Overwhelmed. TMI’d up to the hilt. My Mind has been blown to pieces… and then those pieces have been blown up too.
I can’t even… You know, I am buzzing on the inside… I mean literally, like every cell has its own TENS machine or Thumper Wand.
Too much everything. There’s no time to think. No time to wind down. There’s no time to Sleep – and they come with Nightmares anyways.
I’m blacking out – because All of This is just Too Damned Much. I am dying inside. I don’t want to know about any of this. The Pain is Ridiculous. The Emotional Turmoil is Overwhelming and Pathetic.
I need Space. Headspace. Peace – from the Chaos, the noise, the constant haranguing. Something always has to be done. Or noted. Or talked about. There’s always a Ping. There is always someone talking. Then there’s people walking in and out of my room, as they please, talking about stuff they could message me with.
Things keep happening and going very, very wrong… A continuous chaotic cacophony of Mind-Blowing, Brain-Breaking Stress, that just seems to never, ever end…
Nothing goes right. Nothing goes easy. Nothing I do is *enough. And worse of all, is that I can’t stop other people from messing with my head, giving meMeltdowns, frightening me, Badly Shocking me, or breaking The Rules and Harming Me… Destructive, Harmful, Destroying.
I haven’t stopped. I’ve been going, going, going, and haven’t even barely taken a breath for myself… Everything takes time away from me. There is no rest. There is no peace to steal. There is no respite. There is no Mercy…
The Agony… The abundance of TMI… It has me blacking out into hallucinating unconsciousness; one that is uncomfortable and frightening.
Physically, I can’t move. Breathing is difficult. I am “imprisoned” in my Room again. I am Resentful, Frustrated, Hateful, Forced into this…The Agony is Unbearable.
These Feels are… Heavy… And I don’t like them. I only want them to go away.
I went to physio. I wish I hadn’t. Even though it was technically a “good session” — productive, challenging, effective… It was not a good experience.
Mainly, I’m upset because after all my (emotional/ psychological/ mental) hard work, I’ve been thrown back to feeling inadequate, clunky, awkward. It was horrible, making me feel like physically vomiting; the nausea siting in the bottom of my throat like a boulder. I felt shame, resentment, disgust (with myself, and also the physio). And the worst thing—My chair no longer felt like an extension my myself, like it usually did now.
This was how I felt for years. When my legs were failing, and after they failed. When I had to learn to deal with spending my moving life with a wheelchair. Learning to realise, that — amazingly — I was not “confined” to a wheelchair at all, as people so often expressed. No—The exact opposite, in fact. I was freed by my chair!
The realisation was slow coming, but it was astounding. No longer was there suffering of pain through my hips and back, wobbling on my feet and afraid I would fall. Over time, I became stronger, and then when I also had Neuro-Physio with the previous physio specialist, who was amazing, I got even better. Even stronger. First with Musty (GTM Mustang) and then with Kushty (Küschall K-Series), I become better, more capable, more confident, more accepting. My lovely chairs helped be better, stronger. It becomes my new normal.
Then someone turns up and says… it’s not. Not normal. Not good enough. Not something to be confident about.
As good as physio might be, the new person is not. She’s not like the last one. She hurts my insides, my Feels. Today, she kept going on about using my legs, “waking them up” and maybe walking. “Ooooohhhhhh, you never knowwww…”etc, etc, hollow, disingenuous, delusional idiotic bullcrap, over and over and over again. Seriously, she must have said exactly that five or six times. At least.
It felt like the obvious underlying statement was, only that was good enough—having legs. That I should blindly hold out all and any fragments of hope, and everything short of that was insinuated to be —gods-damned presumed to be! — nothing but a pathetic and miserable existence.
This ridiculous notion is what they call “Hope” — but what it really is, is Magical Thinking. And it just makes my heart and soul dissolve and freeze into dark black ice, caught between utter hopelessness and fuming anger and insult, at such horrendous ignorance.
What I prefer is realistic expectations, not stupid “oh, you never know…” utter bullcrap. I could say the same thing about walking on the moon, for gods-and-spirits’ sake! “You never know…!” Gah! It’s moronic, babyish, and, frankly, pathetic.
Oh, and believe me when I say I couldn’t care less if it’s “coming from a good place“, or they mean something nice. If you mean something nice, say something… y’know…Nice..?! Intention means nothing if the result is nothing but harm.
