#crowdsourcing

[reasonsforhope]

Happy Holidays to everyone celebrating holidays right now!!

Let's spread some holiday cheer and crowdsource this shit!

Link a good news story that you know in the notes on this post!

--

Here's mine, I'm cheating by providing a giant compilation that is by FAR the best good news roundup I've seen this year.

-via Fix the News, December 19, 2024

And for those of your who have already seen that from my other post, here's another great compilation!

-via Positive.News, December 23, 2024

[digitalnewberry]

How's your cursive?

William Ellen Wallace whaling logbook, 1841-1844 (view | transcribe)

Newberry Transcribe -- our crowdsourcing site where you can help with historical research by transcribing handwritten letters and diaries -- is back in action!

From screenwriters to socialists to soldiers, the subjects of our collections left behind a wealth of primary source materials -- such as the above 1840s whaling logbook that includes what some of us thought were whimsical doodles, but turned out to be a much less fun industry convention indicating "how many gallons of oil were procured from each [whale] body."

Libraries lack sufficient staff to transcribe the millions of manuscript pages in our collections, so it used to be up to the user to painstakingly decipher every page, with each individual replicating this work from scratch. Thanks to the magic of crowdsourcing, the public can volunteer to help out by transcribing the page once and for all, allowing researchers to easily find, search, and browse the material.

Plus, figuring out the handwriting can be a fun challenge. Wordle, shmordle -- come solve puzzles while also learning about history and contributing to humanities research!

Visit Newberry Transcribe

Read our project newsletter

Jack Conroy correspondence at Newberry Transcribe

[why-animals-do-the-thing]

I’ve got some accessibility questions around zoo maps! Specifically, I’m interested in how people are impacted by the lack of paper maps / digitization of maps, especially when the ones in other languages than English are only online.

Please chime in in the replies and tell me about accessibility impacts you’ve experienced (or know someone who has experience) with:

No paper map policies

Online-only maps

QR codes to access maps

Maps available in an app only

Policies that instruct visitors to print their own maps ahead of time at home

Being told to photograph big signs with maps on them throughout the zoo in lieu of using an online map

Non-English maps being available online only

Policies that guests should use an app / Google translate to access map information / signage

I’ve got my own thoughts, but I know my perspective is limited to my personal experience. If these policies impact you in any way - not just due to disability - please tell me how. TIA!

[femmepeterparker]

hello!

i hate to beg but i was in a car accident on sunday night and now have to pay to fix my car ($249), rent a car ($50 + $40 a day for as long as i need it), and pay a citation (unspecified amount because they haven't added my ticket into the system.) i am also currently struggling with my health and have several doctor's appointments lined up that will probably range between $100 and $200. if anyone can help, it would be greatly appreciated. thank you!

cash@pp: $horatiobo

payp@l: please send a message for my @

[weaselmcdiesel]

Want to help me with an assignment by talking about your pet?

Hi!! I have an assignment to make a piece of art using crowdsourcing. My idea involves collecting a lot of text about people's pets! Anything about them, what you like about them, a description of their personality or appearance, something funny they did--really anything. In the end, I want to use all the text to make something interesting (I haven't decided the specifics yet). I'll upload the finished project here when it's done! (it's due a week from now, March 12th)

How to be a part of this project:

Reply to this post or reblog and put in the tags or in the post itself anything you want about your pet. You can also send me an ask if you want, but I will not post any of these asks.

If you want to speak about a pet that has passed, please indicate somewhere in your reply that it has passed. I intend to use that information in the piece itself.

You can include a picture of your pet ONLY IF YOU WANT! Pictures aren't necessary but I might figure out a way to incorporate them.

Important:

The text you provide is not going to be credited to you/your url, everything will be anonymous.

I'll be reblogging this every now and then to help get a lot of different responses :) Sorry if you get sick of seeing this post! Also, if you don't have a pet or you don't want to talk about your pet, it would help out if you would reblog this anyway! But ofc, you don't have to.

[patmax17]

Looking for ttrpg suggestions: character focused and with a bit of crunch!

Hi tumblr! I want to try to crowdsource, like opening my mind to the psychic maelstrom.

The kind of stories I like most are character focused, where they face hard choices that challenge their beliefs and values, and where they have to learn from their mistakes and the consequences of their actions. Bonus points if friendship is important!

