My Shop l Ko-Fi l Prints l AO3 | Wishlist Renee, she/her, 40s, married, pagan, Disabled, queer, quilter, gamer, writer, watercolor painter, science junky, Dragon Age lover, progressive socialist Democrat. If you are a Trump-Humper, nazi/neo-nazi, racist, antisemitic, radfem, ableist, (LGBTQ+)-phobic, you have no place being here! Reproductive rights are human rights! Trans rights are human rights! Black rights are human rights! Before sending me an ask begging for money or that I share your GFM, read this. Failing to do so will result in me reporting the ask and blocking you immediately. If enough people report your asks as spam, your account will be closed, so think carefully before spamming my inbox with begging. I have reported and blocked more than 100 accounts for sending me these asks. Quilt Commissions: OPEN, April 1st to May 1st Background is a closeup of a painting I made. Avatar is my OC Ghanima Lavellan created by Lagunanegra.
It has been suggested I make a post to pin at the top, with some info for anyone who decides to stop by.
First, I have my most important links at the top, but if you don't feel like scrolling up, here you go.
My Kofi Page - here you will find my gallery, shop, and the options for supporting me. This includes a monthly option, called a membership. My Kofi page is like Etsy and Patreon rolled into one, with some extras, and much more user-friendly. Selling my work also reduces the mentality of my being a burden, and thank you for making that load much lighter for me. Pssst...my members get automatic discounts on shop listings and commissions, and some things are available only to my members.
My Throne List - this is a list where you can purchase items for me, and do so anonymously. I have quilt-related things, stuff for hEDS, egift cards, and other randoms. My being Disabled and my husband being the only source of income aside from my fixed income, I don't have much opportunity to shop for anything that isn't 100% necessary.
My AO3 - I write Dragon Age fanfiction, namely the smutty stuff. Because I can. Fair warning: I like it explicit and mixed with humor because life is weird and funny. You will need to be logged in to read anything I post. My account is locked in order to prevent AI from scraping it so easily.
My smutty romance book list - not part of the links, but figured I may as well share here. I love filthy explicitly detailed smutty romances. I'm also quite picky about what I like. If smutty romance is what you like, check out the link. Scifi, historical, historical fantasy, modern day/contemporary, and a mix of all of these are on the list.
Second, I have some details here for y'all since I know so many of you are a curious bunch...
I'm a Disabled queer artist with a focus on quilts. When able, I'm also a watercolor painter. My work is done Friday-Monday, taking Tuesday-Thursday off because those are my husband's days off. On those days, I game, write (mostly fanfiction), assist in housecleaning as my body allows, and spend time with Hubby.
I'm pagan and the pantheons I work with are Norse and Celtic. I'm a devotee of Cernunnos, and work a lot with Thor (patron god of the blue collar/working class), Freyja, and The Morrigan. Every home has spirits, and I've been working with those who reside in my own house. I love their company and it appears they enjoy mine as well. I do suggest you talk to your home, set up a little shrine with something as simple as a plant, a bowl, and a cup. Share a portion of your meals with them, explain changes you've made and why (like hanging artwork, home improvements, etc), and build a relationship with them. It makes a big difference. Call me crazy if you want, but it's spooked tf outta my husband when he saw how swiftly things improved when he apologized to the house and explained the home improvements and repairs we've made.
Some info regarding my style:
My style will never be called subtle. Bold and bright is my route. Even when working in black and white, I will make it stand out.
My personal aesthetic is cottage core, stained glass, art nouveau, and Hawaiian prints (especially the campy stuff).
I lean towards jewel-tones, which is why I really enjoy making stained glass quilts. Bright jewel-tones with the darkest black in strips between sections? Fuck, yes.
My favorite animals are housecats, snow leopards, clouded leopards, penguins, peacocks, and hummingbirds. In that order. The last two are the colorful ones.
My favorite flowers are daisies of every kind, and very fragrant flowers. Not a fan of roses though. I think they're overrated.
