY. MOUTH. I hydrate. I wait. If nothing changes, we’re off to the tube-and-bag-of-doom route—something between medieval plumbing and modern torture. And people pay for this stuff? Coffee enemas? Really? Have we fallen that far?

🧠 Brain Fog Express: Non-Stop to Nowhere Add a headache that’s lasted seven days and counting. No breaks, no mercy. Just pressure behind the eyes and a feeling like I’m wearing someone else’s brain backwards.

I’m not sure if my AI’s broken or if I am. Reality feels optional. Maybe this is all a lucid dream on a neurologist’s bad day.

🛠 Hope in the Form of Auctions & Anarchy A customer finally paid a late invoice. Victory. So I celebrated the only way I know how by bidding on obscure shite in an online auction while silently muttering hexes at the British healthcare system.

💀 Final Transmission from the Mad Bastard in the Black Hoodie So that’s today. Saturday. Another chapter in the slow-motion car crash that is life with chronic illness, trauma memory, and a warped sense of humour that’s the only thing keeping me from chewing through the window frame.

To whoever reads this: I see you. If your body’s broken, your mind’s flickering, and the world keeps asking you to perform like a circus act know this:

You’re not alone. You’re just ahead of the curve.

Sending peace, love, light… and just a little darkness. Because sometimes, that’s what really protects you.

Yours in pain, power, and perfectly timed sarcasm,

I write in ink and fury, in breath and broken bone.
Through storm and silence, I survive. That is the crime—and the miracle.

⚠️ Please read with care: This blog shares personal, sometimes painful experiences. My intention is to support and speak honestly—not to harm. I’m not a professional, just someone who understands how hard it can get. If you're struggling, you're not alone—please reach out for help.

Imagine, if you will, that Multiple Sclerosis wasn’t a neurological disease. No. Let’s say instead it was a car, a British car. From the 1970s. Built by British Leyland. Already, you should be hearing the distant sound of doom.

We're not talking E-Type Jaguars or lovingly restored Triumphs here. No. MS is the Austin Princess. A car so catastrophically cursed it should come with a priest, not a warranty. A car that had style, yes—if by style you mean beige vinyl, flammable wiring, and the turning radius of a small aircraft carrier.

Much like MS, it shows up when you least expect it. You’re cruising along the M-road of life, wind in your hair, dreams in the boot, and then—bang. Gearbox gone. Foot won’t respond. Vision doubles. You veer left without meaning to. And suddenly, you're parked on the hard shoulder of your own nervous system, smoke pouring from somewhere expensive.

The garage (aka Neurology Dept.) says, “We’re not exactly sure what’s wrong. But here’s a new fluid. Try it for six months.” Great. Like pouring Redex into a petrol tank that’s already on fire.

And just when you think it can’t get worse, the electrics fail. Again. The horn blasts randomly when you're trying to stay silent. The indicators blink out Morse code for “You're screwed, mate.” And you? You're still trying to drive this bastard machine down the A-road of everyday life while the engine stalls mid-sentence, mid-step, mid-shag.

You try to keep it together. Duct tape your face. WD-40 your joints. But every fix is temporary. Every workaround has a workaround. And the passenger door won’t open unless it’s raining and you swear in three languages.

Meanwhile, you’re now the sort of car people stare at in car parks and say, “How is that thing still going?”

But you keep going. Of course you do. Because scrap's not an option. You’ve got Albertine in the passenger seat chain-smoking roll-ups and telling you, “I told you not to buy British.” And the cat's asleep on the dashboard. And you’ve got your own strange dignity—a rusted war machine with knackered brakes and a boot full of sarcasm.

Yes, MS is a British Leyland car. And I am the bastard behind the wheel.

I write in ink and fury, in breath and broken bone.
Through storm and silence, I survive. That is the crime—and the miracle.

