Saturday, August 20, 2022
Friday, December 31, 2021
I've gotten covid
Saturday, November 27, 2021
journey of healing
Saturday, November 20, 2021
Lol I already fucked up
Tuesday, November 16, 2021
wow
Sunday, May 17, 2020
progress
Friday, October 18, 2019
updates
Monday, September 23, 2019
Bleh
If anyone can donate to my PayPal, that would help me be able to see my therapist on Friday. I have had an abusive experience recently and my medical credit card is in the negative, so I don't have any way to pay for my session.
We haven't found a house yet, but we have semi stable housing for now. I'm probably going no contact with a family member that was shitty to me cuz I don't want to tolerate abusive behavior. I am safe, and husband has been very supportive of my decision. I am exhausted because the situation put me into a flare later that day.
I hate to beg right now. Unfortunately I don't have a lot of family financial support and I'm chronically sick, so doctors appointments add up, and so does medication. I haven't been able to go to therapy for about a month, when I should be there once a week per my doctors orders. Hubs works two jobs and we still can't afford meds and copays. I cannot work because of my health. So I need community support to help us get through this period of time.
My links are in the sidebar, or go to girlysatan.com and try the links there. I appreciate any help at all and there's a variety of places you can donate.
Tuesday, August 6, 2019
Oh jeeze
I am freaking out about my situation. TL;DR too many bills, not enough income since I'm unable to work. If you can donate, please help.
I am in a bad place still with finding housing. We can't find a place to live because it's impossible to find something in our range. I also have $130 electric bill from the air conditioning because I can't maintain my body temp correctly (thanks dysautomia, and my hEDS). I also have gotten a carecredit bill for when my dog died that's about $600. The lowest cost pain meds I can get are $30 which lasts me about a week. I can't work. My body is a piece of shit that doesn't work but I'm still not on disability yet because it's a long process.
I also can't fucking stand that every time I get up or move around I injure myself. My legs and ankles are covered in bruises and my hands are covered in cuts because I keep accidentally hurting myself. I can't do dishes anymore because I keep accidentally cutting my hand on everything. It's almost like my collagen sucks so I'm fragile and take a long time to heal or something.
I redid my tumbler and I think I'm gonna put most of this emotional stuff on there. I need something to talk about how the world is ending and everything is terrible.
But at least I'm drawing again. I been working on making some fan art because I need to focus on something I can control. Hopefully I'll be posting something soon.
Still working on AlbiaSquared, don't worry! Been messing around with insects a bit to add some life into the game. Also my big project is the different birds I made.
Monday, June 24, 2019
If you're suffering, keep going
I'm sorry, I know I have been screaming about how difficult shit is here. It's been a ridiculous struggle.
I might have secure housing soon. I'll have a basement but everything is on one floor. This is going to improve my energy a lot and I'll be able to work on things I want to work on again.
I have my diagnosis and I'm working on disability paperwork.
My psych meds are at a great spot. They aren't too high so I'm not experiencing increased body heat, which was why the last few summers I've been having a really hard time with the heat. This year I don't feel like I'm constantly sweating, thank the gods.
Therapy is at the point that I don't need to go every week anymore.
I am working on things I like even though it hurts to do it.
Pain meds are still out of my grasp but kratom and medical marijuana seems to be helping some of the pain. I am at least able to get my hygiene taken care of.
Did you know that most of those tv infomercial things are for people with disabilities? Lots of stuff like slapchop and the vegetable salad bowl cutter help people like me who don't have much strength be able to prepare food. Even the snuggy was made for limited mobility people. I'm still finding more stuff that can be useful and I'll put it in a wishlist. I used my grabber the other day to clean up stuff off the floor and my apartment isn't a hot mess anymore. These mobility supportive stuff really helps.
I have opened up AlbiaSquared again and started working on animals again. Some of these guys came out beautiful and I can't wait to release what I'm working on.
I have added more stuff to my Etsy store so please look! I really love the pieces I have made and I hope you'll consider picking something up or commissioning me with an idea for a nerdy piece. I've started making two more coasters yesterday. I'll also be streaming some of the code work this week for AlbiaSquared. Please consider donating! I also opened up a channel in discord so you can talk to me about any bugs you found.
Things are improving but it's still rough every day. I'm happy to be doing things I enjoy again.