I collect teacups and fairies, with a big love for mushrooms, moss, and teapots.
Most of my quilts are small because they're quick to make. My primary focus has been on stocking my shop, but now that my husband has a well-paying job as a sous chef, I can focus on decorating our home and get to work on the quilts I wanna make for us.
We're turning what is technically the dining room into my quilting room. It's slow-going due to my disabilities, but it's coming along. The walls are no longer shiny hospital blue, but are a matte green and the ceiling a matte white. I've moved The Monster (my massive hutch) in there and will be painting it as well. the room with have The Monster to store all my tea-related stuff (I love tea), and everything related to machine quilting.
I have a machine quilting frame, and a domestic sewing machine specifically for it, set up in there for me to work on BIG quilts. They'll be put to use after the room is finished.
Fun facts:
We will be celebrating 20 years of marriage in 2026. Yay! We married at a renaissance fair in 2006, but the seizure med I was on at that time prevented me from developing many memories. I have flashes of the wedding, but that's it.
I'm epileptic and have seizures everyday. Thankfully, the Big Ones, in my case tonic-clonic, aren't daily.
I was diagnosed with hEDS when I was 41. My doctor genuinely believed I had been diagnosed already because the symptoms are so obvious. We've also come to the conclusion I have vEDS due to the severity and ease with which I bruise, the length of time it takes for bruises and injuries to heal, and various other interesting things. Unfortunately, the only way to officially diagnose vEDS is via genetics testing. My insurance won't cover it.
To make things more interesting, I have POTS as well. I get virtually no sewing done during the summer/dry season due to this. My sewing room gets hot as balls before noon due to where the room being on the more eastern side of the house. I have to get up at around 5AM in order to get anything done in there. Thankfully, it's only four months of hell. My tolerance for heat is almost comically low.
I've got other disabilities as well. These are why I cannot work a "Real Job." I do my best to bring in money via selling my work. Please, purchase my work. I know commissions and custom-made items are awesome, but they take time. There are many listings in my shop, with more incoming, and I can ship those off right away.
When I drop things, I, um...sorta scream? Not the sort that would scare anyone into thinking I'm dealing with a home invasion or violence. Let's just say that Telemed appointments have resulted in my doctors laughing themselves to tears because I dropped my pen on the floor or whatever. In person, this shit is so much funnier and absurd.
My husband is a DnD dungeon/game master, and his players have heard me scream like my previous point. It never fails to make everyone laugh.
He paints the miniatures he uses in his games, and I construct all the buildings. The only thing that stopped me from becoming a carpenter was my seizures. They and heavy operating equipment with sharp blades do not mix well at all.
Hubby is a professional cook. The only reason he doesn't call himself a chef is due to not going to cooking school. This man has been working in kitchens for more than 30 years. He is a fucking chef, and his own employer has said as much. It does make him grin every time I tell someone I have my own personal chef, though.
He is also my official caregiver and is even paid by the state. It covers our mortgage and a portion of our bills, and takes some of the guilt about being a burden off my mind. He refuses to say I'm a burden, and shushes me anytime I mention feeling guilty about being unable to bring in more money.
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The clinic i recently went to for the surgery-consultation-but-it-wasn't called this morning. They have an opening to see me and aspirate the cyst in...September.
That's more than a month. I would likely already be scheduled for hip surgery.
Well, i declined, and when they asked why...
...oh, i told her allllll about the horrible visit.
It was scheduled for 9:30am. It was nearly 11am when they finally called me back. When i asked why tf it took so long? "Computer problem" which is a bullshit excuse. Just say you're understaffed and over-scheduled. The nurse may have winced and nodded.
Sitting is extremely painful. It pinches the cyst and flap tear on the front of my hip. I stand in waiting rooms now...so long as i have a wall to lean against. The walls had chairs all along them. Nowhere to lean. I ended up sitting weirdly, leg stretch out, me trying to not pinch the spot. I arrived at a level 6/10 pain level. Left at nearly 9/10 pain level, and in tears.
