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Sock Knitter Porg

@sockknitterporg

RP Side Account: tiredapprenticesuri I knit socks. Disabled, spoonie, allistic, not NT. Gender issues, possibly female (she/her), 30, queer, Druid, white.
MINI UPDATE FOR AUGUST 24TH, 2021

I am updating a few things on my ko-fi / my spiritual blog -- the topics I'm currently covering the most are my experiences with spirituality and my experiences having a chronic illness (both journeys have been deeply spiritual + life changing).

My first official series started in August and will carry on into + throughout September since it's Sickle Cell Awareness Month. After finishing that I plan to write and transfer a few posts specifically about what sickle cell is and my struggles with it.

Today August 24th I will be rewording my bio, adding more commission slots in anticipation for the Fall, and I'll be adding a few cover photos."

✨✨ I accept paypal , ko-fi , and venmo is madamoliveI am currently seeing clients August 1st through December 31st ✨✨

There is in India a wild beast, powerful, daring, as big as the largest lion, of a red colour like cinnabar, shaggy like a dog, and in the language of India it is called Martichoras. Its face however is not that of a wild beast but of a man, and it has three rows of teeth set in its upper jaw and three in the lower; these are exceedingly sharp and larger than the fangs of a hound. Its ears also resemble a man’s, except that they are larger and shaggy; its eyes are blue-grey and they too are like a man’s, but its feet and claws, you must know, are those of a lion. To the end of its tail is attached the sting of a scorpion, and this might be over a cubit in length; and the tail has stings at intervals on either side. But the tip of the tail gives a fatal sting to anyone who encounters it, and death is immediate. If one pursues the beast it lets fly its stings, like arrows, sideways, and it can shoot a great distance; and when it discharges its stings straight ahead it bends its tail back; if however it shoots in a backward direction, as the Sacae do, then it stretches its tail to its full extent. Any creature that the missile hits it kills; the elephant alone it does not kill.

Claudius Aelianus, On the Characteristics of Animals, translated by Alwyn Faber Scholfield (1884-1969), from Aelian, Characteristics of Animals, published in three volumes by Harvard/Heinemann, Loeb Classical Library, 1958. Text copy-pasted from ToposText.org; full excerpt here.

The “Romanticize This Monster, if You Dare” Challenge.

I don't have the spoons to write out the whole story, but what about a suicidal person trying to get 'instant painless death' and the Manticore going "wait you're not attacking me I'm not going to sting you" and a montage of glimpses into their interactions, as the suicidal person gradually overcomes their depression and realises that they don't want to die they just want to run away from human civilisation; and the manticore going from "um you're weird but you're not attacking me so I'm not wasting my stingers on you" to "actually I like this human and I don't want to hurt them"

anyway shout out to transhet men and transhet people in general. you're amazing and you didn't "betray" anyone or "abandon" anyone or "become the enemy" - you deserve love, respect, and happiness

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georgeboleyn-againstovertime

Trans men have been demonized completely by the very community that’s sposed to protect an love them.

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sevenbillionlunatics-deactivate

It's unfortunate. I genuinely think they're joking and don't realise how much some people actually believe that shit and how it actually changes how trans folks view themselves.

I actually don't really think they're joking. I think that a lot of people in the queer community don't realize how much the political lesbian/radfem simplistic view of "men bad" has infected the community as a whole.

You see it in the "my sexuality is every girl and precisely one man" which is hugely widespread in the way m-spec women discuss their sexualities. (Which is not to say that a lot of women don't feel that way, just that when I've pointed this out to my friends, and how shitty it made me and other transmascs/men feel, a bunch of them went 'oh shit, you're right.') You see it in how m-spec women are made to feel like they should apologize for being attracted to or involved with men/mascs, and how lesbian/sapphic/queer spaces eject -- sometimes violently -- m-spec women in "straight-passing" relationships. (This also happens to m-spec mascs/men, but not so loudly, and in a different way.)

You see it in the long and storied way that transmascs and trans men have been treated in our community. This isn't the first time that trans men have been told they are 'giving up womanhood' and how dare they. There's a scene in The L Word, a show that ended 12 years ago, which has a character literally saying that to a trans man, that he's 'giving up the most beautiful thing' by transitioning, and that thing is 'being a woman.'