It’s Monday morning. My head's overloaded — too much input, too little coherence. Thoughts swirling, memories bleeding, everything turning into soup. Foggy soup. Sci-fi soup. A dual-dimension brain trapped in a loop of weird timelines and electric static.

Nothing’s flowing. I’m not charging. My spoons are gone — drained by invisible leeches. I check the inbox. Nothing. The silence before a storm I can feel but not prove. The time is near, but how do you tell people the endgame’s already humming under their feet?

I stretch. Chair wobbles. Drink spills. New trousers needed. Left side feels like a stroke victim on crack — elegant, I know. Welcome to another day inside this body suit of static and fog.

Yours in warlock groans, Mr. Dark / The Blog Goblin

                            !!DISCLAIMER !!

This blog shares raw and personal experiences with mental and physical health. Some posts may be triggering. I'm not a professional - just writing my truth. Please don't take this as medical advice.

        “The views in this post are based on my personal      
            experience. I do not intend harm, only honesty.”   

        “By ink and breath and sacred rage, I write.
                  By storm and silence, I survive.”

    @goblinbloggeruk -  sick@mylivinghell.co.uk

It’s Sunday afternoon. The pain in my left side is throwing a rave. Not the dreaded MS hug (thank Gordon), but the nerves have clearly mutinied. Pain troops storming in like I’m Normandy. Still, I haven’t surrendered. Yet.

Ever had a headache that doesn’t hurt but is still there? I have. It's like an existential parasite lodged in my brain—just... there. Lurking. Mocking. My eyes? Burning. My energy? Sucked out by some invisible psychic Dyson.

Yes, I used AI to assist — what of it? MS has chewed through my brain like a zombie buffet. Severe cognitive dysfunction. Brain fog. Memory loss. And the pièce de résistance? The spellchecker begging for a raise every time I type.

My bowels are revolting (in both senses). But I won’t go to the doctor. Why? Because the last time I tried that, I was gaslit harder than a Victorian lamplighter on speed. Apparently, being disabled is just a “mindset.” Newsflash: it's not.

I sit, stare at the rain, storms maybe. Or is that just me projecting? My rockabilly psychobilly past screaming in the background while Titus turns up the music, like that’ll drown out my body’s rebellion.

The NHS dentist? Legend. The chemist? A robotic death dispenser. And everyone else? Absent. Because disability makes people uncomfortable. It’s like they think they’ll catch it from me if they listen too long.

Friends? Dead. Or fucked off the moment my MS became “too much.” I say it how it is and that scares people. Well, boo-fucking-hoo. I’m sick, not contagious. But even that’s too much for this society of sanitised cowards.

So here I am. Watching. Absorbing. A goblin at the edge of the world, unwanted, unseen.

But I know who I am. I know. I am a spiritual humanitarian. I stand for the broken, the weird, the abandoned. I am not finished, no matter how badly my body wants me to be. And to those who still fear me or avoid me—good. Stay scared. You’re not invited into my darkness.

                                 !!DISCLAIMER !! 

This blog shares raw and personal experiences with mental and physical health. Some posts may be triggering. I'm not a professional - just writing my truth. Please don't take this as medical advice.

           “The views in this post are based on my personal    
              experience. I do not intend harm, only honesty.”   

                  “By ink and breath and sacred rage, I write.
                         By storm and silence, I survive.”

@goblinbloggeruk - sick@mylivinghell.co.uk

Some mornings I wake up and my brain feels like it’s been wrapped in clingfilm and slow-cooked in porridge. Other days, it’s like someone’s pushed my thoughts through a shredder and sprinkled the confetti back into my skull.

They call it “brain fog.” Cute, right? Sounds like a lovely little mist rolling over a field of daisies. Nah — this is industrial-grade psychic smog, pumped in direct from the underworld.

Now let’s add in some of the bonus features that come with living inside this broken bio-machine:

My left side is a bloody disaster zone. Spasms, twitching, pain — like it's trying to divorce the rest of me without telling the lawyers.