I get tp the room, and told them i cannot sit, at all. They had my mri scan up and saw the mess. They knew and could see it. Still insist i try touch my toes while they poked around. My muscles were spasming because of how I had to sit. They spiked my pain up. A lot.
My hip sublexed the next day, which is a partial dislocation. I could feel my pelvis moving one way and the head of my femur in the other direction. Same setup as the dislocation that caused the tear. I couldn't put weight on that leg until i saw my PT four days after the appointment.
I mentioned the place to my husband's dnd players, and one of them knows the place. He's a skier and has had serious injuries. He told me they always have computer problems. His insurance wouldn't let him switch to a different clinic until he went this one thrice. First appointment of the day, at 8am? Pack lunch. Always a two hour wait. Crap quality treatment resulted in leaving with more problems. They treated him with virtually zero respect.
I looked up reviewd. How are they still in business? One star, sometimes two. They've been having this same "computer problem" for two years.
The woman on the phone took notes. She apologized, and said she's gonna check on the system to see if i was correct. Oh, and mentioned it sounds like the most accurate and likely culprit. Then she told me she's passing on what i said, that the people running the place may decide to take it seriously.
I left that clinic in tears, barely capable of walking. The only thing i can use for pain treatment is edibles. OTC pain meds and nearly all Rx pain meds make me vomit. Tylenol/acetamenaphin damages my liver and makes me extremely nauseated, which is why it's used only for breaking fevers. Morphine increases my pain. I'm completely immune to opiates. They may as well be candy for all the effect they have. Not even side effects. My mom and one of my sisters has the exact same experience with opiates.
My edibles make me unable to do much. I become very stupid, and extremely uncoordinated. My sewing room is dangerous, and moreso when the effects kick in. I wanna work on quilts, but edibles don't make that possible.
It's taken over a week for the spasms to calm down. Walking is getting easier, and i can put weight on my leg. I got some sewing done, which is great.
Hopefully, the place takes my complaint seriously.
This disability pride month I would like the community to understand that Sometimes wheelchairs aren’t freedom.
Sometimes using a wheelchair means you can no longer get to the places that used to be important to you, and not because of man-made inaccessibility. I have sat with someone as they cried because they could no longer visit the place they had scattered a loved one’s ashes because not even the most expensive wheelchair in the world could handle the terrain. As much as I wanted to, my wheelchair meant that I couldn’t position myself in a way that would allow me to give them a proper hug. In that moment, our wheelchairs felt more like heavy weights than freedom.
And sometimes wheelchairs are like the legs of someone who can walk but would maybe benefit from a wheelchair themselves. Sometimes wheelchairs are exhausting and painful and you’re counting down the time before you’re able to be lifted into bed. Sure, like painful legs, you can do more with them than without, but constantly performing gratitude for something that hurts you is exhausting. And again, not because you need a better wheelchair, but because those are the limits of your body and the technology that exists.
Yes it’s important to challenge the idea that wheelchairs are always a tragedy. And yes, there are lots of people who have a positive relationship with their chair. But for a lot of people, including me, the pressure to love your wheelchair and see it as freedom is painful and feels like it erases huge amounts of my experiences with disability.
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My hip surgery consultation did not go well. They were more middleman than anything else. It was basically confirmation i do need surgery. They sent a referral out for an orthopedic surgeon. In a month, i may hear from them again about apirating the cyst next to the flap tear, and a cortisol shot to reduce the swelling. The earliest they can see me is at the end of August.
I was hoping for surgery during the summer. The weather rarely changes, which has my joints happy. Autumn fluctuates and makes my body very unhappy.
In good news, i have plenty of time to finish the wallhanging i plan on hanging in my sewing room.