This isn't a new message, that men are the enemy, and that anyone who voluntarily chooses masculinity or manhood (whatever form of masculinity or manhood they choose) is a gender traitor, "joining the enemy," deluded, attempting to "opt out" of misogyny, or any number of other loathsome ideas. This spills over into the idea that transmascs/men have "aligned interests" with TERFs, that we don't actually face societal transphobia, that we aren't targeted by institutional transphobia in any way, that we're 'collateral damage' of the "real" transphobia that transfems face, that we magically just gain male privilege the moment we start transitioning, that we're never targeted by misogyny, that we don't face physical violence, that we've "joined the oppressors" and are somehow capable as a class of being the oppressors of transfems rather than simply another oppressed class (which is its own topic that deserves like, a whole-ass essay, but whatever) that transmisandry isn't a "real" thing and transmascs don't face any sort of specific-to-us discrimination or issues... and all of those ideas damage our ability as a community to discuss and ameliorate these sometimes-fatal and always-damaging ideas.

Hell, to listen to people within the community talk, you wouldn't think that JK Rowling's horrible essay didn't spend a huge chunk of time misgendering and gaslighting transmascs, or that one of the big "bibles" of TERFery (Ab*gail Shrier's 'Irreversible Damage') wasn't targeted very specifically, fucking laser-focused, on transmascs, including non-binary transmascs. And this all spills out from the idea that we don't face any 'real' oppression because we've 'joined the majority/oppressors,' and "men are bad," which is such base-level 1970s retro radfem nonsense.

And honestly, at the end of the day? It doesn't matter if it's a joke, and I'm pretty displeased with "oh they don't understand that it's serious and they think it's just a joke." These sorts of "jokes", levied at transmasc people, aren't okay. Maybe if it's just you and your buds who have given each other permission to shit-talk each other, and you know each other and have personal context with one another, sure. But in this sort of open, parasocial context where you have people who don't know these two transhets, it is always damaging, and saying "gosh I think they just think it's a joke" does the opposite of excusing it.

This lateral aggression shit is terrible and damaging to lots of people -- I honestly think there's no segment of the queer community that this doesn't directly damage, and we should challenge it whenever we see it, not make excuses or permission for it in the slightest way.

We are way, way past "I was being an ironic bigot." The idea that can be a thing needs to be permanently buried.

An electric toothbrush and an escalator are two things that can stop working and still accomplish their original goal.

Ah, wonderful! This post can help me illustrate something I’ve been trying to articulate for awhile: the concept of benign or unintentional abelism.

Escalators and electric toothbrushes are perfect examples of things that many able-bodied people assume exist for their own convenience, and this post is a perfect example of that unconscious assumption.

An escalator that has broken down is still perfectly functional, right? 

Well, sure–if you could have used the stairs to begin with

But for people like me, for whom the escalator was not a convenience but a mobility device, a broken down escalator is not functional. 

An electric toothbrush might seem like something that could be just as easily used turned off as turned on, but for someone with Parkinson’s, or any other number of nerve, coordination, or grip issues, the function of the electric toothbrush is a necessary feature, and without it, the task at hand becomes far more arduous (or even impossible). 

I’m not angry or trying to point out why this post is “bad” or “wrong”–I’m simply trying to point out that people who assume every time or energy-saving invention was created as a means to help able-bodied people be lazier should consider re-examining those assumptions. It might help you become more compassionate toward your disabled friends and family, or at least more aware of the struggles we face daily. 

I’ve had plenty of folks ask for examples of abelism and I am terrible at coming up with them on the spot, so here you go. This is a great one: assuming every modern convenience is only a convenience for everyone, when for some, it is, in fact, a necessity. 

^ When I heard that this is why all those infomercials show “impossibly clumsy able-bodied people” - that these random convenience devices are really made more for people with troubles like randomslasher describes, and it’s just able-bodied actors trying to act those mobility issues out - I kinda had to stop making fun of those clips.

