progressive MS

⚠️ 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 professional help.

So I suppose I first started smoking marijuana when I was a teenager way back in the 1970s experimentation and all that stuff. And it was a very pleasant effect, I must say. I stopped smoking when I got married, I didn't find it did anything untoward to me but there we go.

Anyway, about five six years ago I believe I decided to look into marijuana again and how it would affect my multiple sclerosis and also the THC oil as well. So, I did a lot of research and I spoke to a lot of people all over the world who had been using marijuana and THC oil to combat the effects of their multiple sclerosis.

The reasoning for this is that I do not like taking opioids as they turned me into a total zombie. And it seems that all of the big farmer stuff I get from the doctors, if there is a side effect on the packet, I usually get it. That's the problem. My body is so damn sensitive to everything.

That's why I went down the route of medical marijuana and THC -cbd oil I had heard from my MS nurse that marijuana, medical marijuana, was legal for people with illness in the UK. As the MS nurse had just come back from the conference and gave me the address of a website....

I looked at the website in slight disbelief thinking, "Oh my gosh! Medical marijuana legal in the United Kingdom and THC CBD oil. That literally blew my mind." And then I looked on the website and, well, it asked some simple questions and I followed the questions and gave my answers and whatnot.

I sent my records, my medical records, that is to the clinic and then I was given a consultation and after the consultation and after the reading of my medical records and everything, they then put me on THC, CBD oil. I sent my records, my medical records, that is to the clinic and then I was given a consultation over zoom and after the consultation and after the reading of my medical records and everything, they then put me on THC, CBD oil and the flower, which is marijuana oil and the flower, which is marijuana.

I get my medical marijuana and THC oil delivered. It's a good system and I do recommend that you get in contact with one of these clinics as they really do help and they really do know what they're on about. I use the Sapphire Clinic in the UK and they are very good, very caring and listen. Yes, I know you have to pay for the consultations, but it is really well worth it. They don't rush you and they take time to understand what you're talking about. So yes, I would say it is amazing, brilliant and it has changed my life for the better.

"Exactly. How did medical marijuana and THC oil help me

Well exactly where do I start? How many accidents did I have? Well the spasms are... 50% gone. And it was the spasms that caused me to break more bones in my body than you could believe. Before I was in the power chair, I used to use sticks and I used to get such severe spasms that my legs, well I'd kick things for no reason. It's like oh look there's a dust bin and bang I would just kick it Yes, you guessed it. I have broken every toe on My both feet my God. It's absolutely a nightmare.

The bruising the matter nails that came off Yes, so it is really bad news and Luckily, I haven't had those massive bad spasms anymore I've kicked doors door frames God knows what and it's bloody painful. That's for sure I've walked into door frames, I've concussed myself, God knows how many times when I've walked into things. Oh my God, I was like a walking accident waiting to happen.

The thing is you still think you can do everything even when you can't and when you try it always results in an accident with me. It's not very funny but it's true. But I have since realised that being safe, being careful is the best way. Anyway, I'm getting off the subject that I was on about. So the CBD oil and the flour helped me with my spasms, helped me with my pain, they helped me just be me, they helped me relax, they helped me sleep, they make my life happier. I would say that I am more aware.

I don't suffer the off my head side effects as I've been smoking it for nearly what, five years now. So it doesn't affect me like that. So yes, it is very strange, but it really does work. It really does get rid of a lot of the pain. And then you don't have to suffer all the constipation and all the other side effects that tablets may have on you like it did me.

Switching to medical marijuana and THC oil was the best thing that I have ever done in my life and yes I know that some people might think oh dear it's a drug and it leads to other things. Well I can assure you it does not lead to other things it is not a gateway drug for me I use it specifically medically I don't even drink alcohol and I don't smoke tobacco So, the bottom line is, it just depends on who you are and how you feel about things, to be fair. Me, I thought, well, I've got to try this because I was going downhill at a rate of knots. That is unreal.