We're still preparing for my surgery, which means
prepping the house, and hopefully getting a ramp installed,
putting together activities to keep me occupied, like Lego sets,
and putting money together for me to get the laptop I need, seeing as I would like to write my book. Currently, i cannot sit at my computer because i end up pinching the injured area of my hip.
I have a list you can order from and help me out here. It has the laptop crowdfund, ttrpg constructs for me to build, Lego sets, food, postcards and postage stamps (i'm active on postcrossing), and various other things. You can order them on my behalf, with the option of remaining anonymous.
Commissions are open, with ten slots, and will remain open until all slots are taken or when the wet season arrives...so probably October.
If you would like to have something handmade and one-of-a-kind, check out my quilts. As small as 1.5x1.5 inches and as large as queen size.
I will work on commissions as much as I safely can. When surgery happens, there will be a lengthy wait. Could be a few weeks or a few months. Snatch up a slot soon!
Please reblog!!!
I'm on social security, and my husband hasn't been able to find a second job. What he makes as my state-paid caregiver covers our mortgage and a couple bills. My SSDI covers about two weeks of groceries and one other bill. Before our current leadership caused inflation to get this bad, it would have been barely enough. Not anymore. Any help we can get will make a difference, and that includes reblogging, which is free.
Liking a post bookmarks it for you, reblogs get seen.
please wear sunscreen!!! I've seen "fuck the beauty industrial complex" posts about complicated skincare regimens and am 100% with them except sometimes they mention sunscreen and no. no. absolutely not. sunscreen is a wonderful supportive friend who wants to keep you safe, and you should let her do it. throw out all your other cosmetics and skincare products if you want, but keep your sunscreen. and if you're not wearing sunscreen, start wearing it!!!! this is not about terror of aging, this is not about every tiny imperfection our fucked-up culture has made you feel insecure about, this is about protecting yourself from skin cancer. wear the damn sunscreen.
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Let's start a list of books/authors, games, TV shows/series, films, plays, and musicals featuring Disabled characters!
Battlestar Galactica (newer version) - PTSD all around, as well as characters with cancer, losing limbs, etc. It does an outstanding job showing these things in a way that makes it more realistic and grounded. It's a darker show and may be hard to watch for some, but it's also amazing. Disabled characters aren't treated like an accessory, but as a core part of the story.
Star Trek - mosr of the series have multiple Disabled characters. I can't watch anything beyond DS9 because it got too flashy and triggered my seizures. The irony...
Dragon Age - PTSD all around, but more pronounced in some characters more than others. Cullen has PTSD and lyrium addiction, all templars have lyrium addiction and the debilitating longterm effects. Leliana turned to being a Chantry sister to help recover from what caused her PTSD. Anders and Fenris do as well and are violent about expressing it. Cole is written as though he's autistic, which, if made fully human, he definitely is. Nearly all circle mages are traumatized by the way they're treated. Neve has a prosthetic leg, Bellara has ADHD, Lucanis has extreme PTSD. It's a lot, and though it may seem terrible to say, i love seeing this. It makes the characters more real.
Defying Doomsday - a book packed with shortstories, all of which are about Disabled characters experiencing an apocalypse
The Hunger Games - in the book, Pita loses his leg. Katniss was nearly deafened and needed ear surgery, PTSD across the board, multiple physical disabilities
Dune - the book series, not the film abominations.
The Wheel of Time - the book series, not the TV alternate universe fanfiction version.
Authors i enjoy reading who include Disabled characters. In fact, many of them have their main characters written as Disabled:
Ann Aquirre
Kevin J Anderson
Mark Chadbourn
Joy Demorra aka @thebibliosphere
NK Jemisin
Chloe Liese
Lyonne Riley
Brandon Sanderson
Nalini Singh
Reblog and please, include additions if you have any!