Wednesday, June 12, 2019
yikes
We have a month left to try to find a home and put an offer in. Most of the houses I have been having problems with is because they are not accessible enough or they have something that violates FHA. Hooray for discrimination!
Capitalism doesn't care about us, because I have genetic health problems that cant be controlled.
The planet is on fucking fire though, and I'm watching society collapse in real time.
I have lost all my fucks. I have no more fucks to give.
Maybe someone will magically buy me an accessible home, and I wont have to panic about having a stable living situation. The most accessible houses are in the 80k range and we are only able to look at 75k or less because I cant work anymore. We cant rent anywhere on Jeff's income alone. I dont know what to do anymore. I just want to live in west Cleveland. I just want to live my last miserable years in one fucking place while my body falls apart, and be able to use a wheelchair to get around in my house.
People with EDS age faster in some ways. I lose my mobility as joints become less stable and more prone to dislocating or shifting. I dislocate or partially dislocate large joints at least once a month. My ribs slipped a couple times this past month just from how I was sitting; I will be just chilling working on art, or just watching fucking Netflix, and I suddenly can't breathe. I hate it.
When is society going to pick up disabled people and support them? Probably never.
I'll probably be homeless eventually, as happens to most people with health problems.
my life is fucked lmaaoooo
Tuesday, May 28, 2019
Frustration
If I wasn't disabled I would have enough money to take my dog to the vet and we wouldn't be struggling to find a home. If anyone can spare please donate. https://www.paypal.me/ChristineShara
Thursday, April 11, 2019
Some days are easier than others
Some days my body is in so much pain I can't really sleep. Other days I'm too exhausted to stay awake even with an 7 or higher pain, and I just struggle to stay asleep.
Today my body is on fire. I irritated my ulnar nerve so one and a half of my fingers got electricity shooting through it this second. I'm actually using Swype keyboard because then I can use a pen or just my finger to write, instead of typing everything. I could even use voice if I wanted and I probably should. Anyway, this nerve pain blows and I'm fucking over it.
I'm going to need to try another pain management place because with the EDS diagnosis it should help them take me seriously. But I was also basically semi conscious during those last couple months at work and no one helped me then so I have a lot of doubts. I just fucking can't anymore with this nerve pain. It's so bad I want to cut my arm off.
I think the worst thing about this is I painted for a couple hours and my reward is this bullshit pins and needle garbage all the way down my arm. I wanted to fucking paint so my body says "fuck you for making me do things".
My mental health is okay ish but lately I have been feeling very little hope because my body sucks so much. I had to give up on my dreams of being in the medical field at all. But after my burnout it's impossible to go back. Maybe I'll be able to get the correct meds so I can work in the lab again part time but I really doubt any one is going to help. Maybe I could work in a wheelchair, but I really doubt I'll get hired. Regardless of the law, people would not hire me knowing I'm disabled. I had enough discrimination at the Cleveland clinic for my partial disability, and every lab was real excited about me until they learned I had limitations. That's just how the fucking US is.
Someone just buy me some art supplies for my store so I can stop thinking about how much everything is stacked against me. I am afraid to hope for anything anymore.
Wednesday, March 20, 2019
If I die, it was because I couldn't take the pain anymore
I am no longer on muscle relaxers which means my muscles are gonna start twitching again. My fatigue is going to triple and I already feel like I'm carrying a hundred extra pounds. Most of my days are going to be spent in bed because I'm either too dizzy to stand or the fatigue is so bad I sleep for most of the day. This is what I get for asking for help, getting my meds taken away again. I'm never going to have a normal life if doctors keep ignoring what I'm going through. Is the pain not enough? Is me not working enough? Is me spending the rest of my life in bed enough to get them to fucking do something? Probably not. The only medical relief I can get for the pain is medical marijuana, and even if it magically made it so I could function again, ill never be able to work because people can still get fired for using medical. So either way I'm fucked. What's the fucking point in being alive if doctors won't listen to me. I have genuine pain and fatigue that interferes with my daily life and I'm ready to pack it in and just die cuz I can't deal with it anymore. I have no quality of life anymore because I can't even enjoy simple things like doing art or writing. Instead I have to think about my pain constantly or drug myself to sleep so I don't have to deal with it. But even then, the pain still wakes me up every couple of hours no matter how much otc sleep meds I take.