I will never understand the NTs’ obsessive insistence of clinging to blind, delusional “optimism” (aka: Magical Thinking). What’s wrong with Truth? What’s wrong with Reality? What is wrong with being less than Fairy-Tale Perfect…?? 🤬😡😤
I understand “Never say Never” about Unknown Quantity or Unknown Outcomes, especially with people. I fully accept there could be some connective electrical activity re-triggered and re-awakened after the (stress-induced) traumas I have endured over and over again. Unlikely as it is. But there are many, many better ways of communicating this, including offering great support (this is what her predecessor did). Pity is never an answer.
No scientist or mathematician got anywhere by basing their answer (or presumption) on nothing but a premise or hypothesis — Yes, almost anything is technically possible. But then, there’s also Magical Thinking, which involves utter Unicorns-and-Rainbows levels of nothing but fantasy.
Scientists allow for anomalies and possibilities, and yet they also don’t expect the moon to fall down to just 33,000ft above sea-level so we can all have it easy and just fly there on a 747 widebody, or for a black hole to morph into a sandwich, because “it’d be cool”. 🤨🤨🤨
In other words, we can’t just manifest crap because we prefer it.
If that was the case, I’d be using my own 3 wishes to make my natural hair to that of Disney’s The Little Mermaid, for my legs to be her tail, and for the ability to read people’s minds. I would not be wasting one on whether I could walk again…! 😒🤨😤
I cannot even begin to explain how these sweeping statements put my teeth on edge. Disingenuous. Despicable. Fantastical. Delusional. Weak. All things I am not, and refuse to be..
Maybe it’s the ASD. Maybe it’s just (or/and) Alexithymia. But all of that delusional stuff just… Sends me into a tailspin. I’m here, I’m *Me*, and *I. Can’t. Walk*. I have a pretty chair with cool wheels to make up for it, and the physical strength to help me function and manage it. There’s nothing wrong with that. Is there…?
What I *do not* have is Mental Strength, and I’m Traumatised and Fragile. I cannot bear being told that basically I should do nothing but “hope” I can walk “one day”, because nothing else is good enough, and anything else is entirely… Pitiable.
So… What, then? I genuinely do not understand… Why is it so not OK to be like this, like me, that I’m being pitied and told to invest in false hope by a physiotherapist? One who dismissed what small (or huge, to me…) progress I had made, in favour of sweeping statements of disingenuous pity and false hope?
Am I supposed to twiddle my thumbs in the Lobby of Life, waiting for the 0.000000000001% chance I *may* feel or move my legs again? I have a better chance of winning the lottery… and I never play it. Am I now just some-thing… That I’m not worthy to do anything else, I I have no use of my legs? Am I just to sit around and be Pitied? Is that supposed to be it, now? That “walking should be the bee-all-and-end-all of life and everything” is… life-limiting. Debilitating. Disabling.
To me, it’s a rediculous notion for anyone to have… And for it to be utterly despicable in a damned physiotherapist.
I’ve spent a long time trying to build up to having confidence in being in a chair. This made it all come crashing down. Swept away, destroyed, what little confidence I had started to develop in myself as an active wheelchair user. I cried — and I do not cry easily, if ever. I’d worked so hard to feel some self-worth in being a wheelchair user and physically incapable. Now, it was gone.
I do not wish to sit in Limbo, waiting for some fantasy “Maybe” (which isn’t real at all). I’m not putting things on hold anymore — I’ve been pushing myself to go ahead and be Me, which includes having Wheels and getting on with things. Even if its small things.
I don’t know if I have the… verbal sophistication?… to fully explain what I mean. Why it hurts, damages, so much. Nothing I’ve written here, or could write, could convey, that is accurate to how much this affects me and hurts me. Harms me.
I feel Depression inside, with its special brand of Extreme Anxiety & Sad. They’re playing their part well, and strongly. Inflicting their “Bad Feels” upon me, and more than occasionally drowning me in them. Making all these things worse, communication and processing longer. Meaning this “incident” with the physio made everything 10,000 times worse.
It’s all become a bigger mess now. This has been added to my brain as yet ONE MORE TRAUMA to deal with. It shouldn’t be like this.
There really is only so much that a person can take… and I passed my limit a long time ago.
Anxiety and Chaos rules my mind. It feels like it’s been long buried under mountains of agonising pain, sorrow, grief. Fibro-Fog, medication, and more and more Chaos and Anxiety. I can feel my mind still there, calling, struggling to be freed, to be heard… yet, there seems to be so little I can do about digging it back out.
