I wonder how much Medical People truly care (like is it even 0.1%?) about what patientsā Lived Experiences actually DO to them⦠Physically, Cognitively, Emotionallyā¦? How the Ramifications of their ghosting and gaslighting and postponing and time-wasting have Very Real Consequencesto them, and the people around them?
Three MONTHS Iāve been waiting for my āURGENTā Suprapubic Catheter re-insertion. They did it in 7 WEEKS between Lockdowns & it was just before Xmas in 2020⦠and one shouldnāt need a WORLDWIDE PANDEMIC to actually have surgery they desperately needā¦.
And STILL theyāre not treating it for what it is⦠which is a ticking timebomb that will take me from being Severely Disabled as a Temporary Situation into One VERY Permanent One, where I am literally unable to manage ANYTHING for myself; not even turn over or sit up in bed, wasting away from Super-Fatigue, Mega-Agony, and spinning world that NEVER EVER seems to stop.
My 98yo grandmother could do More Than That, almost until the day she died. Iām Less than 45% of that age! My counterparts are working, raising children, going on trips or holidays⦠Iām just a year older than the Prince & Princess of Wales ā so thereās a VERY GLARING reminder of āWhat COULD have beenā right on the front pages of everywhere⦠My little sister is raising two young girls, with a mortgage on a cute 3-bed house, a job, going on said trips and holidays ā and ghosts me like I donāt exist.
Iāve now reached the point where I truly feel it wonāt take much more to put my body into Full Burnout & Severely Break Down Even More. The last time I was THIS ILL, I ended up with Sepsis and Septicaemia ā from Two Different Blood Poisonings.
⦠Call me deluded, but I REALLY donāt want to get on THAT crazy-train EVER AGAIN⦠So, Iām getting more than a bit freaked out about how badly Iām going downhill now, having to deal with the catastrophic fallout of dealing with the outcome of Full Incontinence.
MEGA-Extensive & Overwhelming Hyper-Fatigue alone has me now requiring the effect of 24/7 Care. Thatās BEFORE youāre talking about the Pain, Vertigo, Nausea, High Stress⦠etc.
Are you actually supposed to be able to GET Post-Malaiseā¦Thingy⦠from just breathing and existing? Cos I Do.
Anything more than that, even moving a little bit, and I am WRECKED, like Iāve done a half-marathon. Anything more than that, and itās worse than a Himalayan Treck to the peak of Kilimanjaro and back. I Am UTTERLY, TOTALLY DESTROYED ā for WEEKS. Maybe (usually) Months.
I have virtually NO Appetite, and barely eat, nor have any energy to manage anything, anyway ā a serious Sucker-Punch to the gut after spending the last TWENTY YEARS conning myself into eating to combat Anorexia. I SURE AS HELL AVOID DRINKING ANYTHING & EVERYTHING that I possibly can, even my beloved coffee ā which is just about destroying my soul, and definitely NOT helping with the Fatigue.
I donāt really sleep. Most of the time my body just runs through Functional Seizure BlackOuts ā itās ironically not conscious enough long enough to actually GO to āsleepā on most days. Other times, I might get maybe 2 hours of it, and it mostly happens by accident⦠I certainly canāt MAKE myself sleep (being Autistic, that was never going to be the case, anyway). Any I get makes me feel worse, or at least Just The Same (which is Diabolically Shite). I NEVER feel āawakeā ā not even āawake-ishā, which was my norm previously ā anymore.
Functional Neuropathic Disorder and Fibromyalgia Flareups are basically Permanent now, as a result of Force-Pushing my way through Almost IMPOSSIBLE Changes, which is the WORST thing one can do with these kinds of Chronic Illnesses. The Plethora of Crap that comes with that are all alive and well and WRECKING my Extremely Overwhelmed Body.
Iām at the level of Exhaustion where even JUST moving position of how I am sitting or lying down (as much as I can do) is enough to leave me spinning with Dizzy that makes me feel like Iām ON an Outrageous Alton Towers ride & fighting Overwhelming Nausea and Pain.
I am Forcing and Pushing my way through DEALING with EXTENSIVE & EXTREME AGONISING PAIN, Overwhelmingly MAJOR Hyper-Exhaustion, Brain-Melting levels of Vertigo & Nausea, and Immense Stress, whilst also feeling Extreme Anxiety, Distress and Frustration at having to GO through All Of This.
Itās also humiliating, dehumanising, demeaning, degrading, disgusting, sickening, and creates self-hatred like nothing else Iāve ever experienced before in my lifeā¦
Even Worse ā I CANNOT even change when I need to, or even HAVE TO. I physically CANāT MOVE or BE Moved ā the Spasms are too rock-solid. This is what happens when FND is triggered, particularly through stress, distress and high-anxiety.
These things are then made SO Much Worse by my Autistic Brain, with the distress and confinement have to this situation AND my body, with no end in sight and ZERO ability to Change It, which then sees the situation as threatening and frightening ā which causes no ends of Meltdowns and Shutdowns, in constant cycles, Because itās absolutely TERRIFYING, ā AND I am Utterly Damned Helpless to DO Anything about it, to Stop it from HARMING ME More.
⦠Itās not like Logic can dig me out of it, either ā IT IS Bat-Crap TERRIFYING to be SO Imprisoned inside my own self, in a body that is Very QUICKLY Degenerating & Shutting Down MORE & MORE from This.
Iām also haemorrhaging a small fortune in incontinence products to DEAL with this. Getting NO Help from Urology for THAT, either, naturally. These things are NOT Cheap and itās like BEING YOUR OWN DAMNED BABY. Worse ā Youāre Your Motherās Damned Baby, 44 YEARS LATER. Itās so utterly Degrading & Demeaning a situation to be in ā and one I SHOULDNāT even BE in.
Iām getting to the point where if my body doesnāt do it for me, Iāll end up doing it myself⦠I donāt want to ā BUT I do NOT want to be PERMENANTLY CONFINED to my body in the way that I am now.
IF this doesnāt Return To How It Was Before⦠And THIS IS my āNew Normalā⦠I think Iāll be seriously considering why my life IS worth living or continuing with anymore....