Multiple sclerosis  is My Living Hell

DarkHumour

All posts tagged DarkHumour by Multiple sclerosis is My Living Hell
  • Posted on

    Well then. Off out we go. A grand expedition. An odyssey, no less. All the way to the garage—yes, that mystical temple of greasy doom—to get the old van MOT’d. It’s not just a vehicle, it’s a relic. Twenty years of loyal service. Mostly. Bit of rust. Bit of creak. Bit of “please God let it start.” But it’s still here. Like me. Hanging on out of pure spite.

    Someone once said, “They don’t build them like that anymore.” And thank Christ for that. If cars were still made like they were in the 1970s, we’d all be broken down on the M1 watching steam pour out the bonnet, while some bloke in flares offered to tow you with his Cortina estate. Those cars were about as reliable as a wheelchair battery in a thunderstorm.

    I remember when the UK was littered with RAC and AA phone boxes—those little yellow lifelines dotted along motorways. They’ve vanished now, like empathy, sanity, and the NHS. Rare as hens’ teeth, or an honest politician.

    Anyway, I didn’t sleep last night. Not a wink. My bladder decided it was time to act out a scene from Backdraft. I lay there, staring into the ceiling void, pissing every twenty minutes like a possessed lawn sprinkler. So I started thinking—because what else do you do at 3am when you're soaked in fatigue and futility?

    I thought about all the crap cars I’ve owned. So many. Too many. If there were a museum for motoring misery, I’d be a patron saint. Rattling doors, broken electrics, heaters that blew cold air in summer and hot air in hell. The British car industry, ladies and gentlemen.

    But let’s rewind. Before the wheelchair, before the rust bucket van—I was a biker. A proper one. Big beard. Long hair. Leather jacket that smelled of oil, rain, and barely controlled aggression. Speed. Freedom. The road was mine.

    That all changed the day I hit a loose drain cover on a damp road. Back end of the bike went out from under me. Hit the tarmac like a sack of angry potatoes. And I got up. Physically. But something in me didn’t. Something silent and final shifted. I realised, I can’t ride like this anymore.

    But I wasn’t ready to give it up. Not then. So I bought another bike. Custom triked it. Spent a fortune on it—my last defiant middle finger to the creeping MS. I rode that beast as long as I physically could. Until one day, even mounting it was like scaling Everest. Body said, “You’re done, mate.” And I knew it was right.

    I sold the trike two years ago. That was the last real ride. The final roar of the engine before the silence set in. Felt like watching a part of myself being towed away behind someone else’s smile.

    And now? Now I’m being slowly retired by force. Out of work. Out of energy. Out of options. Soon to be ejected into the bureaucratic black hole of the state pension. My business—what’s left of it—will die the day I clock off. I can feel it gasping already. I went to uni at 40. Built something. Pushed hard because I knew I had a window. Now the window’s shut and the room is on fire.

    Truth is—I haven’t been properly “capable” in years. Five, easily. These days I just sit, staring into the abyss, waiting to see if anything interesting crawls out. So far: nada. But I’m still here. Just about.

    Still, I did things. Things I never thought I could. That’s the weird joke of it all. Even while your body’s disintegrating, there are moments—real moments—where you do something good. Where you matter. But that only happens if you’ve got people around you who actually care. No gaslighting. No clipboard psychology. Just real help. The kind that doesn't end with “There’s nothing more we can do.”

    Oh yes. Been told that more times than I can count. It’s medical code for “You’re a problem we can’t fix so piss off quietly.” They said it like they were reading the weather. I left those rooms devastated. Angry. Broken. But not done. I still had enough fight to ride out of there burning with fury.

    Then I remembered my students. I used to teach adults with learning disabilities. You know, the people society would rather not look at. The ones who get shoved into corners, behind policies and forgotten services. And let me tell you—they were the most genuine, honest, loving people I’ve ever known. No hate. Just humanity. And we broke them. We broke them too.