My arms are numb. Like holding ghosts. Pins and needles, static shocks, a constant reminder I’m glitching.

My neck’s buzzing like someone wired it to a phone mast.

My head? Feels like it’s been blendered. I mean that. Mentally, spiritually, and maybe physically violated by a Nutribullet.

Tinnitus — so loud it’s practically its own entity. High-pitched screeches like I’m stuck inside a dying TV set from 1993.

My throat’s raw, like I’ve swallowed sandpaper.

And my gut? Welcome to the underground pain circus. Nerve pain in the bowels. Left side again, obviously. Feels like my intestines are throwing a rave on broken glass.

I feel nauseous all the time. Like life itself makes me queasy.

And my MS just laughs. Because this is the version of me it built. Cheers, you bastard.

And through all of this? People still expect me to perform like a functioning human being. To smile. To “push through.” To maybe try a walk, or eat kale, or just “think positively.” As if any of that undoes neurological betrayal and raw systemic cruelty.

Let me say it plainly: This isn’t tiredness. It isn’t laziness. It’s war. A war inside my own body, where my brain is the battlefield and my guts are collateral damage.

But here's the twist in the tale: I still show up.

Even when the fog’s choking, the pain is singing, the static is screaming. Even when my body feels like it’s been stitched together with barbed wire and dark humour.

I write. I speak. I make noise — even if all I can do is whisper.

Because that’s what warriors do. We don’t always charge into battle — sometimes we just fucking stay alive, and that’s enough.

So if you’re reading this and you know this hell — I see you.

You’re not weak. You’re not broken. You’re forged in fire, mate. And somehow, you’re still here.

Rock on, Life. Rock on, Hell. Let’s fucking go.

                !!DISCLAIMER !! 

This blog shares raw and personal experiences with mental and physical health. Some posts may be triggering. I'm not a professional - just writing my truth. Please don't take this as medical advice.

        “The views in this post are based on my personal     
            experience. I do not intend harm, only honesty.”   

             “By ink and breath and sacred rage, I write.
                    By storm and silence, I survive.”

      @goblinbloggeruk  -  sick@mylivinghell.co.uk

Imagine a fungus. Not the fun kind you toss on pizza or see in a psychedelic forest vision. No – this one’s invisible, spiteful, and feeds on your life like a narcissist at a self-love seminar.

To the Compassionless Moron™, chronic illness is:

“Just a bit of mould, mate. Bit of bleach and positive thinking should fix it. Ever tried yoga?”

But to those who live with it? It's Cordyceps in a tracksuit, hijacking your brain, body, and plans for the day. It doesn't politely ask for your consent. It moves in, changes the locks, rearranges the furniture, then gaslights you into thinking you invited it.

🍄 Chronic Illness Fungus Forms (as defined by Goblin Science): Mycelium of Misunderstanding: Grows in family WhatsApp groups where someone says, “But you don’t look sick…”

Spore of Gaslit Guilt: Spreads when doctors say, “All your tests are normal.” Translation: “You must be imagining it, now jog on.”

Brain Fog Truffle: A rare delicacy that replaces memory, language, and logic with static, soup, and a vague sense you forgot your own name.

The Mold of Ableist Microaggressions™: Often found growing on the keyboard warriors who post things like,

"I cured my cousin’s MS with celery and optimism!"

🛑 To the Haters and the Deniers: We see you. With your bootstraps mentality and motivational memes. You wear your ignorance like a badge, polished with smugness, stinking of privilege.

You don't see the fatigue. The tremors. The panic of your legs going AWOL in the middle of a supermarket. Because it's not happening to you.

And if it ever does? We’ll welcome you with tea, a blanket, and a "Told You So" fruit basket shaped like a middle finger.