And the reason they use able-bodied actors instead of showing real people with disabilities use the product is because if they did that, able-bodied people would see it and be like “oh what a neat product for people with x disability” and not buy it because they assume it’s not for them. And even though that’s true, the companies need able bodied people to buy it so they can make enough revenue to stay in business and continue to produce the product for people with disabilities.

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dnd-apothecary

^^ also the more able bodied people that buy or have a product intentionally designed for someone with disability is that it helps destigmatize it. Which is super important. 

Remember Snuggies? The blanket with sleeves? It was designed for wheelchair users/people with mobility issues so they could be warm and still use their arms without being trapped under a blanket. They were SO popular for a while, and everyone had one… which meant that if someone who was able bodied came over to your house and saw you had one too, it was less of a chance of being made fun of for it, and more like an opportunity for a conversation on about how they want one too. 

The slap chopper is also another great example. I know so many people who are able bodied that had/currently have one and sure it makes things quicker and easier for them, but someone with motor control issues or bad arthritis can use it. It won’t be an awkward “why do you have this thing” conversation. It is a “woah, I have one too!” or “I love mine, so glad you love yours too” sort of thing 

By selling/marketing them to able-bodied people, this makes it better for those of us who are disabled. It can destigmatize, which in turn normalizes it, which helps us become less Other and more Accepted. 

This is exactly why I was ecstatic that my mother got a weighted blanket at the same time as me. For her, it’s a comfortable thing that helps her fall asleep. For me, it’s a thing that keeps my ADHD from going into meltdown and keeps my anxiety in check.

Both the abled and the disabled having something that helps the disabled benefits everyone involved.

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littledeconstruction

this is such an excellent addition, because it illustrates something that’s often hard to show: many people who “aren’t disabled” still have bad enough issues that they would seriously benefit from assistive aides.

a huge amount of people have anxiety issues (for example), and most of them aren’t treated for it. they think it’s normal, or not bad enough, or they can’t afford treatment, or whatever.

whatever the reason, they don’t have a diagnosis, maybe they don’t even recognize their anxiety, but they still have anxiety, and they still could use a damn weighted blanket to help them calm down.

This is heart wrenching.

Nichelle Nichols (Lt. Uhura) has been suffering from Dementia for years. She’s lots most of her money, the home she loved and there is a fight for her conservatorship

Her sister has set up a GoFundMe site for her. The link is at the very bottom of this post. Please share this information.

Read the article below and please donate if you can. Even a couple dollars will help.

Y’all went hard for Free Brittany over conservatorship now do the same for Nichelle

So I read the entire thing, and this one is slightly more complex than “dad is abusive conservator.” So I’m going to lay out here what’s going on:

1) Nichelle has dementia.

2) In 2010, this guy approached her all “hey so I want to make this movie with you as a costar, very good contract, please accept.”

3) she did.

4) he was lying.

5) during the next several years he moved onto her property and became a squatter, billing all his utilities and expenses to Nichelle. In other words, she’s paying for the privilege of him using her property.

6) during this time he also managed to get her to give him power of attorney over both financial AND MEDICAL decisions. Much of her savings has just kind of vanished, and it seems likely he’s been leeching it away.

Okay. So, recap: this guy is NOT a conservator. He got power of attorney, which is actually a very good and useful thing when appropriately applied. (Basically, it means if you become incapacitated you’ve already selected a person to handle certain kinds of affairs for you.) In this case, however, it’s pretty clear POA is being abused and seriously misused.

7) Nichelle’s son managed to become her conservator, with the goal of kicking the deadbeat off the property and ensuring his mom has access to her hard-earned funds so she can be old with dignity. (In a perfect world, this is how conservatorship would always be used. His interest is in protecting the person, not making a profit.) He has become her primary caretaker.

I don’t know how advanced Nichelle’s dementia is, but I can tell you from experience that as the disease progresses, being a caretaker can become a full-time job, and that, yes—this is one of those extremely limited cases where conservatorship might actually be a good idea. My grandmother had Alzheimer’s (not all dementia is caused by Alzheimer’s, but all cases of Alzheimer’s are dementia), and nearly burned down the house once because she turned on the stove, forgot she’d turned it on, and went to take a nap. Having someone of sound mind who can make arrangements for things like appropriate in-home care so this doesn’t happen is deeply important.