Seeing people try to defend the lack of racial/ethnic diversity on Tumblr is... wow. So let me share a reminder: It used to be better! Still dominantly white, but better than what it is now, at least. Then everyone got tired of the "blackouts" and other mostly Black-led conversations around racism because it was "ruining their fandom fun" or something idk and quite literally chased out so many bloggers of colour through harassment campaigns from the user-base and massive staff-led blog purges. This was not even that long ago, btw.
I can think of so many beloved mutuals who had to leave this site for their mental health because they just couldn't take it anymore.
Tumblr deserves every shred of criticism it gets for being so white after all that.
*tap tap* Is this thing on??? I had to reset my password to get back on here after all these years. It's me, the #BlackoutDay co-creator formerly known as blackoutqueen.
OP and the folks in the comments -- I have to say I am honored that people still remember and hold #BlackoutDay dear to their hearts a whole ten years later. It makes me happy that those days are remembered fondly. When a dear friend of mine told me this post was going around, I figured I should pop back on and say a bit of my piece.
You're right. This site deserves every bit of criticism it gets for how it centers and upholds whiteness.
For years, I tried to be strong and tried to be polite as I got bombarded from every side -- slurs and threats of doxxing from racists, misdirected anger from Black bloggers who felt hurt they never went viral, snide remarks from people on Black Twitter who felt ownership over #BlackoutDay because apparently Black Twitter was the only subculture with any impact online, doxxing from misogynistic YouTubers like Tommy Sotomayer, whining fandoms, staff and Tumblr as a brand featuring us and then leaving us to the wolves whenever we got harrassed, and tbh, a co-creator of mine who almost always needed reminding to treat the younger women around him (including me) with respect. Between all that and people calling me selfish for wanting to be cited and credited correctly, I gave up.
I was only 20 when #BlackoutDay started, and when it all became too much, I decided to put myself first and give up on organizing it all together. I left Tumblr and don't usually talk about #BlackoutDay anymore because for the incredible impact I made across the internet, I only earned suffering. To this day, the mention of it really breaks my heart because I saw so much potential for us that I literally changed my career to pursue that dream, and racism, fatphobia, and anti-Blackness shattered it to bits.
I'm doing okay these days, using the skills I crafted here as a young person to organize IRL, but have all but stopped mentioning my involvement in #BlackoutDay simply because remembering how that was the start of people treating me like garbage on Tumblr, a site I was giving my heart to and working on changing for free, still gives me chills in the worst way. The staff at the time knew how I was being hurt and did nothing, my mutuals were breaking their fingers trying to defend me, and it was too much.
I hope you all who still actively use Tumblr know that despite everything, you still have the power to change the culture of this site. Given all the things we are currently witnessing (Free Palestine, the Congo, Sudan, until we are all free), you can make little changes and stand for what is honest and true, and you don't need special days to do it.
I thank everyone who ever participated and boosted #BlackoutDay from the bottom of my heart.
I wish you all a very nice weekend with a soft morning kiss between Hawke and Fenris ! I was like coming home, drawing them again so I hope you'll like the drawing !
The joy of finding an old forgotten WIP in my files haha ! Fenhawke will still have the place n°1 in my heart ! ♡
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It was a huge milestone of scientific and technological advancement. (Plus, at the time, politically significant). Humanity went to space! We set foot on a celestial body that was not earth for the first time in human history! That’s a big deal! I’ve never thought about it before but now that I have, it’s ridiculous to me that that’s not part of our everyday lives and the public consciousness anymore. Why don’t we have a public holiday and a family barbecue about it. Why have I never seen the original broadcast of the moon landing? It should be all over the news every year!
It’s July 20th. That’s the day of the moon landing. Next year is going to be the 54th anniversary. I’m ordering astronaut shaped cookie cutters on Etsy and I’m going to have a goddamn potluck. You’re all invited.
PITCH: We call it Moon Day, and then every 7 years when it falls on a Monday, that's an even BIGGER deal and we call that Moon Day Monday and go absolutely apeshit about it (the next Moon Day Monday is in 2026 so we have a couple trial runs first)