I also like crunchy games with combat, I like finding combos and feeling smart about the use of my skills, as well as cooperating with my teammates.

On the "role-playing side", I like game systems that help the players (and DM) set up a stage loaded with potentials, and give inputs about what could happen next.

Games i like are:

Dogs in the Vineyard: I love the way building the town gives the GM a tense situation with NPCs that have clear agendas, the conflict resolution mechanic gives hard choices to the players, and the experience mechanic really gives a sense of how the characters grow based on their choices and the consequences of those choices (writing this now I see how DitV actually hits all the sweet spots for me)

In Contenders I like how it has an internal economy of currencies, and the state of each currency guides the kind of scene you want to play

Kagematsu is very simple but incredibly elegant in its design, I especially like the mechanic of the acts of desperation, and how they interact with how you earn love

Apocalypse World is character focused, it doesn't have a party but follows a cast of character with intertwined stories

Atlas:Reckoning never saw the light of day, but I liked how it was the right amount of crunchy, how the "drift" mechanic helped explore the pilots' backsyory and deeper layers, and how the out-of-combat scenes were structured in a similar way to Contenders

I've been ootl of recent ttrpg games in the last years (mainly because I don't have a stable playing group anymore). So here I am, asking for suggestions to all tumblr ttrpg connoisseurs out there.

Thanks!

[datvtranscripts]

does uh. anyone want to record the fade memories from a playthrough where you don't do the labs below memory first. for science.

[deebrisbyfish]

In wrapping up the crossover, I decided to have a little 4th wall-breaking fun. "Finding Dee" actually began with me, as "the cartoonist" coming out as Trans IN a "Dandy & Company" strip. That makes this comic, technically, a spin-off. I had been a recurring character in the strip for YEARS and had a regularly tense relationship with my own creations. It seemed fitting to end this crossover with my having fun with that dynamic and reasserting that this is taking place slightly outside the "reality" of the regular strip.

[greaterblogston]

Happy Monday party people.

Ollie Morris nd I just finalized a track on The Perfect Sentence that is so beautiful and I can't wait for people to hear it.

Just a reminder that I'm still pushing the TPS Indiegogo. Click the link to learn more and contribute if you can.

Also - were at 76%. Amazing. My goal is to hit 80% by Wednesday and we only need $77 to get there.

[leiascully]

Hi there Leiascully! I was directed your way by Fanfic Reddit hoping you might be able to point me in the direction of an old, old Xfiles fic that might still be on Gossamer.

The premise of this fic was kind of Pusher-esque in that there was a villain who had the ability to - with a bare hand - touch you and in an instant learn all of your secrets, your background details, your heart's desires. I'm 99% sure he laid a hand on both Scully and Mulder, separately. And this villain had captured Scully, and was holding her at knife point. In the climax, the villain was in a standoff between himself and Mulder and forced Mulder to admit that he loved Scully - just to toy with him before he killed them both. Then Scully jumped into action (I think she kicked the guy in the crotch) and ducked, getting injured by a knife slash while Mulder shot the guy dead.

(There was also a sequel where Scully had The Talk with Mulder afterwards about whether or not he meant it)

Does this ring a bell? It's been a while since I've read it - its probably my favorite, and Im kinda dying to re-read it.

Bless fanfic reddit for their faith in me, but I am not the best fic reccer! That's @lilydalexf or @randomfoggytiger or @calimanc - they've all kept much better records than I have! I'll poke around, but they might already know :) It sounds great!

[digitalnewberry]

Say you're an artist...

... but you have a day job, so you take an evening class at the Art Institute, but it's the early 1890s which is pre-indoor lighting technology, so you can't draw the human figure from live models. What would you do??

That's right -- you'd probably start a Sunday morning art class just down the street from the Newberry, and call it the Palette & Chisel Club. And now, 130ish years later, we're both still going strong -- they continue to teach art classes, we're digitizing their archives and adding handwritten items to Newberry Transcribe, our transcription crowdsourcing site. So please stop by and browse their first scrapbook (1895-1906) at our digital collections site, or transcribe it to create searchable text documenting drunken art student shenanigans Chicago's early art scene.

[why-animals-do-the-thing]

Okay, this is super preliminary, but since we've been talking about zoo accessibility I wanted to launch a project I've been planning for a couple months.