8) deadbeat is fighting to get conservatorship removed—and possibly reassigned to himself. That part is a little less clear. What is clear is that he does not have Nichelle’s best interests at heart.

9) this fundraiser is to help with legal fees to get deadbeat off the property and help assist Nichelle and her son in securing what’s left of her assets.

So just so we’re clear: in this case we are actually fighting FOR a conservatorship. However, this conservatorship is to protect someone with an actual medical diagnosis that means she has diminished mental capacity to care for herself (literally, that’s what dementia is: loss of memory and cognition on a scale significant enough to interfere with daily life), and to ensure that what is hers, REMAINS hers.

Reblogging this version for the commentary, since people seem to be unclear about the situation.

✨ Blue Moon Tarot Reading ✨

I felt called to do a reading for our second full moon in Aquarius in a row, also known as a Blue Moon. Before I share my prompt I will also mention that during this particular reading two special things happened. The first was that during shuffling 3 extra cards fell out and I interpreted them not to match up with my prompt questions, but to complement them. The second was that normally my hands are cold or like room temperature but during this reading while I was pulling cards for the spread prompt, my hands ran so hot that the palms of them were red and felt as if they were glowing -- that has never happened before during a reading 🔥 . My prompt for this Blue Moon was split into three separate questions : how can we hold space for one another, what is one way we can practice acts of love collectively, and what is one way we can let down our guard to practice holding space specifically for vulnerability?

1) Mother of Cups : nurturing, compassionate, comforting, kind

2) The Hanged Man : willing sacrifice, release control

3) Three of Pentacles : teamwork, collaborative building, swift progress

________________________

Complementary Cards :

1) Three of Wands : rapid growth, expansion, establishing strength

2) The Sun : success, clarity, positivity, conscious

3) Daughter of Pentacles : new opportunity, desire, material venture, enthusiasm

______________________

Themes in the complementary set of cards can be achieved by practicing collaborative efforts and acts of love with the themes in the prompt's spread.

Does anybody even still follow me?

Hi all, it's Socks, and the past two years have been... Fucking wow.

You may have seen my announcement that I'm getting married, yeah that didn't happen. In the end, the police had to drag her out of my home on four separate occasions, including the time she kicked in my door.

It's okay, I'm safe now, it's over.

I repeat, I am safe, locks have been changed, legal measures have been pursued, I am safe.

But yikes what a ride it's been.

@queerdo-mcjewface I would love to see your dog. I have pets as well now!

@jurinjo hmm it won't let me tag you, but yes, this is Deto, and his brother is named Sushi.

Nobody worry, I would never keep rats alone, I just like this picture. It's hard to get a nice one with both of them at once.

Does anybody even still follow me?

Hi all, it's Socks, and the past two years have been... Fucking wow.

You may have seen my announcement that I'm getting married, yeah that didn't happen. In the end, the police had to drag her out of my home on four separate occasions, including the time she kicked in my door.

It's okay, I'm safe now, it's over.

I repeat, I am safe, locks have been changed, legal measures have been pursued, I am safe.

But yikes what a ride it's been.

@queerdo-mcjewface I would love to see your dog. I have pets as well now!

Does anybody even still follow me?

Hi all, it's Socks, and the past two years have been... Fucking wow.

You may have seen my announcement that I'm getting married, yeah that didn't happen. In the end, the police had to drag her out of my home on four separate occasions, including the time she kicked in my door.

It's okay, I'm safe now, it's over.

I repeat, I am safe, locks have been changed, legal measures have been pursued, I am safe.

But yikes what a ride it's been.