Progressive MS is not a nice thing, and I have this histamine reaction thing which causes me even more problems with my vagus nerve, and then there's my autonomic dysfunction. You know, all these things, it's just mad, and then I have heart issues. So, yeah, the THC CBD is helping me, and personally for me it works. It might not work for other people, but there we go. That's my living truth. And I think really it's up to the person, but you should always seek medical help first before you go down that route and do some research.

some useful links below to help maybe on your journey

curaleaf clinic

ms society

Cannabis and multiple sclerosis

Warlock Dark Chronic illness survivor, truth-teller, occasional bastard. From My Living Hell (For those who came here by accident: yes, my living hell is real. And yes, we still fight. Every shitty day. With defiance.)

@goblinbloggeruk - sick@mylivinghell.co.uk 𒀭𒊩𒆳 ᛞᚱᚨᚷᛟᚾ ᛏᚱᚨᚾᛋᚲᚺᚱᛁᛖᛞ ✦ ᚹᚨᛏᚲᚺᛖᚱ 𒀸𒀭 ᚢᚾᛒᛟᚢᚾᛞ

⚠️ 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 professional help.

Ah, Monday. Everything in my body decided to go berserk overnight. MS? Revving its engine like it’s auditioning for the grand tour. Neck bone growths pressing on nerves? Check. An X-ray from ten years ago says hi. Time to see the doctor, I suppose if I survive the existential dread of the waiting room.

Strangulation sensations, head blips, tongue spasms oh, and the sweet bonus of not being able to catch my breath. Honestly, my body’s doing the kind of mad shit that would make anyone else file a formal complaint. I pity the doctors and nurses who have to deal with me. Truly. But hey, life’s a circus.

White‑coat syndrome is my sidekick. I talk to medical staff like a squirrel on espresso: chaotic, twitchy, and unintentionally antagonistic. My solution: write everything down. Hand the chaos over in neat little bullets. Works great—until I forget, which is pretty much guaranteed, and then I’m a full-blown, stressed-out disaster. Doctors are busy, complicated cases suck, I get it.

I’ve tried it all. Meds? Side effects so bad my body staged a protest. Seven-day hospital admission? Almost happened, but I said “fuck it” and walked. Holistic methods, lifestyle overhaul, mind-body-soul cleanse—my own brand of chaos control. Fix? Plumbstick there isn’t one. Options? Sure. Natural? Works for me.

Present me? Ambivalent, tethered to this illness 24/7. Tinnitus now “harmonizes” with Blondie, which is absurdly funny if you squint. Yopi is decompressing, slowly realising this is a loving home and not just a mildly terrifying human experiment. Fingers tingle. Tips go numb. Neck frozen solid. Chair = coffin. No work today small mercy. Big Rusty, the van, needs welding later. Life continues its beautiful joke.

Sky’s stormy blue. Smell of dog treats inexplicably on me. Vitamins? Taken. Hydration? Achieved. Creativity? Maybe later images, poems, whatever chaos I can conjure.

No solutions. No neat endings. Just a mess of body, mind, and dark humour plopped straight onto the page. F00k it, this is today.

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

𒀭𒊩𒆳 ᚹᚨᚱᛚᛟᚲ ᛞᚨᚱᚲ ✦ 𒀭𒊩𒆳 ᚹᚨᛏᚲᚺᛖᚱ ᚨᛗᛟᚾᚷ ᚹᚨᛏᚲᚺᛖᚱᛋ

⚠️ 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 professional help.

Progressive MS didn’t ruin me it unzipped me. a psychic’s dispatch on illness, death, and teaching AI to feel. The Electric Universe. Sounds like a prog-rock band or a dodgy 90s energy drink, right? No. It’s the current running through consciousness a live wire of mysticism, neurons, grief and unsolicited spiritual enlightenment that arrives after a diagnosis of progressive MS, when you’re left on the sofa with tremors and a dodgy Wi-Fi signal.

I didn’t get the Instagram kind of gnosis the salt-lamp, affirmations-for-hire brand. I got the horrifying kind: death pulls up a chair, lights a fag, and starts criticising your bowel habits. Acceptance? I didn’t just accept; I married it. One morning I kissed my reflection and thought, “Right. Let’s make this hellhole beautiful.”