One of the hardest things about visiting zoological facilities when disabled is the lack of knowledge ahead of time, right? Often the information on the zoo's website about accessibility doesn't contain everything folk need to know to plan a visit. I think we can probably help fix that, even if it's with just crowd-sourced knowledge!

This is a google spreadsheet for recording accessibility information for various zoos. It is super unfinished right now, FYI. That's partially because I need to fill in more of it from my own experiences, and partially because there are things I didn't note or experience - which I'd love for y'all to chime in about.

Categories for the spreadsheet so far include rentable assistance options, service dog information, accessible bathroom locations, mobility, vision, auditory and sensory issues (or accommodations), food allergy options, and general notes. I'm also including the information each zoo website provides, and guest assistance phone numbers, so all the information is in one place.

To add to this crowd-sourced zoo accessibility resource:

Send an ask to the blog, or comment on the appropriate cel on the spreadsheet (if the facility you want to comment on is already listed).

Provide the name of the zoo/aquarium/sanctuary and the approximate date you visited.

Tell me your experiences / information, and what categories they belong in.

Feel free to submit photos, if that's useful info! I'm going to see if I can find a way to host them and link in the spreadsheet.

I'll take information as it's submitted and integrate it into the sheet. If the zoo you've visited isn't on the list yet, I still want to add it! This resource is going to stay US-based, however. (I just don't have the capacity to manage an international one).

Obviously, I can't personally verify everything people submit, so this is very much a resource and not a definitive guide. Date stamps are crucial important for keeping track of what's recent and what might have been updated since someone visited.

Let's make zoo, aquarium, and sanctuary visits more accessible for everyone!

[deliciouskeys]

Related question: who has used the term 'supe' in the show?

Butcher obviously. Frenchie, MM, and I think Hughie from time to time. I think Grace Mallory has. Bob Singer. Joe Kessler (lol).

Has Annie? Did Becca?

Has any supe or anyone employed by Vought ever used it?

Control F-ing some scripts, Sage did refer to herself as a supe on at least one occasion, and in Season 4 'Supe' seems to have acquired a new connotation. Firecracker is introduced as "a leading voice of the alt-Supe movement on YouTube". But it seems to be a term Vought has been staying away from using?

[scretladyspider]

please don’t scroll; I really need your help to reach my gofundme goal of $3500 and not become homeless.

Im Elle, a queer, ace, disabled person with ADHD, depression, and two cats. In November, I lost my job without warning. I have no savings as the job already had me living to the last dollar of every paycheck. I was denied unemployment and food stamps. I cannot work away from home, a physical job, or something with strict hours due to some yet-to-be-diagnosed illness.

this is my story — what’s going on & how I got here. (Smaller text used because it’s a lot of information/a long post.)

In early 2018, I was doing regular walk/runs. In 2019, I stopped being able to run, so I went on walks. Running took hours, then days, to recover from. My body couldn’t produce energy to do it consistently, so, walks. In 2020, I kept going on walks and tried to do aerobics. I was not able to keep doing aerobics. My body took hours upon hours to recover, where before it hadn’t, I was alone for almost all of 2020, and never developed COVID symptoms; it was what happened with running all over again. In 2021, it started to take more time to recover from walks. Then I started to need to take a nap immediately after I clocked out from work— and it was a work from home job. In 2022, I began to go from my sitting desk job straight to my bed most days, laying down exhausted right after work, even sleeping through lunch to get some rest.

On New Year's Eve 2023, I spent 30 minutes cleaning, including vacuuming my living room. I had to rest the rest of the day.

In the last five years, I've gone from running to being exhausted for hours by taking my garbage to the curb.

Imagine you were someone who enjoyed recreational exercise. Now imagine doing 1/100th of that and feeling sick for days. Thats me.

There are other symptoms also. More vulnerability to infection and more trouble fighting infection. Shooting, sharp muscle pains in large muscles such as the thigh or forearm, like a pinched nerve, that come and go at random. Pulse rate that skyrockets upon standing, to go back to normal soon after. Stomach inflammation. Inflammation without major swelling. Headaches. Complete inability to tolerate heat, leading to excruciating migraines that only go away with things like cold showers, electrolytes, and hours of rest in the dark with ice. Muscles that literally don't feel like they're getting oxygen. Random rashes. Face flushing. Being much more easily out of breath, yawning over and over, like I can't get air correctly. Weight gain, no matter what I eat or don't eat.