Currently thinking about opening readings this summer (June throughout August). Let me know if you would be interested 🕊️💕

Pricing*

1 card -> $5
3 card bundle -> $15
5 card bundle -> $30
8 card bundle -> $60
Custom Spreads -> $20 and up
Spiritual Profile -> $15 and up
  • birth chart
  • crystals / herbs
  • elemental correspondences
  • music + other self care associations
Dream Divining -> $8 and up
Candle Lighting -> $3
  • tea light candle
  • incense
  • focused thoughts / prayers / blessings as requested

*all prices are based on energy, supplies, and experience used by the person providing the requested reading

Booking My Services

DM me : "hey I think I need a reading / I'd like to book a reading what does your schedule look like?" As more people book me I'll start posting weekly or biweekly updates . I have 2 readings at the end of this week to do but after June 11th my book is open for new clients 💕

✨ Current Schedule : I see clients June 1st through August 31st ✨

Inertia?

I have a hard time switching activities. Even if I want to switch to something I want to do, it feels like the previous activity has built up a bunch of inertia and now can't be stopped. Does anyone else get this feeling? How do you fight it?

Hi, I'm Lighty!

Hi everybody, I'm Lighty! I'm a girl (she/her) and I'm in my 30s. I'm marrying the amazing @sockknitterporg in just a couple more years. We're waiting a bit because Socks is making our wedding dresses by hand, isn't that amazing?

Anyway, they twisted my arm to get a tumblr because, according to them, there's an amazing autism community here and I'd really like to get to know like-minded people and make some autistic friends.

I've struggled with my autism for a while, and it's taken me even longer to see it as something that makes me who I am and makes me proud to be me. My parents were horrible about it, and didn't really teach me anything about how to function as an adult human being in a (neurotypical-based) society.

I'm hoping that the #actuallyautistic community here can help me learn some coping strategies that will allow me to interact with the neurotypicals a bit better, and take better care of myself instead of just muddling through. (Socks actually had to help me write this because I really struggle with knowing what to say in these kinds of situations.)

I like anime, especially Yugioh and Pokemon. I like video games, like Monster Hunter and Animal Crossing. I like to listen to K-Pop but I wouldn't describe myself as "a K-Pop fan", but I'd like to get to know some people in that community, too. I'm hoping to learn calligraphy and pixel art, though I'm definitely a total beginner at both of those things.

We live in England, but I'm totally open to making friends around the world. I'm from a city called Hull (but we don't live there any more). I'd like to make friends, and I'd like to get to know all of you! Feel free to follow me or drop by my ask box to introduce yourself!

Hi, I'm Lighty!

Hi everybody, I'm Lighty! I'm a girl (she/her) and I'm in my 30s. I'm marrying the amazing @sockknitterporg in just a couple more years. We're waiting a bit because Socks is making our wedding dresses by hand, isn't that amazing?

Anyway, they twisted my arm to get a tumblr because, according to them, there's an amazing autism community here and I'd really like to get to know like-minded people and make some autistic friends.

I've struggled with my autism for a while, and it's taken me even longer to see it as something that makes me who I am and makes me proud to be me. My parents were horrible about it, and didn't really teach me anything about how to function as an adult human being in a (neurotypical-based) society.

I'm hoping that the #actuallyautistic community here can help me learn some coping strategies that will allow me to interact with the neurotypicals a bit better, and take better care of myself instead of just muddling through. (Socks actually had to help me write this because I really struggle with knowing what to say in these kinds of situations.)

I like anime, especially Yugioh and Pokemon. I like video games, like Monster Hunter and Animal Crossing. I like to listen to K-Pop but I wouldn't describe myself as "a K-Pop fan", but I'd like to get to know some people in that community, too. I'm hoping to learn calligraphy and pixel art, though I'm definitely a total beginner at both of those things.

We live in England, but I'm totally open to making friends around the world. I'm from a city called Hull (but we don't live there any more). I'd like to make friends, and I'd like to get to know all of you! Feel free to follow me or drop by my ask box to introduce yourself!

Hi, I'm Lighty!

Hi everybody, I'm Lighty! I'm a girl (she/her) and I'm in my 30s. I'm marrying the amazing @sockknitterporg in just a couple more years. We're waiting a bit because Socks is making our wedding dresses by hand, isn't that amazing?

Anyway, they twisted my arm to get a tumblr because, according to them, there's an amazing autism community here and I'd really like to get to know like-minded people and make some autistic friends.