If I end up dying, I love you all but I couldn't take the pain anymore. I just want to be able to enjoy some games and make some art and grow a beautiful garden. I just want to be able to write again, even if I could never work again. It's not your fault, it's on the health system. I've been struggling for over a decade to get treated and I'm back to no meds again, so clearly they won't help me. What do you do? I just want my suffering to be reduced enough so I could do things that make me happy, but I can't even have that. The world still has beauty, but my suffering keeps me from enjoying it. It's a sad day when an artist can't create anymore.
Friday, February 22, 2019
Shameless Store Promo
I would like to use some of the bigger pendents that people can put their initials in. Ill have to see how much space they take up in the different pendents, but there are some large ones so I'm pretty sure that two names could be in there or a couple short words. This circle piece could definitely fit some initials in it with the blood type.
If you want to donate to my store you can go to this wishlist. I wouldn't have been able to do it without your donations, so please consider sending me more stuff to work with. I am slowly getting through all my shop ideas, more or less. Unfortunately I don't have a lot of energy because of my health to work every day, but I'm slowly getting there. Art brings me joy, which helps a lot.
Be kind to each other, everyone is in pain.
Tuesday, February 5, 2019
Therapy did some good
I have suffered so much abuse from every aspect of my life. I honestly am not sure why I am still alive. I live in pain every day which is incredibly traumatic. The physical pain is enough to make me want to end everything, but the toll on my soul is devastating. I have suffered sexual assault, domestic abuse, neglect, even some physical assault. These are all incredibly terrible just on their own and it kills people daily. And I have met some incredibly strong people who have suffered much worse than I have and I marvel at their strength. Its not a competition, terrible things happen to people all the time because life is fucking terrible. Suffering is not just the human condition, but every living things condition.
We are hardwired to default with happiness because life is so fucking bad. People who are not depressed actually see positive things more frequently than the negative things. Life is so cruel and existence is so awful, we literally had to evolve to look for the good things in life so we wouldn't kill ourselves. Innocent creatures suffer and die every second of every day and that is terrible.
I have nightmares sometimes, where I am supposed to clean up these aquariums and cages full of pets that have starved to death in their cages. When I'm particularly emotional, they are half evaporated tanks that have dead fish floating in the little water that is left. When I really want to torture myself, I see mummified remains of lizards or mice or whatever else can live in a terrarium. The worst though is when I dream about dozens of bird cages that are just filled with dying birds or dead birds and a few that are somehow alive among the corpses and I try to save them every time. Why do I try to save them every time even when I know I'm in a nightmare? I can't let suffering happen in front of me and I want to unleash torment on those that inflict suffering for fun. So I always try to save those poor dying animals that didn't deserve what happened to them. Just like I never deserved the abuse I suffered.
There is one thing that pain has shown me. The most divine thing you can do is have empathy and care for others. Someone can be experiencing something I could never understand, but I understand pain. I can recognize pain even if I cant understand the details, and everything knows what suffering is, so I can connect that empathy there. Everyone deserves kindness because life is fucking cruel.
Someone is hurting you because they are hurting. Also, you hurt people because you are hurting too. Its good to recognize where you have hurt someone else and if you can apologize for it, you should.
Thanks for coming to my therapy writings.
Friday, January 4, 2019
Please Ignore this Desperate Plea for Help
My insurance told me that they didn't approve covering one of my doctors visits because the office put the wrong code for the visit. I tried to explain that my insurance would cover the visit if they resubmit it with the correct code for the visit and everything from that would be covered. But instead I was stonewalled, treated like garbage, and also interrupted every time I tried to explain what I needed them to do. Dude, I am so fucking tired of insurance companies and doctors offices pushing me around because one or the other person just doesn't care that I cant pay the bill anyway. My insurance will cover it, but because I am easily confused due to my illness it makes it impossible for me to manage the health system. I am ridiculed and pushed around instead of helped. What the fuck happened to this place that I cant get some simple help with fixing a mistake that other people made? Why do we treat people this way?
Part of being easily confused is frustrating because I know when someone is being shitty with me, but I cant process anything in response. Treat me like a human being. Give me some time to understand what you're saying. I'm not an idiot, but I cant process information very well. I am tired of people being shitty and condescending to me because I have problems communicating.