As long and all this overwhelming Anxiety and Chaos rules me, rules my life, is forced upon me – truly, it seems that no matter what I do to prepare against it, it floods and breaks through my defences and laying siege until I can do nothing more against it. – it will Rule me. It overwhelms me. Then, it eventually takes over me. My life. And now, it just simply continues to do so… because I have only so many spoons at all, and that number is barely above Zero, and none of those spoons are even remotely strong enough to fight against the sheer mountain of things that continue to suffocate me every minute of Every. Single. Day.
With no Short Term Memory to speak of, and pretty much no Long Term Memory to fall back on (although, thankfully, the odd one can be brought out with certain triggers, unfortunately few and far between), it’s like I am nothing and no one.
As an Aspie, who once remembered everything and anything just about, this fact is near killing me inside. I still don’t know what to do with it – the grief and frustration of going through this, being forced to live without something embedded into me, that was an intricate part of me… Quite often, it is all too overwhelming. Even the inability to control my environment was entirely reliant on this… and without it, Anxiety and Chaos reign entirely. It is painful and frightening, and there seems to be nothing I can do about it – and I feel this because I have gone through everything I can think of over these past Five Years this has been happening to me…
I physically cannot move – my condition leaves me with only the shoulders and arms and what is above it; pretty much nothing else is movable by my own conscious will. I must remain on the floor whilst upstairs because my chair (or any chair) cannot fit up here; the house is too old and the landing is far too narrow to accommodate one. This means that I remain next to useless up here – unable to move or control my own environment in my bedroom. Despite assistance, there is no way to keep it sane without someone perfectly able-bodied to take things out and put them away as required. Whilst I may be able to retrieve something, putting it back may cost too much spoons, or be too difficult – or worse, I might forget.
I have been numbed by the sheer and exhaustive amount of confusing and destructive emotions that keep washing over and drowning me. I do not like emotions – actually, I loathe them, and wish they did not exist. And, quite frankly, there are definitelyfar to many of them. It’s a cornucopia of horror that I flail at, until I fall victim to my terror and end up falling and drowning beneath them all. “NT” people have called this dead numbness “depression” – but I’ve studied psychology for years, and what I have has never quite been fully described by that theory, and it does not fully cover what it is that I experience.
I am TMI (Too Much [Sensory] Information) when it comes to all these emotions – and all are fuelled by my two arch enemies: Anxiety and Chaos. I literally cannot live like this – I barely even exist like this. To live, to participate in… well, something, anything… to do what I love again… That would be Everything.
So, by that measure, it seems that right now I would have nothing…?
It’s New Year’s Eve. The end of 2017… And I’m definitely glad to see it go. This last year has been the year from Hell itself.
It started with agony that could not be compared. With my starting to lose the ability to walk at all. With my losing the ability to crawl up the stairs. With my losing the last few threads of what was left of me.
2017 was the year I stopped being able to walk. To use my legs. It was the year I had to get a stair lift. The year I had to get a “real” and “proper” active wheelchair – something that caused a lot of pain, difficulty, complications, and tears. The year I found out I had been suffering an elusive condition for the last 19 years and it had impacted greatly upon my Fibromyalgia – something no one had ever heard of, called Hemiplegic Migraine… and I found that out on what should have been my late grandfather’s birthday.
This was the year my best friend left for South America, and was no longer here. This was the year I went completely numb and unable to feel anything touching my skin or pain from the outside. This was the year I could no longer stand for a shower or get into the bath. The year where gaming became more and more elusive because my hands and focus no longer worked properly. The year Fatigue came to over-run and ruin my life. The year PIP decided to decieve and scheme and refuse to even acknowledge the difficulties I have by outrightly lying about me in their reports. The year I was betrayed by my own therapist, just the third time we had met, and after waiting over a year on the waiting list to see her in the first place.
This was the year I learned you can lose your life without ever having to actually die.
I started 2017 with the ability to shuffle with walking aids and go for a shower… And I am ending it without the ability to walk or properly move my legs, wearing a catheter, permenently in a wheelchair, unable to go to the shower or get into the bath, barely able to leave my room, struggling to move and sometimes even breathe.
2017 was the year I think I truly died inside.
It started with hardship and loss. Went on to destroy what was left of me and my body. Ended with trauma and being near-bedridden.