    And now? Now I’m gearing up for the next tiny battle: getting dressed and into the van. It’ll take hours. Every task is an assault course. But I’ll do it.

    Because I always fucking do.

                          “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.”
    

    enter image description here

                            @goblinbloggeruk - sick@mylivinghell.co.uk
    
  • Posted on

    Sat here mumbling into my old iffy microphone today. Took me over a day to set up – drivers, updates, reinstalling Windows three bloody times because my brain fog decided to overwrite the system with a random USB stick. Genius, I know.

    Finally, the blog goblin’s computer has resurrected. Barely.

    Had yet another bad night. Partly my own fault this time. Thought I was the biker prophet and magically healed, so decided to stand up and shuffle furniture around like some nocturnal DIY hero. Clearly not my best idea. Lost my balance entirely, stumbled like a drunk, and smashed into the door frame.

    My shoulder’s killing me, bruised to hell, and possibly broken. Will probably end up in A&E later if it gets worse. For now, just sat here typing, all fingers and thumbs, trying to find old bits to post while ignoring the pain.

    Having MS makes me resilient, though. Even when my brain is fried and my body’s screaming betrayal, I keep crawling back like the stubborn goblin I am.

    Anyway. Hope your day is glitch-free and you aren’t slamming yourself into any door frames. Unlike me. 🖤

        ⚡️ Join the gremlin cult. You know you want to
    
      " 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.”
    

    enter image description here

                           🧌✨ @goblinbloggeruk ✨🧌
    
  • Posted on

    If You Could See MS – You’d Probably Run Away

    People love to say “You don’t look sick.” Oh, don’t I? I’m sorry. Next time I’ll crawl in covered with barbed wire and nails through my feet so it’s easier for you to grasp.

    Because if you could actually see multiple sclerosis, it might look like this:

    Legs wrapped in barbed wire so every step is agony, but I still smile politely because God forbid I make you uncomfortable with my pain.

    A back covered in spikes, each one representing burning nerve pain, tingling, numbness, and a touch of “Did I leave the oven on or is my brain just fried today?”

    Feet impaled with nails, but I’m still expected to do the shopping run and act like “walking it off” is an option.

    Fatigue so crushing that holding a coffee cup feels like lifting a bus – but yes, tell me again how tired you are because you stayed up watching Netflix.

    Sticky notes of toxic positivity slapped all over me screaming “You can do it!” when honestly, no, sometimes I bloody well can’t.

    A silent membership in the Broken Dreams Club, because chronic illness isn’t just physical – it devours futures, careers, friendships, and everything you thought you’d be.

    If you could see MS, you’d probably look away, change the subject, or thank your lucky stars it’s not you.

    But guess what? This is the reality we wake up to every single day. And no, it doesn’t take a day off.

    Why It Matters Multiple sclerosis is an invisible illness. People don’t see the pain, the muscle spasms, the loss of balance, the cognitive fog, the sheer mental toll of fighting your own body every waking hour.

    You just see us standing there. Smiling. Nodding. Pretending we’re not screaming internally.

    So Here’s To Us To every MS warrior carrying these invisible barbs and nails: We see each other, even if the world never will.

           “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.”
    

    enter image description here

                              🧌✨ @goblinbloggeruk ✨🧌
    
  • Posted on

    Top Ten Alternative Medicines: Because Desperation is Expensive Let’s face it. When mainstream medicine gives you nothing but side effects, gaslighting, and a mild death wish, you inevitably end up here: the world of alternative medicine. Welcome to the land where hope meets your bank balance, and your sanity politely exits stage left.

    Here’s my brutally honest ranking.

    1. Acupuncture 💉 Claim: Sticking needles in you realigns your life force. 💀 Reality: You’re paying someone to stab you repeatedly. Might help pain a bit. Might just remind you you’re alive, which is arguably worse.