I am too sick to work. I can't work in what I used to love because my inability to remember can kill someone. Being confused easily is not a good thing when you are trying to test biological samples. At this point it's so bad that I can hardly remember what task I was going to do five seconds before. Its not a problem with me when I'm working on coding, but that can be real bad for someone who tests blood for a living.
Also because I have problems trying to remember, I actually forgot to pay my utilities last month because I literally thought I paid it. Now they want the money for two months worth of utilities in my gas and electric and we cant afford it because we were already living paycheck to paycheck. I have like $300 due in utilities and I have to hold that off because I needed to take my sick cat to the vet.
I am powerless. I feel so fucking powerless because my disease makes it impossible for me to manage my life that most people would never have problems trying to resolve. I have two degrees and an associates and I cant work even though I have so many qualifications. I feel like I was put in someone else and any accomplishments I made don't matter at all. I would like to get help so I can be put on disability but I'm too confused to manage the system on my own. I need help but I don't know what to do or who to talk to. I have considered divorcing my husband so I can get on SSI because we make too much. I cant even get food stamps because we make too much. I have lost 20 pounds because I have to stretch my food budget for myself so I can take care of my animals. I used to be able to take care of them. I am afraid that I can't be the fur mom they deserve anymore because I am in a broken body. My bird is bonded to me which means a lot of distress for her if I give her to someone else that can take better care of her. I shouldn't have to throw everything in my life away because I am too sick. Besides, my animals have been one of the only things that kept me alive. Do I need to sacrifice everything that comforts me when I have so little to hang on to in the first place? I don't have enough money to pay my bills so apparently that's what I need to do.
I don't know how to get help. I'm afraid that this disease is going to kill me. The pain I feel constantly drives me to consider ending everything. My powerless life makes me want to just cease to exist. Somehow I am still around regardless of all that, but my disease is going to kill me one way or the other.
This reality sucks.
Tuesday, January 1, 2019
Everything hurts and I'm dying
The last two weeks have been really rough on me. I been around a 9 most days, and barely have been able to get out of bed. Been averaging 500 steps for the whole day. I am so miserable. I tried a percocet to see if it would help my pain. It did nothing at all. So really this tells me I should be on stronger pain meds, because whatever I'm doing isn't doing shit to help with the pain. I'm at a complete loss. I also managed to be late on some bills because I thought I paid them, but my fibro fog brain was just tricking me. I need to come up with money out of nothing because my disease screwed me over again. I have no idea what to do. Being disabled is so hard and if I want to get SSI I discovered today that I likely need to get a divorce. This country punishes people who get sick. I didn't ask to be this way.
I'm so so so tired. I'm tired of being in pain and having no life. What can I do? I am trapped in poverty because of illness. I'm stuck in my bed because of illness. I plan to stream the next few days because I have to beg for money again. I don't see the point in trying to live in a society that punishes me for existing. I'm trapped.
I think it's time to write articles about how screwed so many of us are. It's not just me, it's so many people.
Tuesday, December 11, 2018
Broke and chronically ill
Well I couldn't pay my copay today for therapy. Luckily they let me pay next time.
I desperately need support so if anyone could donate so I could pay my medical bills I'd gratefully appreciate it.
Hopefully I'll stream today and maybe earn your pity for being so sick.
https://www.paypal.me/ChristineShara
Thursday, December 6, 2018
I Am Alive Somehow
I need to have a serious conversation with you.
Earlier this year I almost killed myself.
Being chronically ill and trying to work full time made me sick and made me so sick I almost died.
What choice did I have? We can barely afford food right now on one income, so I have been begging friends and family for money to keep us afloat. I was fired in January and have been struggling to find work, not because I'm ready to go back but because I have to. I shouldn't be working, I can tell you that much. My body is in so much pain and in January I probably would have killed myself because my psych meds were not being well monitored at the Cleveland Clinic, even though I was doing everything they told me to do. I struggled to get them to listen to me about the meds not working, or how I needed a better time for group just to get access to my medications, but since I worked nights it was impossible to go to group. They wanted me to be there at three or four in the afternoon and they didnt have times earlier or later, which was like asking a regular day worker to show up for group at 1AM. I just wanted to have psych meds so I wouldn't kill myself. As much as group therapy helps in some situations, it wasn't enough for me and when I asked to have more one on one therapy I was refused. Instead of using all the tools I wanted to use for my own mental health I was being told no? Why?