On the bright side, I also ended up getting 2 graphic card upgrades and end the year with the GTX 1070 8GB OC. I was also introduced to several amazing games – in 4K High/Ultra, too – and got a Lenovo YogaBook – which is terribly fun to have.
And I got to see The Last Jedi… So at last one good thing happened.
I really hate these flare-ups… Is it just Fibro, or is it more? I’m just so exhausted I can’t think straight, or even at all, anymore. It makes me so ridiculously ill, so tired and drained, so unable to do anything, not function at all.
I am lost inside it. Numb and dead inside with nothing more to give.
Drained Fatigue. Exhaustion beyond all comprehension. Exacerbated paraesthesia or neuropathy. “Buzzing”. “Paraesthesia pain”. Severe internal temperature fluctuations, like when one has severe fever or flu. Bad Palpitations. Severe Nausea. Blackouts. Inability to wake up.
Emotional fear. Scattered mind and thoughts. Inability to comprehend even basic things. Even less capability to remember things. No focus at all. Unable to do just about anything. Left with vacantly watching rubbish on TV because can’t focus. High Distress. Depression. Severe Hyper-Anxiety. Terrified – of everything. Overwhelmed. Barely able to move. Unable to function.
All I do are the basics. Less than the basics. And yet this is still what I have to live with – that and so much more. It doesn’t seem to matter that I try and do as little as possible… I still end up feeling so awful, so drained, in pain. If I try and do more than nothing, then this… thing… punishes me relentlessly, by making everything so much worse.
This makes it so completely horrible, unmanageable, un-livable. I am unable to do anything I want to, and that’s not because I’m in so much pain or can’t walk. It’s because I am so very too exhausted to do anything. There are things that can be done to control pain, Fibro… well, to a certain extent, anyway… but there seems to be nothing to combat inexplicable and extreme exhaustion that’s so bad it makes you pass out. Might not be too surprising that coffee is barely of any use whatsoever, either. So there’s nothing at all to combat it. You really do just “have to take it”. Without a single antidote to be had to help at all.
Sleep does nothing. “Rest” does nothing. How can you even “rest” when everything all around you confuses and terrifies you? When you’re so anxious, so distorted, so “zoned out”, so unable to function whatsoever… how can you really “rest”? It’s like I’ve got a broken health bar… or one from Dragon Age: Inquisition… It just doesn’t regenerate at all. And I’ve got no potions to bring it back either.
Taking me out of the game, for as long as its there. Or maybe, quite possibly, for good.
Storm Stella… Thank you for being yet another terrible import from America. For the last week or so you have been driving every nerve and cell in my entire being utterly bananas, and I’m in constant paraesthesia pain – I may as well be attached to Ol’ Sparky for the amount of electric shocks, buzzing tingles and burning, like sunburn, that I am currently having to ensure.
So thanks, ridiculously horrible storm that came from across the sea to cause so much misery.
It was supposed to be a good week this week, and especially today (it’s the release of Mass Effect: Andromeda [game]). But all this has made it impossible to manage to be anything close to even “Meh”. Definitely not “OK”.
It’s beyond trying, being dictated to by not only this condition but also the bloody weather. It’s even messing with my von Willebrand’s – and I have no idea how that happens. I’m already restricted by the damn condition, I really don’t need any more trouble because the atmospheric pressure has gone ga-ga…
I’ve been knocked off my feet and trying very hard to be Que Sera about it all… but this comes on the tail of a stressful couple of weeks, including being ill with flu for about two weeks as well. Then just as I was starting to get better, Stella came… and now I’ve got yet another flare-up from Hell again.
I’m keeping it from getting too much worse with the essential oil blend and Magnesium Oil. But there’s only so much even they can do in this situation. The paraesthesia has gone mad and there seems to be no stopping all those damn horrible symptoms that comes with it.
I was hoping that things would be back to normal by now. I wanted to play Mass Effect: Andromeda on Day One and enjoy it. I wanted to make it to an appointment to help teach someone about basic tech skills tomorrow. But no. It’s not happening. Instead I get self-consciousness, zombie-ness (and I’m not even Walking Dead… more Sitting Down Whilst I Rest Dead…), terrible sensations of being burnt and electrocuted, my hands don’t work properly (typing this is a nightmare for my fingers, but longhand is even worse), and I’m not sure how on earth I’m going to be able to focus on my new game and the lovely Collector’s Edition Guide to go with it. And I’ve been looking forward to this for years.