    2. CBD / Cannabis 🌿 Claim: Cures everything from pain to your failed marriage. 💀 Reality: Can ease pain, spasticity, and anxiety. Also makes you realise how soul-crushing your life is with exceptional clarity. Worth it.

    3. Reiki 👐 Claim: Someone waves their hands near you to shift energy fields. 💀 Reality: Basically spiritual WiFi with zero scientific backing. Still, lying still for an hour while someone hovers over you is strangely calming.

    4. Herbal Teas & Tinctures 🍵 Claim: Plants heal. 💀 Reality: Some herbs genuinely help mild symptoms. Others taste like compost water, make your bowels explode, and cost more than your rent.

    5. Homeopathy 💧 Claim: Dilute poison to cure poison. 💀 Reality: Sugar pills with memory water. Useful only if your illness is a placebo in the first place.

    6. Crystal Healing 💎 Claim: Rocks vibrate healing energies. 💀 Reality: They look pretty on your shelf while your body continues its daily betrayal.

    7. Aromatherapy 🌸 Claim: Oils fix everything. 💀 Reality: Lavender might calm you. Peppermint might help your headache. But no oil will fix your soul-crushing fatigue. Sorry, Karen.

    8. Reflexology 🦶 Claim: Pressing your feet heals your organs. 💀 Reality: Great foot massage. Everything else is foot-based fan fiction.

    9. Ayurvedic Medicine 🪷 Claim: Ancient Indian herbal wisdom balances your doshas. 💀 Reality: Some legit herbal remedies. Some unregulated heavy metal pills. Roll the dice and hope you don’t get arsenic with your ashwagandha.

    10. Hypnotherapy 🌀 Claim: Reprogram your subconscious to fix illness, pain, trauma. 💀 Reality: Helpful for stress or trauma-based conditions. For MS nerve damage? Might as well hypnotise yourself into believing you’re a golden retriever for emotional support.

    Final Thoughts Will any of these cure your incurable chronic illness? No.

    Will they make life slightly more bearable? Some might.

    Will your bank balance survive this spiritual capitalism? Absolutely not.

             “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.”
    

    enter image description here 🧌✨ @goblinbloggeruk ✨🧌

  • Posted on

    🖤 “ coming Soon: A brutally honest ranking of the top ten alternative medicines.

    What’s worth it, what’s useless, and what might just make life with chronic illness slightly less unbearable.”(Straight but brand-consistent) “Soon: A brutally honest ranking of the top ten alternative medicines. What’s worth it, what’s useless, and what might just make life with chronic illness slightly less unbearable.”(Straight but brand-consistent) “Soon: A brutally honest ranking of the top ten alternative medicines. What’s worth it, what’s useless, and what might just make life with chronic illness slightly less unbearable.”

    So, you’ve got MS. Congrats on your new life sentence. Welcome to the club nobody wants to join, where your immune system treats your nerves like a chew toy and daily tasks become extreme sports. If you’re wondering how to cope with the relentless mental and physical torture that is Multiple Sclerosis, here’s your brutally honest, darkly comedic guide.

    1. Eat Like You Actually Care (Even Though You Don’t) Sure, nutrition might help reduce fatigue, inflammation, and general bodily betrayal. Will quinoa and kale cure your MS? Absolutely not. But it’ll help you feel morally superior while your nervous system crumbles.

    2. Exercise Without Dying Yes, exercise is important. But if you’re one squat away from sh*tting yourself or collapsing like a Victorian woman denied her fainting couch, maybe start with gentle stretching or a walk to the fridge. Small wins.

    3. Train Your Brain (Before It Leaves You) MS can fog your mind faster than three bottles of wine. Crosswords, sudoku, brain training apps – all designed to slow the brain-melt. Bonus: if you forget to do them, that’s probably why you need them in the first place.