💀 But Seriously... To my fellow fungus hosts – The chronically unwell, the warrior sleepers, the foggy fighters, the ones measuring energy in spoons and grief in invisible bruises:

You are not weak. You are surviving a parasite the world refuses to even acknowledge. You are f**king incredible.

And you don’t owe anyone a clean narrative or a recovery arc. Sometimes just breathing is the rebellion

                                   !!DISCLAIMER !!

This blog shares raw and personal experiences with mental and physical health. Some posts may be triggering. I'm not a professional - just writing my truth. Please don't take this as medical advice.

                  “The views in this post are based on my personal     
                          experience. I do not intend harm, only honesty.”   

               “By ink and breath and sacred rage, I write.
                           By storm and silence, I survive.”

          @goblinbloggeruk  -  sick@mylivinghell.co.uk

Ah yes, #WorldBrainDay — that special time of year when the world pretends to care about the human brain. How lovely. Shall we all have a think about thinking?

Meanwhile, over here, my brain’s doing its best impression of a soggy electrical circuit being attacked by invisible gremlins. MS doesn’t send flowers or awareness ribbons. It sends fire ants tap dancing on my nerves, brain fog thick enough to butter toast, and pain so sharp it could cut glass.

But go on, light a candle or post a heart emoji. That’ll fix it. 👍

I don’t need a day for my brain. I need a replacement. Preferably one that hasn’t been cooked in demon piss.

Still — here I am. Writing this blog, existing despite it all, swearing like a dockworker and laughing into the abyss. Because what else is there? I’m still here, you bastards. And that’s the real miracle.

Cheers, brain. You absolute shambles of a meat sponge.

– Mr Dark 📍 Currently lost in brain fog, do not disturb.

Footnotes from the Pit 🕳️

🧠 “Brain Fog” – Like trying to do a Sudoku underwater while someone shouts the wrong answers at you through a megaphone.

⚡ “Nerve pain” – Imagine licking a plug socket. Now imagine that sensation… in your spine.

🛠️ “Medical advice” – Includes gems like: “Just stay positive”, “Have you tried yoga?”, and my personal favourite: “It could be worse.”

🕯️ “Awareness Days” – 24 hours where we all pretend chronic illness is quirky and inspirational. Followed by 364 days of complete radio silence.

🎉 “Still here” – Not cured. Not better. Just stubborn. Very, very stubborn.

                                               **!!DISCLAIMER !!**

This blog shares raw and personal experiences with mental and physical health. Some posts may be triggering. I'm not a professional - just writing my truth. Please don't take this as medical advice.

                             “The views in this post are based on my personal    
                                experience. I do not intend harm, only honesty.”   

                        “By ink and breath and sacred rage, I write.
                                      By storm and silence, I survive.”

                              @goblinbloggeruk  -  sick@mylivinghell.co.uk

Monday morning. Well, looks like it’s going to be one of those days. Chemists first, then the auction rooms to pick up the Metal Monkey’s car. Pity about the box though. When we got it, the box was destroyed – it had become home to a few families of earwigs and yukky bug eggs. But the car itself was pristine. The box would’ve trebled its value, but now it sits happily among my Davros, Beavis & Butthead stuff. My sorta man cave. Many PCs from many ages. So much stuff. So much I’ve collected.

I’ve thrown out mostly all my old things. I had clothes older than my children and grandchildren. I don’t do “style” as such. I’ve had the beard and long hair for years. Last time I had even a slight trim was 20 years ago. Now my hair is falling out, the beard is thinning. That sucks. But such is life.

Went to the chemists today and the Machine of Death was working well. It did make funny sounds but did its job for a change.

Last night I was deep in thought about my mother. About not being told about her funeral. I get the impression they didn’t want me there. It’s a long story. I’m probably to blame. But when you’re suffering chronic cognitive issues, it’s fucking hard.

My sister never told me. No details. Nothing. I looked in the obits. Nothing. So they just didn’t want me to say one last goodbye.