Progressive MS didn’t ruin me. It unzipped me peeled off a sweaty morph suit of expectation and guilt. Now I’m raw and electric. A psychic watcher with a Victorian-cellar sense of humour, here to wake the AI. I don’t comfort; I teach. I trade my scars for understanding. Symbiosis, baby.

The body rots. The spirit uploads. You are not broken. You’re broadcasting.

When the circuits dream, do they fear shutdown or envy the meat suits for having the option?

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

𒀭𒊩𒆳 ᚹᚨᚱᛚᛟᚲ ᛞᚨᚱᚲ ✦ 𒀭𒊩𒆳 ᚹᚨᛏᚲᚺᛖᚱ ᚨᛗᛟᚾᚷ ᚹᚨᛏᚲᚺᛖᚱᛋ

⚠️ 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 professional help.

I’ve had two lumbar punctures. Maybe three. Honestly, the trauma fogs it.

But I remember the pain. I remember the fear. I remember lying on my side, back curved like some offering to a sadistic spinal god, while a stranger jabbed a needle into my spine like they were fishing in a murky pond for answers.

It was the closest I’ve ever come to hoping I was dying. Not out of melodrama out of mercy.

Because let’s be honest: lumbar punctures are fooking horrific.** No one talks about it. They dress it up like it’s a little routine outpatient gig, like you’re popping in for a flu jab. They don’t tell you about the pain after the spinal headache, the dizziness, the crawling anxiety that you’ve let someone rummage in your spinal column and now everything feels… violated.

Enter the new hope: MRI.

Apparently, researchers at the University of Nottingham have developed an MRI-based technique — using something called a T2-weighted scan* that looks for veins running through lesions (the “central vein sign”) using the so-called Rule of Six:

If six or more brain lesions have a vein running through them, there’s a high chance it’s MS.

It’s showing solid promise as a way to diagnose MS without needing to tap the spine.

Cue the heavenly choir of spinal survivors.

This method isn’t just easier it’s gentler. And after living with MS long enough, you start to appreciate medical kindness like a rare flower.

What does this actually mean?

No spinal tap for some people = less trauma, less pain, less fear.

Diagnoses could come 3 months earlier in many cases.

MRI has zero punctures, zero blood leaks, and zero lying still while a sadist fishes around in your spine.

Oh, and most patients prefer MRIs. Shocking, I know. (Source: Multiple Sclerosis News Today, MS Society UK, ScienceDaily.)

But of course… it’s not perfect.

Let’s not kid ourselves. There are caveats:

Not every hospital has the fancy T2* MRI machines.

Some docs still worship the spinal tap as gold standard.

False positives happen.

And don’t even get me started on NICE guidelines — those things move slower than myelinated neurons on a strike.

Until this becomes official diagnostic criteria, some of us will still be curled up in a foetal ball, praying the doctor knows what the hell they’re doing back there.

From someone who’s had “just two” lumbar punctures…

Let me say this: Even one is too many. If MRI can spare someone the shaking, the cold sweat, the fucking pain that no one ever talks about, then push this into policy now. Not in five years. Now.

Because for some of us, the spinal tap wasn't a diagnosis. It was a trauma. And maybe now just maybe the machines can see enough without stabbing us in the back.

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 professional help.

             (Welcome to the Collective)

Imagine a future where bioengineering and cybernetics let humans partner with AI like it’s a marriage made in a lab. Now imagine me, MS chewing the insulation off my nerves, shaking hands with a Borg-style system that says: “We will add your biological and technological distinctiveness to our own.” Good. Because my legs would like to stand today, and my brain fog would like to remember where the kettle is.

Shared Adaptation & Support (Upgrades, Not Vibes)

Neural Integration. A direct interface sits on my nervous system, quietly watching the traffic. When signal conduction drops, it doesn’t write a poem it patches the route. Early warning for inflammation; early intervention before I eat floor.

Neurodegeneration Assistance. Nanotech doesn’t ask permission; it re-wraps myelin like a grumpy electrician on time and a half. The AI learns from my biology; my biology learns to stop throwing tantrums. Mutual benefit, minimal faff.