    4. Sleep: Because Insomnia Isn’t Edgy MS fatigue is like dragging a corpse around all day. Insomnia makes it worse. Try regular sleep times, a dark cave-like room, and cooling your room so your inner demon feels at home.

    5. Stress – Your Favourite Symptom Trigger Stress is the invisible gremlin that pokes your MS into full meltdown. Meditate, do yoga, or scream silently into your pillow. Whatever keeps you from becoming an actual murderer today.

    6. Vitamin D & Smoking Low vitamin D makes MS worse. Smoking makes MS worse. The universe is basically telling you to quit cigs and take a supplement. Or keep smoking and accept your fate – dark choices only you can make.

    7. Heat: Your Mortal Enemy Heat turns your already dysfunctional nerves into cooked spaghetti. Stay cool. Cold drinks, fans, icy glares at strangers – all recommended.

    8. Depression & Anxiety: The Cherry on Top MS is a daily trauma loop, so depression and anxiety are loyal companions. Therapy, meds, and dark humour memes help. Talking to people might too, if you can be arsed.

    9. Alternative Therapies Massage, acupuncture, cannabis oil – none will resurrect your dead nerves, but they might make the pain less unrelenting. Go wild. Or don’t. It’s your hell.

    Final Pep Talk MS won’t kill your dark sense of humour, unless you let it. Implement these daily management tips and maybe – just maybe – tomorrow will suck slightly less.

           “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.”
    

    enter image description here

                              🧌✨ @goblinbloggeruk ✨🧌
    
  • Posted on

    So, you’re thinking about medical cannabis? Congratulations on reaching that inevitable point where life hurts so much you’re ready to pay £200+ a month to not want to punch everyone in Tesco. Welcome to the club.

    Here’s everything you need to know about getting a prescription for medical cannabis in the UK – because apparently, the NHS thinks your suffering is adorable, but not quite “let’s fix it” adorable.

    1. Is it even legal? Yes. Medical cannabis has been legal in the UK since 2018, but don’t get too excited – it’s not like they’re handing out joints at your local GP. Only specialist doctors prescribe it, and mostly through private clinics. Around 20,000 people have prescriptions. Think of it as an exclusive club for the perpetually pained.

    2. What can it treat? Mostly chronic pain, but also PTSD, anxiety, OCD, autism spectrum disorder, ADHD, and the general misery of existence (unofficially).

    3. Am I eligible? If you’ve tried at least two medications that didn’t work, and you’re not actively hallucinating demonic squirrels daily, you’re probably eligible. A specialist will decide. GP referral is nice but not required. Just another British system that rewards stubborn self-navigation.

    4. How much does it cost to feel slightly less sh*t? Consultations: £49 – £200 depending on clinic greed.

    Prescriptions: £200 – £300/month for flower (oil costs more).

    Total: Think of it as your new rent payment for your brain.

    Some clinics have access schemes like Project Twenty21 to reduce costs if you’re happy being studied like a stoned lab rat.

    1. The 5-step process to blissful legality Step One: Choose a clinic About 20 private clinics exist. Some focus on chronic pain, others on mental health. Shop around like you’re choosing a funeral director – carefully and with low expectations.

    Step Two: Eligibility assessment They’ll ask for your medical history via a form or short virtual call. Most get approved unless there’s a serious safety concern (or you call them a c*nt mid-call).

    You’ll need your Summary of Care records from your GP. Prepare for the NHS receptionist to act like you’ve requested the nuclear codes.

    Step Three: Initial consultation Here you tell them:

    What’s wrong with you (everything)

    What you’ve tried (everything)

    If you’ve used cannabis before (it’s fine, they don’t care)

    What you expect from it (relief, obviously)

    They’ll probably start you on oil, because flower = scary government panic.

    Step Four: Choosing a pharmacy Clinics usually have a pharmacy they use, but you can take your prescription anywhere that dispenses medical cannabis. Your weed gets couriered to your door within 48 hours of payment, unless the UK postal gods decide otherwise.