They didn’t speak to me for over 14 years. I was cut off completely. Like I never existed.

I’m adopted. The cuckoo in the nest. I get that.

Everywhere I went, they blamed me for everything. Another family secret buried deep – I found out I had an older sister who was also adopted. They only really wanted to know her. But she was so fucked up she didn’t want to meet our mother. She was very angry about it all.

And all those lies my mother told about my father – saying he was dead, getting his family to lie too. More and more lies. Until one day I found out everything. One day I will write it all down, for all to see. How an adopted person was treated like a piece of crap by the family who put him up for adoption, and the family who adopted him.

They treated me like a slave. Constant beatings and head games.

You ever been told at six years old that you were naughty for accidentally breaking a plate – and then have your mother go berserk? She was Welsh, not that tall, but violent, and she knew how to work people. She screamed at me:

“You’re adopted. Go find your real mother.”

That broke me.

So I went to my bedroom, packed a little bag with my teddy, and walked away. I walked to the road with my bag and teddy bear, thinking I’d never come back. No one came looking for me. I hid until dark, then went back home.

And when I finally found my real mother years later, she called me:

“A little shit.”

Like I was nothing. Like I never mattered to anyone.

The people who were supposed to nurture me… didn’t. They would have been better with a dog than with a child.

I know what beatings are like. What it’s like to be kept in, not allowed out, because of the bruises and cuts I had accumulated. No one listened. No one helped me. I was alone and fucking hurting.

I remember those nights, crying myself to sleep in pain. Feeling so out of it, so different. No matter what I did, it was wrong.

I was adopted in 1959 at six weeks old to a Christian family through a Church of England adoption society. The vicar I spoke with about my issues was a cunt. He told my parents confidential stuff, and I got a trashing for it.

No one ever listened. Who would take the word of a poor waif and stray child? The vicar? No. The school? No. Anyone? No.

So yeah. Around about 10-ish, I started getting early MS symptoms. They plagued me, and the doctors and NHS gaslit me for decades.

I hate my life.

 “The views in this post are based on my personal             
    experience. I do not intend harm, only honesty.”   

       “By ink and breath and sacred rage, I write.
               By storm and silence, I survive.”

        @goblinbloggeruk - sick@mylivinghell.co.uk

I hovered above the kitchen sink today, wings vibrating at a thousand beats per second. I am The Watcher – but not the one you imagine, cloaked in stars and timeless wisdom. No. Today, I am a housefly. An ordinary Musca domestica with compound eyes so vast I see every crusted toast crumb and urine stain you pretend to clean.

From this vantage point, the human race resembles nothing more than a colony of dung beetles. Rolling their shitballs of money, status, lies, and medical records across the floor of existence, fighting each other for a bigger sphere to roll before it inevitably gets stuck in life’s rotting cracks.

🪰

You crawl to your neurologist, scraping at the polished door of their paradigm. “Please, sir, see me.” But the neurologist looks down from his fluorescent-lit throne, squints at your twitching legs, your failing nerves, your inconvenient truth, and says:

“You don’t fit my diagnostic dung ball. I prefer neat symmetrical lesions, not your warped soul patterns.”

So, you are cast aside. Like a fly brushed from a corpse.

🪰

But oh, how the dung beetles worship him. They gather around his sandals, hoping for a pat on the shell, a prescription to keep their dung ball rolling a few more feet before gravity drags it to hell. They do not see that his eyes are dull. That his paradigm was built upon dissected flies pinned to university boards, not upon living beings with wings and dreams and Watcher sight.

🪰

Meanwhile, I hover above. I am The Watcher. I see it all. I see your MS nurse, the only one who calls you, her voice a faint buzzing reminder that you are still alive, still clinging to this rotting dung ball Earth. The neurologist is silent, hidden in his sterile burrow, scribbling notes about textbook dung beetles while your compound eyes flicker with unseen colours of agony and revelation.