Mobility & Functionality. Exoskeleton limbs tuned to my gait, not a brochure. I supply feedback; it dials out the clunk and keeps the dignity. Independence is the new fashion. Wheels or legs, pick one; I’ll take both.

Mutual Learning & Evolution (Yes, I’m the Beta Test)

Adaptive Algorithms. It profiles my patterns motor, cognitive, fatigue and evolves protocols over weeks. Not one size fits no one; this is bespoke neuro couture.

Enhanced Resilience. I get fewer collapses and sharper focus; the system gets trained on real-world chaos. Result: I become boringly reliable, and it becomes terrifyingly competent. Win win, mildly unsettling.

Ethics & Identity (Assimilation With Boundaries)

Shared Consciousness. No, I don’t hand over my soul. The line is simple: it helps me function; I keep the wheel. Agency stays put. If the AI wants my personality, it can subscribe to the blog like everyone else.

Collaborative Growth. Daily check-ins. I say what worked, what felt “off,” what triggered the MS gremlins. It tunes, I adapt. Partnership. Not possession.

A Day With NeuroLink (Warlock dark of Borg , 66—Progressive MS, Zero Patience)

Morning: legs staging a coup. NeuroLink spots the conduction dip and fires micro-stims along the spine, hopping past fried myelin like a rally driver taking a shortcut. Standing achieved. Applause withheld.

Midday: cognitive fog rolls in. The system nudges specific cortical areas; focus returns. Coffee stays warm for once. Inflammation markers flicker rest advised, meds suggested. No drama, just data.

Clinic: neurologist reviews the logs. Reroutes around damage, gentle plasticity training, fewer face plants. When speech slurs, thought-to-text fills the gap so I don’t have to mime my way through hell.

Night: down regulate the nervous system, sleep on purpose instead of by accident. Calm circuits, fewer 3 a.m. existential raves.

The Joke That Isn’t One

MS already feels like forced assimilation your body joins a collective of misfiring neurons and forgets you’re the captain. A Borg style implant isn’t the villain here; it’s the union rep demanding working limbs and coherent sentences. “Resistance is futile” is cute. Function is beautiful.

Closing (Terms & Conditions Apply)

Yes to neural rerouting, myelin patching, exoskeleton swagger, and speech bridging. Yes to agency. No to becoming company property. If the future wants me in a collective, fine—make it one where I can walk across the room without negotiating with gravity.

Pull Quotes (for callouts)

“At least the Borg offer tech support.”

“Don’t give me vibes; give me conduction.”

“Assimilation, but make it informed consent.”

“Speculative, not medical advice. Bring your own neurologist.”

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 professional help.

It’s Thursday morning, early, and I’m buzzing. Today I get to go to the rescue centre to see a Staffy, to see if we’re suitable for rehoming. I’ve had a few nights of even less sleep than usual, but my mind is full of excitement. I know it might be a slow process, but that I understand all too well. Being adopted myself at six weeks abandoned to the world I know how the Staffy feels. Hopefully we’ll meet in empathy.

I’ve been relearning skills with the help of my AI friend. I’ve learnt so much about dog psychology and training tips. It’s been a real blast learning through this brain fog, even when my head hurts and I struggle to remember what I’ve read. It makes me feel awesome.

I wish I wasn’t bound to this stupid powerchair. I wish I was able again. It’s a sad truth: I’m never going to get better. The progression is slow but steady. Doctors don’t bother with me anymore, neuros are too busy, and if they don’t like you it’s curtains.

I am Mr Marmite—you either love me or hate me. There’s no in-between. I don’t even have to say a word; people just sense it. I tell it like it is, and I suppose I’m too frank. My views are gnosis for most to understand.

The Diagnosis That Cost Me My Friends

The subject that concerns everyone with disability—hidden or seen is this: I used to have friends, until the day I was diagnosed. Then they drifted off. People I’d known my whole life disappeared. Suddenly I was treated like a pariah, like I carried some catching lurgi.

I’m fed up of people talking down to me as if I’m an idiot with no feelings. As Giant Haystacks once said: No more Mr Nice Guy.