    Step Five: Follow-up consultation One prescription per month = one follow-up per month. Adjust dose, repeat the ritual, pray for relief, try not to commit murder in the meantime.

    1. Final thoughts If it works, great. If not, at least you tried. Medical cannabis isn’t a miracle cure, but for many it means life becomes slightly less of a living hell. And isn’t that all we’re really aiming for?

    Give it at least three months to figure out your dose before declaring it pointless – because sadly, your endocannabinoid system didn’t come with an instruction manual.

    ⚠️ Disclaimer: This is not medical advice, just my darkly honest take. Consult your doctor or your dealer’s dealer’s dealer before making changes to your meds.

         “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.”
    

    enter image description here

                      ✨ @goblinbloggeruk ✨
    
  • Posted on

    You’d think buying a watch is simple. You choose one. You wear it. It tells the time. Job done.

    Nope.

    Instead, it’s a full-scale psychological assault. Amazon probably thinks I’m running a black-market watch dealership by now with the amount I’ve sent back.

    All I wanted was a watch that:

    Tells the time

    Tells the date

    Has a big face so I can see it

    Doesn’t require a PhD in Chronology to set it up

    Instead, I got:

    ⏰ Knobs that have a life of their own, turning randomly like a possessed ouija board.

    ⏰ Buttons that demand fingers with precision I no longer have, thanks to numb hands that make the simplest task feel like I’m defusing a bomb underwater while blindfolded.

    In the end, I went atomic. Or “atomik”, as I now call it to sound edgy and slightly deranged.

    This atomic watch apparently speaks the time and date. Brilliant, I thought. It arrived, promising “easy setup” in the advert. 😂 Easy setup my arse. It took Albertine several hours of cursing to set up. She’s my go-to tech guru when life’s gadgets decide to humiliate me, and even she looked ready to launch it out the window.

    I just sat there, numb hands useless, staring at it and laughing like a lunatic while she pressed random buttons in despair.

    But hey, it works now. It talks to me. It’s large enough to see. And it hasn’t tried to kill me in my sleep yet. So it’s a win. Kind of.

               “By ink and breath and sacred rage, I write.
                         By storm and silence, I survive.”
    
         “The views in this post are based on my personal
          experience. I do not intend harm, only honesty.” 
    

    enter image description here 🧌✨ @goblinbloggeruk ✨🧌

  • Posted on

    Another system rebuild. Another round of pretending this time it’ll work, that nothing vital will vanish into digital smoke. Maybe I’ll stick with Windows 11—just long enough to hate it all over again. Or maybe, finally, I’ll throw myself into Linux like a man falling from a burning building. Kodachi. Mint. Whonix. Take your pick, all flavours of escape.

    The plan? Dual life. Linux on a pen drive for when I need stealth and sanity. Custom Windows on the main drive for when I need chaos and legacy apps. But before anything happens, it’s backups. Backups of backups. Then backup the backup of the backup.

    I’ve lost too much already. Files. Art. Music. Decades of moments. Things that mattered. Gone because I trusted the wrong hard drive, or hit “yes” on a prompt I didn’t read at 4am because I couldn’t sleep from the pain—or the thoughts. Terabytes lost to time and stupidity.

    I’ve been part of this madness since the early 80s. When computing still felt like rebellion. When you could feel the electricity in the keys. Back when 40GB was god-tier and 32MB of RAM could change your life. When you didn’t need permission from five corporations to run software.

    Today, I did get out. Ended up at Fat Tony’s. Sex toys, incense, grinders, masks, and the surreal scent of liberation in the air. I could feel the laughter in my bones. Albertine grabbed a few curious bits and pieces. Good man behind the counter. Real. No masks. No script. Not like the world outside. Not like doctors.

    Came back home. Wheelchair of death started vibrating like it had unfinished business with the earth’s core. Loud enough to wake the ghosts I wish I could forget.