I've struggled with my autism for a while, and it's taken me even longer to see it as something that makes me who I am and makes me proud to be me. My parents were horrible about it, and didn't really teach me anything about how to function as an adult human being in a (neurotypical-based) society.

I'm hoping that the #actuallyautistic community here can help me learn some coping strategies that will allow me to interact with the neurotypicals a bit better, and take better care of myself instead of just muddling through. (Socks actually had to help me write this because I really struggle with knowing what to say in these kinds of situations.)

I like anime, especially Yugioh and Pokemon. I like video games, like Monster Hunter and Animal Crossing. I like to listen to K-Pop but I wouldn't describe myself as "a K-Pop fan", but I'd like to get to know some people in that community, too. I'm hoping to learn calligraphy and pixel art, though I'm definitely a total beginner at both of those things.

We live in England, but I'm totally open to making friends around the world. I'm from a city called Hull (but we don't live there any more). I'd like to make friends, and I'd like to get to know all of you! Feel free to follow me or drop by my ask box to introduce yourself!

The main bulk of my suffering is directly related to the manufactured "opiate crisis" that has caused untold pain and suffering for so many millions of people for so many, many years. In this essay, I intend to place my experiences in their proper context, as one of a sharply growing series of victims of medical malpractice stemming from the fundamental shift in our society from seeing pain patients as people to be treated, to deriding them as addicts to be suspicious of.

Though it says volumes about our society that we see addicts as fundamentally 'bad' people who deserve homelessness and death instead of as human beings, often times human beings who are suffering greatly and turn to the only thing that makes life even mildly bearable. But that's neither here nor there. (For more information about addiction, see https://tinyurl.com/rat-park )

Our story begins in 1996, when Purdue Pharma (Stamford, CT, USA) released OxyContin, a sustained release oxycodone preparation that is also sold here in the UK. In the US, where such things are legal, it was aggressively marketed and promoted as less dangerous and less addictive than other opiate preparations. (Source & more information about OxyContin's marketing: https://tinyurl.com/oxymarket )

Anyone who thinks a $200 million a year marketing campaign would not spill over to the UK is more than merely obtuse, but likely willfully ignorant. The entire 'opiate epidemic' is an American import, and it started there: with an unscrupulous American company that would stop at nothing to make money.

Lulled into a false sense of security by Purdue's claims of minimal risk of addiction, doctors began prescribing OxyContin much more liberally and for much more than they originally would have. This increased availability set many people up for addiction and overdose deaths.

To most people, that is the bulk of what the 'opiate crisis' is. But there is a secondary crisis unfolding quietly behind closed doors. In the USA, there are "Don't Punish Pain" rallies that at least try to draw attention to the situation ( https://dontpunishpainrally.com ), but here in the UK we are entirely forgotten and buried under the British 'stiff upper lip' mentality. It is completely hushed up, no one talks about the fact that the pendulum has swung too far in the opposite direction. (For example: https://tinyurl.com/opiate-pendulum )

The government and/or the NHS have enforced involuntarily tapering of chronic pain patients' medication. Medication we need in order to not spend our lives screaming in agony. The pain management clinic has already warned me that it is, direct quote, "when, not if" I will find my own medication terminated, ready or not.

But there will be no 'ready'. Chronic pain does not get better with time. Chronic pain does not go into remission. If you know someone with chronic pain who appears to be 'getting better', I can promise you it is merely that the sufferer has learned to better conceal it. It's a saying in the chronic pain community, "We don't fake being ill. We fake being well."

We have learned that the average person only has about two weeks of compassion in them, after that you're treated as a freak for not getting better already, or outright accused of malingering. After all, with all of modern science, can't you just go to the doctor and get a pill and be done with it? Our concept of illness is either 'you go to the hospital, get treated, and come out okay' or 'you go to the hospital, waste away, and die'. Chronic pain patients, who never get better, but aren't actively dying, don't fit in to our society's 'concept' of illness.