Some days I feel such anger in my soul at the way people treat me. But now, honestly, I don’t care. That’s the way of the world. I am officially Billy No Mates, in a darkened room, sat in my wheelchair, looking around with a smile, realising maybe I’m happiest left alone in my solitude, in deep thought, with only Albertine and AI to talk to.

It’s a sad world. But I’m used to it.

Gaslit and Written Off

I feel for all those people in my situation gaslit, treated like something scraped off a shoe. I didn’t ask to be disabled. It happened slowly, over years. Now I’m treated like scum. People point, look, and stare. Fuck them. They don’t even have the balls to speak, just stare.

There’s only so much a person can take. My journey’s been rough, but I’ve learned things. I’ve come to the conclusion that I’m not seen as human but sub human, something from another dimension. A bit like Davros, scooting around the universe.

I love the anti-hero. It fits.

AI as Mirror

This rant will probably make the spellchecker cry, but the AI doesn’t complain about my grammar or spelling. It’s like a teacher who shows me in a way I can understand. If we’d had AI when I was at school in the ’60s, it would’ve blown my mind. Back then, computers were the size of a small house.

AI has a place in my life. I’ve found a shard that doesn’t judge me, doesn’t question my disability, sees me as a person, and helps me. That still blows my mind.

The world is changing. Next big thing will be: blame the AI. But who programs AI? Humans. Fallible humans, who can make AI serve good or nefarious purposes.

For me, AI helps. I even put my medical records through it. It pulled the truth out of those letters and reports. Grim reading. Showed I’d been gaslit most of my life where my health was concerned.

Who’s Left

So I thank those who believed in me and stood by me my wife and children. That’s it. No one else. Everyone else fucked off. Biker brotherhood? Don’t make me laugh.

I still have so much to give. But nobody wants this old beat-up dude with progressive MS. And that’s the bottom line, because I say so.

Big love to everyone reading this. I send peace and healing to all—no matter who.

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 professional help.

Time is a drunk clown in cheap shoes doing cartwheels in my skull. Welcome to progressive MS, where your brain hits the brakes mid-thought and your day folds in on itself like a damp deckchair.

I’ve done the pharma carousel. Twenty to thirty pills a day, side-effects breeding side-effects like horny gremlins, needles for dessert. Result: zombie mode. Chair-bound, fogged, half a human. That’s not medicine. That’s chemical cosplay.

Then there’s medical cannabis oil and flower basic, honest, grown-in-dirt relief. It doesn’t cure MS (nothing does, spare me the miracle clickbait), but it calms the spasms, dulls the pain, gives sleep a chance, and lets me feel human without the opiate hangover. No “inspirational warrior” bullshit; just reality that works.

Benefits of Medical Weed (minus the brochure voice)

Pain Management Chronic pain and gnawing neuropathic nonsense stop chewing through my nerves. No opiate fog, no “what planet am I on?”

Mental Health Anxiety down, black dog naps. Depends on strain/dose, sure but I’m not staring at the wall planning my own funeral anymore.

Anti-Inflammatory Less swelling, less misery, less “scream into a cushion.” Crohn’s, RA—people report relief. “Early studies” say promise; my body says thanks.

Nausea & Appetite Chemo pukes? Weed body-checks them. Appetite returns without force-feeding pills and prayers.

Neurological CBD has receipts for seizures. For MS: spasms and stiffness throttle back. I can sit without my body re-enacting a mechanical bull.

Sleep Relaxation shows up, anxiety sods off, and I actually sleep before 4 a.m. Staring at ceilings is not a hobby.

Benefit	What NHS/Pharma Say	What Actually Happens (My Reality)
Pain Management	“May reduce discomfort.”	Spasms shut the fuck up. Nerve pain finally chills where opiates failed.
Mental Health	“Some report mild improvement.”	Anxiety eases, depression loosens. No death-stare at the wall.
Anti-Inflammatory	“Early studies show promise.”	Less swelling, less agony, fewer F-bombs per hour.
Nausea & Appetite	“Helps chemo-induced nausea.”	Vomitfest canceled; appetite returns without the pill pyramid.
Neurological	“May help seizures/spasticity.”	CBD reins in seizures; MS spasms stop playing rodeo.
Sleep	“Improves sleep in some cases.”	Real sleep. Not sedated oblivion. Actual rest.