I am exhausted… so much so it’s more akin to being drugged with drowsy pills, which is really not easy to handle. It often makes my grumpy and without patience. I’m trying, but I don’t know how long it will take before I can’t take it anymore and snap… although I obviously hope I do not. I did not get any sleep last night because this morning there was going to be no one here to help me take my medication, and because of the weather I knew I wasn’t going to manage it alone if I had slept, so I stayed up the entire night to ensure I took it properly and on time. Afterwards, I passed out in my Aspie tent for about 2 hours, then I was up again. I was hoping to play my game. Despite it being there, in front of me, after my father brought up the packages that had come in the post (when he finally returned and I was cat-napping), I had to be disappointed in realising I wasn’t anywhere near up to doing much of everything, as the exhaustion and paraesthesia pain and intense sensations caused by the air pressure once again created an existence I could barely even exist in. Let alone play my new game.
It’s one thing when you’re in control of your health, your recovery or stability of your condition… but when something comes along and can dictate so absolutely what happens to you and inflict so much upon you, it’s hard to process that. It’s impossible to manage to control it. You can’t “get over it” or undo it, and the likelihood is that – after the awful and super-debilitating flare-up is finally done with half-killing you – you are then left to deal with the aftermath and recovery from it.
The constant storms of 2015/16 were so constant, it’s taken me nearly 10 months to start a true recovery (of sorts, relatively speaking) from it… then just when I think it’s safe to go back into the water … always something like this happens. Illness, weather, air pressure… something always seems to turn up. The bottom line it that you feel like you’re simply never in control of your life, condition, or health, and so end up feeling so hopeless and despondent.
It’s also the last thing you need when you’ve got an ASD brain… The random inconsistency, the lack of control, never able to plan anything, and everything constantly in flux even minute to minute, let alone any longer… It’s all a nightmare that never ends, and the only thing possible is learn how to live like that. Somehow find some consistency in non-consistency and non-complacence in how your condition or “triggers” behaves.
The only thing I can think of to cope with all this now (and it’s taken long enough), is to find a bunch of “safe” things that are always consistent despite the inconsistency in everything. More like “If-Then” kind of scenarios, and enough of them to cover as many eventual possibilities as possible – then there’s a constant stream of consistencies to find comfort and familiarity in – frankly, comfort and familiarity I simply used to get just by being in London (at home, my home). Because nothing makes much sense here at all, I need quite a few different “safe” things to have available, regardless of the situation.
Right now, all I want is for these symptoms to go away, my fickle concentration to return, to be at least almost entirely conscious, and to be able to play my game. I have a simple life with simple requirements these days… Something like that shouldn’t be too difficult to ask for – surely?
The more I am in this situation, the more it eludes and confounds me. It doesn’t help that it thus far has no definitive name. What really doesn’t help is the psychological aspect.
I checked around the Internet… There seems to be really little on ASD/ Autism/ Asperger Syndrome with neurological or physical chronic illnesses. There seems to be no precedent, nothing out there from other people who are or have been in a similar situation. There’s one or the other – but not both together.
I feel I am wondering out in the wilderness with no way of knowing which way to go, or where I am even going. There is so little help… Nothing but Waiting Lists, and then some. Lots and lots of them – Neurology, Occupational Therapy, Psychological Services… and then there’s more to come for diagnostics, physiotherapy, treatment, more appointments… A never-ending carousel of waiting. With no one to help in the meantime. Without a clue as to what might be wrong with you or why you’re suddenly like… this.
All I know is that it’s no longer Fibromyalgia. Last time I checked that required pain. Mine is all gone, replaced by horrible other things instead. No longer hyper-sensitive to cold, no longer in that pain I was in, no longer able to feel… well, almost anything. I’ve never hit my “funny bone” before and barely noticed. The dog can walk or bounce on me, chew [gently] on my arm and play with it. I don’t notice bumping into things, or people accidentally knocking into me, or things falling on me, or even touching my own arm or leg. I’ve been told there’s a terrible rash on my back and neck as a response to using oils – and I would be none the wiser if they hadn’t told me. I can’t feel it and it doesn’t even bother me. But when I touch it, it feels pretty rotten, I must admit…
Today my fingers went really numb… like someone had tied super-tight string at the bottom of each one; that feeling of the blood flow being cut off – and yet there was nothing on my hands at all. Not even gloves. I have also had a very hard time with extreme Fatigue (and I do presume I have a cold, to be honest), argued with gathering a Shard on Dragon Age: Inquisition, and my back and legs (especially my legs) have been quite “buzzing” and/or tingling (varying through the day). This morning I couldn’t even move or feel my own self to even try.