People who offer to help us out for the social brownie points of helping the poor cripple soon discover that we're not going to die, we're going to continue to need help for the forseeable future. Rather than gracefully admitting that they don't have the ability to help us in perpetuity (which would be perfectly understandable!), most people choose to lash out at us, we must be abusing their kindness, they helped so we must surely be better by now. Compassion fatigue seems to hit every single human being that interacts with us, as if merely existing while disabled is wearing on their ability to remain civil. (Compassion fatigue: https://tinyurl.com/2-week-fatigue )

Doctors have even less compassion than that. In the backlash of the 'crisis', they have begun to treat anyone who complains of pain, unilaterally, as a drug seeker. And those of us already in treatment? Are addicts in need of rehab. (More examples: https://tinyurl.com/drs-no-compassion )

Despite study after study (Studies: https://tinyurl.com/no-taper ) showing that tapering chronic pain patients unequivocally causes severe harm, up to and including death, the pain management team said to my face that I am, direct quote, "addicted to heroin" and "no different from my four year old grandson, demanding a choccy biscuit because he doesn't know they'll rot his teeth. And I have to smack him and tell him NO! And I'll smack you, too, if it'll get you off those drugs!" (Somehow my complaint that a doctor had literally smacked his hands in front of my face to demonstrate that he was sincere in his threat to physically assault me.... mysteriously got lost.)

I have been denied treatment for other (non-opiate) methods of reducing my pain because, direct quote, "it doesn't matter as long as you're on those drugs, opiates actually make you more sensitive to pain in the long run, so there's no sense trying anything else if you won't get clean." They talk to me like taking my medication responsibly, as prescribed, is the same as shooting up black tar. All in the hopes of bullying or shaming me into "voluntarily" tapering.

Honestly just living under these conditions alone would be enough to snap my mental health in half, but you have to remember that I'm not only facing all of this systemic bullying and professional misconduct while also living with pain that has often been compared to late stage cancer and chemotherapy ( https://tinyurl.com/fibro-chemo ), as well as debilitating fatigue, and a shroud of fog hanging around my brain and clouding my memories and judgments (and at times, my ability to speak English). Everyone's first reaction is "did you report them? you should report them. why didn't you report them!" as if I'm too stupid to have thought of that myself. But I don't have the energy for the lengthy bureaucratic nightmare that is dealing with the NHS's administration, especially not when I could have my entire life destroyed by a doctor's bruised ego penning into my file "patient was uncooperative and combative, suspect drug abuse".

It's only a matter of time before I choose suicide over another sleepless night of laying in bed and praying for death. And when that time comes, I hope that my name is added to the long, bloodstained list of people who have killed themselves not out of any sort of depression, but because their entire existence is built on pain and suffering and enough becomes enough for the last time. Drop my body on the steps of the CDC, which is the main driving force behind the opiate witch hunt. Maybe death will at least bring me some measure of peace.

Hi, I'm Lighty!

Hi everybody, I'm Lighty! I'm a girl (she/her) and I'm in my 30s. I'm marrying the amazing @sockknitterporg in just a couple more years. We're waiting a bit because Socks is making our wedding dresses by hand, isn't that amazing?

Anyway, they twisted my arm to get a tumblr because, according to them, there's an amazing autism community here and I'd really like to get to know like-minded people and make some autistic friends.

I've struggled with my autism for a while, and it's taken me even longer to see it as something that makes me who I am and makes me proud to be me. My parents were horrible about it, and didn't really teach me anything about how to function as an adult human being in a (neurotypical-based) society.

I'm hoping that the #actuallyautistic community here can help me learn some coping strategies that will allow me to interact with the neurotypicals a bit better, and take better care of myself instead of just muddling through. (Socks actually had to help me write this because I really struggle with knowing what to say in these kinds of situations.)

I like anime, especially Yugioh and Pokemon. I like video games, like Monster Hunter and Animal Crossing. I like to listen to K-Pop but I wouldn't describe myself as "a K-Pop fan", but I'd like to get to know some people in that community, too. I'm hoping to learn calligraphy and pixel art, though I'm definitely a total beginner at both of those things.

We live in England, but I'm totally open to making friends around the world. I'm from a city called Hull (but we don't live there any more). I'd like to make friends, and I'd like to get to know all of you! Feel free to follow me or drop by my ask box to introduce yourself!

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