    The jam was a mistake. No sleep. Peeing every hour. Kidney screaming. Bladder playing drums. Night’s silence broken by the symphony of my body's decline.

    I asked the doctor for sleeping tablets. He laughed. Said I might sleep through an accident. “What,” I asked, “like shit myself?” He didn’t laugh back. Just stared at me like a creature in a tank. Something dying slowly behind glass.

    That same doctor once told me there was nothing more they could do. I rolled out of that office in my chair and into the hallway of despair. Slammed into the door just to feel something. I wasn’t a person to him—just another file closed. “Mr Goblin,” he said. As if I wasn’t already invisible.

    You think it ends there?

    I got a phone call years ago. I was stressed. The voice on the line? A GP. He tells me, flatly: “Oh yeah, you had a heart attack at some point.” Like it was the weather. Then the line goes dead.

    I went ice cold. Started spasming. Couldn’t breathe. Ambulance was called. Paramedics came. One looked like death in a hi-vis vest. He barked at me about not labelling my door clearly enough. I nearly told him to check my pulse and guess the address that way.

    ECG said yes, it happened. A “heart event.” Another ambulance came. The serious kind. They jabbed, they drugged, they stabilized the mess I was.

    But in that moment, on the floor, shaking and half-naked, I thought: So this is how it ends. Alone, misunderstood, staring at the cracked ceiling while the world rushes by outside.

    But no. I lived. Again. Like I always bloody do.

    And still my mind drifts. My half-sister. It’s been 10 years. Maybe she thinks of me. My older sister? Try 30. A lifetime of silence.

    Being adopted is a lifelong mind-fuck. You're the cuckoo in someone else’s nest. A mistake nobody admits. A problem to be hidden in a file folder somewhere.

    My family judged me because I lived in a council house. Because I was disabled. Because I wasn’t their version of clean or proper.

    But when they gave me a chance, I proved them wrong. Every time.

    Still… no calls. No letters. No visits.

    I wonder if my brothers are still alive. I wonder if they’d remember my voice.

    But hope is a slow suicide. So I smile instead. Laugh when I can. Back up my data like I’m guarding a soul in binary. Sit in my chair and watch the world pretend to care.

    I’m not done yet.

    Not by a long shot.

    Goblin still here

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

    looking to buy a second hand q100 wheelcair or similar in the south west area as mine has gone completely to the breakers yard in the sky ... many thanks sick@mylivinghell.co.uk

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

    enter image description here

  • Posted on

    It was over 30 years ago — but this horror never really leaves you. Like an ex with teeth, it's always in the background. This is my catheter initiation, and yes, it’s every bit as bad as it sounds.

    So, picture this: it's a hot, stressful afternoon. I'm self-employed, sweating it out, holding together life with string and sarcasm. Fast forward a few decades — now I languish on Universal Credit. MS (Multiple Sclerosis) does that. You ramble. You lose the thread. Your bladder decides it's not on your side anymore. And you get a visit from... The Bowel and Bladder Nurse™.

    She came in like Judge Judy's meaner cousin. Silent, judging, late middle-aged, seen it all, smelled it all. I’m a tall bloke with tattoos, piercings — basically a walking episode of "What Not to Bring to Your Urology Appointment.” She didn’t like me. That was clear. It was mutual.

    Fired questions at me like she was being timed by MI5. Eventually scanned my bladder and declared, “Go on, have a wee.”

    Now, I don’t know if you’ve ever tried peeing on command under pressure — but it’s up there with defusing bombs. Naturally, nothing came. She looked disappointed, like I’d failed some secret test. Her solution?

    Her solution? “You’ve not emptied. We’ll have to catheterise.”

    She pulled out a tube — a foot-long medieval torture device. It looked like it came from the same catalogue as plumbing snakes. I looked at her. She looked at me. No gloves, no chat, no dinner first.