Right now I have to manage on the – rather genius and amazing – essential oil recipes for neuropathy and then for fatigue/brain focus, Devil’s Claw, Magnesium Oil (amazing), Neurozan vitamins, and coffee. Occasionally there’s minimal Co-Codramol (8mg/500mg) – almost always when I have a cold or infection – and Boots Botanics Ylang Ylang & Manderin “Aromatic Rollerball”. That’s on top of maxed-out Pregabalin pills. But without a definitive diagnosis, we’re all just pissing in the wind, guessing and hoping for the best.
I feel alone. Lonely. Because it really does seem I’m all by myself with this. Yes, people have neuropathic chronic illnesses, and yes, people have ASD. I am yet to find someone else out there who has experienced this and at least attempted to navigate this.
With the NHS in turmoil, and Social Care drastically underfunded, I’ve pretty much relegated myself to the Raggydoll pile. I just now wish to be the best I can be, especially psychologically. It’s a big ask, but it’s all I can focus on – and the only thing I can control now. There is just nothing left in my life I have any control over, and I have no idea. I am in the middle of it and I don’t understand any of this – so it’s hardly like you can expect anyone else to… But I do wish that at least I did. And this new numbness twist? That just hurts my head.
After three years and four months of enduring terrible pain, this condition suddenly and inexplicably changed. It was slow, but it felt like happened overnight nevertheless… it was gradual and I didn’t notice the severity of this constant change until it became a complete “180”.
Suddenly, it seemed like out of the blue the intense chronic aching pain I had endured so long vanished – changing entirely instead into numbness and the worse electrical pain I’d ever felt… Intense. Sharp. Unbearable.
It was suddently like I had been covered in “magic cream” and then hooked up to the worse TENS machine ever made. I can barely feel anything much on my skin other than the vague pressure of contact (maybe like through a thick wetsuit or something… but it does remind me of how having the Magic Cream felt). My right leg went almost completely dead, dragged and didn’t respond. My right arm also became quite weak and unmovable. I had to do things with my left hand again – which isn’t easy! – and the intensity of the tingling, prickling, buzzing, burning, electric shocks, numb-like pins & needles, and the most extraordiarily awful spasms that were all absolutely unbearable. Quite frankly, I wanted that pain back. At least that was vaguely treatable.
My mother went looking for alternative options, given I needed something that would work better than “conventional” treatment. I’ve always responded better to naturopathy – so essential oils for this was probably the answer… And thankfully it was.
I have found the following essential oils had beneficial properties that helped with neuropathic pain. Certainly with mine. This has been tweaked a few times, getting better and better (for me), and the results have been extremely positive – all things considered.
With this combination, I have fewer symptoms, and they’re down to “bearable” now. My right leg moves a little and my right arm works better. The numbness that comes from keeping my hands up for any period of time is reduced – particularly withe the Patchouli and Frankincense. I can even feel a little bit more on my skin.
Now none of it is “back to normal” or perfect by any means, but it’s better than it was. And when something is so unbarble you’re passing out, anything is better than that. To be able to have even a little more function in my right arm and leg is fantastic (a little is better than none, after all) and it also means
I will also be adding Basil x10 to it today, to see if it helps with the “brain fog” that comes with neuropathic conditions. I hope that it will help me to think more clearly, to be able to put down more short-term memories, to be more alert, focused, in charge of my own thoughts and decisions, to be able to use my mind again – even if, again, it’s only a little.
Over-enthusiastic Gamer, Goth, Geek, Techaholic, Dabbling Writer & Blogger, and Raging Coffeeholic ~
Loves Gadgets, Games, Tech... And Coffee. Lots and lots of coffee.
~ Obsessively-loving: Dragon Age Series, Mass Effect Triligy, The Witcher Games, Skyrim Special Edition, Elder Scrolls Online, Divinity: Original Sin Series (amongst others!) ~
~ Self-Built Gaming Rig: i7-4970K, 16GB RAM, 240GB SSD Boot, 1TB + 3TB HDD Storage, RTX 2080 8GB EVGA Super Black Gaphics, 1150 ASUS Z97-A ATX mobo, Windows 10 64-bit
... Oh, and did I mention I love coffee...?
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