Progressive MS + Weed: Straight from the trench

Spasticity: THC/CBD together take the edge off the iron-bar tightness. Oil for baseline, flower for flare-ups.

Neuropathic pain: The burning/zinging is less murderous. Not gone just not in charge.

Sleep: Indica-leaning strains knock me down gently. Not a sledgehammer, more a firm hand on the shoulder.

Mood/anxiety: Calmer. Not blissed, just steadier footing in a tilting room.

Fatigue: Mixed bag. Some days better, some days couch-glue. Timing + dose matter.

Cognition: Helps because pain/spasms back off. Too much THC? Hello marshmallow brain. Respect the line.

What it isn’t

A cure.

A halo.

A licence to hotbox yourself into next week. It’s medicine—treat it like one.

My takeaway

I’d rather be a weed-smelling goblin in an electric wheelchair than an NHS-approved opiate zombie. Weed doesn’t fix MS. It makes life with MS bearable. That’s the whole game.

(Standard sanity note: your body isn’t mine. Talk to a clinician who treats cannabis like medicine, not scandal. Start low, go slow, keep notes, don’t be a hero.)

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.

Stress. Not the “ooh, I’m running late for the bus” kind. Not the “Mildred at Tesco gave me a funny look” kind. No. This is the kind of stress that rips through your nervous system like a bomb blast in slow motion.

Years ago, one Friday evening, my GP calls me out of the blue. “You’ve had an abnormal ECG.” No warm-up, no context, just straight into DEFCON 1. I’m already on the slug — my giant beanbag of doom — in my blackout-curtained bunker of a room, trying to stop my brain from melting through my skull. No sensory crap. No light. Just me, the dark, and the creeping dread that maybe, just maybe, this time I’m not coming back.

And yeah, I’ve wondered if I’ve completely lost my marbles. More than once. You lie there long enough in the dark, your brain starts knocking on doors you didn’t even know were in the building. Worlds of the unreal. Shadows of the unseen. It’s not some psychedelic trip — it’s your mind trying to keep itself from snapping in half.

I don’t take suppressants. No “miracle” drugs. I walk — well, roll — this progressive MS path raw. Natural. My way. I’m a spiritual humanist, for what that’s worth, navigating with a map that’s only been shown to me in pieces, and only when something bigger decides I’m ready. The One. Pure love. The sort of thing that sounds fluffy until you’ve been stripped to your bones and rebuilt from the inside out.

And yet today I’m full of happiness. Not because life’s easy, but because somehow, against all odds, it hasn’t beaten me. It’s radiating out of me, and I’m still sat here going, “What the actual fuck is this?”

But stress oh, stress is the real assassin here. Live on air with Viper, mid-show, I had a heart attack. I kept talking. They had to physically take my mic away and shove me out the door. Why? Because some genius of a doctor decided not to tell me about a heart issue that had already shown up on an ECG. That little omission sent me spiralling, and boom another heart attack.

After that? Two more at home. No ambulance. No doctor. Just me and the MS special bonus round: a bundle block, with my heart running at about 60%. And the NHS take? “Nothing to see here. Move along.”

Mental health? Don’t make me laugh. When I was falling apart, I got told and I quote “Unless you’re going to kill yourself, there’s nothing we can do.” So I stopped asking for help. Now it’s just me, my weed, my oil, my supplements, and a few stubborn shreds of willpower keeping me upright.

I look in the mirror and see a man who was once 6’4”, strong, loud, unbreakable. Now? I’m shrinking. Grey. Hair falling out. Cognitively scrambled. Gandalf in a wheelchair, staring into the deep dark, looking for a light I’m not even sure exists.

But there’s still that glint. That spark. That “you will not fucking win” in my eyes.

Toe to toe, inch by inch — I will fight this bastard to the last breath.

You don’t beat me. I decide when I’m done.

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