    Panic. Stress. Dignity out the window. I insisted on doing it in private. She reluctantly agreed, still glaring like I’d stolen her cat. So into the lav I go. Now imagine pushing a thick plastic cable down the eye of your penis while sweating and crying inside. It didn’t just hurt — it screamed. Blood. Pain. Liquid betrayal. I returned to her like a war veteran holding the remains of my soul.

    “Oh,” she says. “Wrong catheter. You’ve got an enlarged prostate. Should’ve been a curved one. That size’s a bit thick.” Cheers for the heads-up. You couldn’t have led with that?

    (For the record — I used THC/CBD oil, prostate back to normal. Do your own research, obviously. Not medical advice, just bitter experience.)

    I never went back to her. But years later… the next nurse made her look like Mother Teresa. That, my friends, is a story for another post.

    looking to buy a second hand q100 wheelcair or similar in the devon cornwall area as mine has gone completely to the breakers yard in the sky ... many thanks sick@mylivinghell.co.uk

                “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.”
    

    enter image description here

  • Posted on

    It’s funny, isn’t it? You’re in a room with one other person. Just the two of you. You speak. Your mouth moves. Actual words come out. But somehow… nothing lands. It's like you're a ghost, a passing breeze, or worse — background noise to someone else's ego monologue.

    Welcome to my reality: Selective bloody hearing.

    Let me paint the scene. You're fighting off a brutal illness, spasms hit like a freight train, your brain fogs up like a broken kettle left out in the English drizzle, and then comes the cherry on top — people don’t listen. Not can’t. Won’t. They avert their eyes, mumble condescending clichés, or — the fan favourite — promise they’ll “call you soon.” (Spoiler: they won’t.)

    Is it the wheelchair? The drooping face? The occasional dribble? Or do they just prefer their disabled friends silent, motionless, and conveniently non-existent?

    Maybe They’re Just Uncomfortable? Oh yes. Heaven forbid they feel awkward while you’re being eaten alive by something terminal and nightmarish.

    I started calling them out. Can you imagine the chaos? Apparently, honesty from the terminally ill is too real. It makes dinner parties awkward. And honestly, I’m well past the point of caring. If I’m going to be ignored, I might as well scream in Black Sabbath and let Ozzy do the talking.

    Paranoid? Nah. At first, I thought maybe it was just me. A bad day. A misread signal. But no. There’s a pattern. The looks. The empty promises. The slow fade-outs. The way friends evaporate like cheap aftershave. You become a "thing," a problem they can't fix and don't want to look at. I didn’t ask to be a medical freakshow — but here I am, feeling like the last carnie in a ghost-town circus.

    It's Raining, I'm Buzzing Brain fog is a beast. Been digging into DNA research (who was I before this monster arrived?), but my head’s a bag of wet socks lately. Tingling lips. Numb tongue. Probably allergic to the air again. And that damn straw — it always goes missing, like some household Bermuda Triangle.

    Wrestling Is My Religion Say what you want — yes, it’s “fake” — but pro wrestling is realer than most people I know. There’s truth in the ring. Pain. Theatre. Keyfabe. Art. The ghosts of the squared circle still dance under the spotlights in my head. And let’s be honest, “Real life is fake. Wrestling is real.” That’s my gospel. That’s truth.

    📢 Follow me on X/Twitter: 💀 “If you like your humour dark and your truth darker, come hang out with a chronically ill goblin on a ranting mission of mayhem. Pro wrestling, spirituality, weirdness,disability, sarcasm, and survival served raw.”

    🧠 @GoblinBloggerUK 📍 Because somebody's got to say it...

                  “REALITY IS FAKE. WRESTLING IS REAL.”
                                — @GoblinBloggerUK
    

    looking to buy a second hand q100 wheelcair or similar in the devon cornwall area as mine has gone completely to the breakers yard in the sky ... many thanks sick@mylivinghell.co.uk

             “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.”
    

    enter image description here