This is not an unusual story. Chronically ill people have to deal with the struggle between being too healthy to get disability and too sick to work. Most people need to divorce their spouses otherwise they wont get their SSI, which is a bunch of shit. Our society is built around making profits, and if you cant make profits, you cant survive.
Only here in the US do people go into debt because they are sick and cant help it. Capitalism makes you pay for everything. Eyes not good at reading? You have to pay for glasses. Hard time getting around? Pay money for a medical grade cane. Want a tiny robot to vacuum your house for you? its only like a couple hundred dollars, we don't care if your legs don't work, only lazy people don't clean their own house. Have to work in bed? This table only costs 120 dollars because its got wheels to push it out of the way when you need to sleep. Not everywhere is wheelchair accessible, which limits access to houses, restaurants, things we need. Things human beings need. Vets missing limbs aren't getting their fucking check for defending this country. If you can afford insurance, you still pay a deductible to get access to your meds at a discounted price, which you still have to pay for, and if you cant afford it, NO ONE CARES.
I paid off my credit card in April. I have almost hit the limit at the end of this year. This card I only use for necessities like, taxes, medication, medical appointments, and food. I literally cant afford things I need to survive because I cant work, but I cant work because I have the bad luck of shitty health. I literally worked myself to near suicide, got fired, lost all my meds, lost my health insurance, lost every fucking thing in my life that gave me hope.
I have good insurance now, thanks to my spouse, and I still racked up all this medical debt just trying not to kill myself. I don't know how I survived not having psych meds for so long. I was sure I would die at any point because I thought I would finally snap from the excruciating pain and end everything. Once I got on insurance, I was able to see a doctor, get my psych meds, get my meds to help me walk through the pain I experience every day, and get to appointments to try and figure out what is causing my chronic pain. I have fibromyalgia diagnosed already, but I suspect something else may be related to the extreme bone and joint pain I feel all the time. So far I just have a diagnosis as chronic pain and we're struggling to find ways to deal with it.
I dont want to die anymore. I still feel pain all the time and little helps it. I'm trying to find things to do but chronic illness means I can only do a little each day. I have little hope for my situation improving and I don't think I'll be able to get disability on the fibromyalgia and chronic pain diagnoses alone. I'm trying to find answers but there's little I can do. This is a sad story but not that unusual.
I have a friend who worked herself to exhaustion. She lives in chronic pain. She also uses up all her sick days and takes time off without getting any money so she can keep her job and have enough hope to survive. I have other chronically ill friends who work themselves to the point of passing out before they will stop because they cant. We cant stop working because we wouldn't be able to get treatment just to survive. My mom should probably be retired by now and has a ton of chronic illnesses, but she still works because she cant afford to just stop. I've talked to people online who have chronic illness and are struggling to get SSI, but because they worked in the past several years they aren't eligible. No one that is chronically ill can just stop working and still get support for their health. We are completely and utterly fucked in the land of opportunity that is the United States of America.
I have student debt to pay off still, a car, rent, my one credit card, and utilities. I dont think I can go back to work because I'm not functional enough most days that I could put people in danger. I miss my job and my friends I had. I almost died but before I broke from the pressure and exhaustion and pain, I was hopeful.
Now I just hope I can get out of bed the next day, to do one thing I like; play a game, read a book, make some art, even just play with my bird.
I want to share with you my logs from the past year. I even recorded how many steps I take now, and bad days I take maybe 300 steps in the entire day. But there are many days that you can see where I take more than that, even at a a level 8 pain. It's not that the pain isn't that bad, its that I have to do things that day, regardless of the pain.
I just wanted to tell you all why I have been missing for a while. Why I haven't been active in Creatures lately. I think if you see what I have been struggling with, maybe you can soften any attitudes you have towards your own friends and family with chronic illness.
https://www.dropbox.com/s/thmq9v7800qffg2/1544063237981_Christine_Sharas_PainScale_Report.pdf?dl=0
Edit: I have my medical marijuana card btw, don't hate on that.