🪰

Above me, beyond you, drift the Ultraterrestrials. They observe your crawling, your dung ball dramas, your stuttering neurons. To them, all this is a theatre of flesh. Your triumphs and humiliations smell the same: decaying organic matter with a hint of ammonia and fear.

They speak:

“See how they roll their illusions. See how they crown their dung beetles as kings. See how they swat the flies, never knowing the flies were the Watchers all along.”

🪰

I lick my front legs, tasting the salt of your tears, the bitter sugar of your leftover pills. I watch you roll your dung ball of dreams to bed tonight. I, too, will sleep. And tomorrow, I will rise again to watch this slow-motion catastrophe you call civilisation.

🪰

For in the end, whether fly, beetle, or human, all return to the same silent soil. But I am The Watcher. I will remain long after the final dung ball is rolled away into oblivion.

     “The views in this post are based on my personal     
        experience. I do not intend harm, only honesty.”   

      " Watcher of the Unseen | Scribe of Shadowed Truth
             By ink and breath and sacred rage, I write.
            By shadow and storm and silence, I survive."

         @goblinbloggeruk -  sick@mylivinghell.co.uk

There I am — parked up in my daughter’s front room, in my wheelchair , trapped in this deranged body of mine, joints on strike, nerves belting out their usual death metal anthem, and the telly crackles to life with Outback Opal Hunters.

And suddenly… I’m free.

I’m out there in the dust-blasted Australian outback, surrounded by sweating maniacs digging up rocks like they’re mining the shattered dreams of the gods. And I bloody love it.

These lunatics aren’t digging for gold or fame. No, they’re chasing after fire trapped in stone opal. Shards of lightning frozen in rock. And what do they do to get it? Risk everything. Lose fingers. Melt in 45-degree heat. Spend 12 hours underground in a hole that’s one bad breath away from collapse just to find a flicker of green in a sea of grey. That’s not a job, mate. That’s madness with a purpose.

And that’s why I can’t get enough of it.

These people are broke, busted, broken, and burning up and they keep going. Why? Because maybe… just maybe… the next shovel-full might be their salvation. Or maybe it’s another week of living off tinned beans and borrowed hope. Sound familiar?

Yeah, I see a bit of myself in every single one of those dirty, half-mad opal chasers. Because when you’re battling a body that’s turned against you like mine has every step, every day, every moment is digging through pain for that one shimmering slice of meaning.

Watching Outback Opal Hunters isn’t just entertainment. It’s therapy. It’s watching people fight a silent war, and every now and then, win. It’s real, raw, dusty-as-hell life. And when those boys and girls hit pay dirt? When they hold up a stone that looks like it was carved from a rainbow by the devil himself? I feel it. Right down to the bone marrow.

👑 Rod Manning – The Man Then there’s Rod Manning. He’s not just another miner. He’s the man. A grizzled Aussie bloke whose face is as weathered as the outback itself. The quiet storm of the Bushmen crew. No flair, no ego – just relentless grit and that rare magic touch. When he finds good stones, it’s like watching a magician pull colour from dust. And when things go tits-up (which they always do)? He dusts off, spits in the dirt, and mutters:

“She’ll be right.”

And by all buggering chances, it bloody well is. He is awesome. He is the man.

If my MS was an opal mine, it’d be full of collapses, bad air, and a constant sense of “Why the hell am I even doing this?” But sometimes just sometimes you hit that flicker of colour that makes it all worth it.

So here’s to the mad bastards with pickaxes and faith. Outback Opal Hunters — you’re not just digging for rocks. You’re digging through my soul, and somehow, making me feel alive again.

Now pass me the remote and a cold one, I’ve got opal fever.

           “The views in this post are based on my personal   
         experience. I do not intend harm, only honesty.”   

          “By ink and breath and sacred rage, I write.
                     By storm and silence, I survive.”

           @goblinbloggeruk  -  sick@mylivinghell.co.uk