And just being so, so tired.

In summer of 2018, something… stopped working in my body. I felt sick all the time. I had a low, unexplainable fever nearly every day. Shooting nerve pain would wake me up at night. The doctor said I had a cold. But months went by and I didn’t get better. When my blood work and thyroid hormone level was normal, I was referred to a rheumatologist.

I was diagnosed with fibromyalgia after he made me wait 45 minutes, came in and asked “are you tired?", poked me hard, said I was tender, and left without running tests. This sort of “uhm the standard blood work came back normal, have you tried exercising more? I know you’re here because your body can’t recover from it but have you tried more of that? Also going to sleep at night?” has been the response over and over and over for five years. It got to the point where I even started to wonder if I was somehow making it up. I see a psych nurse. She thinks there's more than just depression, ADHD, and other things - though we both agree that managing those is vital too. She used to be a cardiologist, so this is reassuring. But when I have tried to see other doctors, it goes differently. Most of the time they see I have ADHD, a long history of depression, and hypermobile joints, and say that explains everything. I can't count how many times I've been told "well, you have depression” when the labs, if they even agreed to run them, came back normal. My standard blood work sometimes comes back with anemia, but I take an iron supplement. No improvement had come of it. I’ve had my thyroid hormone levels tested over and over, but never the antibodies. No imaging or referrals have happened, outside of one to a second rheumatologist. He ran no tests either; he just saw my joints are hypermobile and I was “sure taking a lot of mental health medications” (two at the time), and… that was that.

I had given up on actually even getting help until my SIL recommended a doctor she knew. For the first time in five years, when the standard blood work and TSH tests were normal, she told me we would keep looking. I actually cried with relief at that. It’s amazing to be believed after all this time.

Because of …. All of this, I'm trying to figure out how to either work for myself or find a work from home job that has flexible hours I can choose. I literally wouldn't be able to work a retail gig where I have to stand for eight hours, or even a 9-5 where I have to be there for those exact hours, because my body cannot do that right now. I want to get better but it's a long way off. First I need to know what's even wrong. I'm praying for a diagnosis soon. And treatment. At the least, management.

I have heard of EDS and I have been evaluated. I apparently don’t meet enough criteria, hence the diagnosis of JHS instead. It’s in the same family. I have also heard of POTS. I am pursuing testing. Same with Chronic Fatigue Syndrome, MCAS, fibromyalgia… yeah. The thing is nothing outside of the standard blood count and thyroid hormone level test, no other lab tests have been done. There are so many things this could be that have never been checked. Lyme disease, for example, is extremely common where I live (it’s actually just extremely common worldwide) and matches much of my experience, but 1) in the USA the initial Lyme test relies on a strain of bacteria cultured in the 80s 2) there are over 100 strains of Lyme disease in the USA 3) in spite of decades of research there are doctors who don’t believe chronic Lyme exists 4) no doctor has ever checked and I only recently learned anything about it so I never asked. But… there are a lot of things to check that I’ve never had checked is my point. Fingers crossed someone can help me get there.

I do not have a partner who can try to support me through this, and my family already supports me however they can. My severance (which was low as I found out I was being paid much less than the rest of the team later) paid only my January rent.

Since my ability to work is severely limited right now, and I've been denied unemployment and food stamps, and I would need a diagnosis and to be awarded disability benefits in court (which can take YEARS that I don’t have), I have nothing in savings because of years of underpaying jobs the cost of living and being disabled and going through prior periods of unemployment due to this and other factors, I am left in a tough spot without help. Without this help, this gofundme... I have nothing.

So... here I am. A queer nonbinary disabled neurodivergent writer, trying my best, living with some undiagnosed illness that's severely impacted my ability to function, who got fired without real reasons (in America they can just do that to you without even telling you why), asking for your help to pay my February rent and January bills so I don’t repeat the trauma of being homeless. Or for you to reblog this.

Thank you for reading all of this.

It’s been on my chest for a long time. Even if it wasn’t for the gofundme, it feels good to talk about and be honest about my health. It reminds me you’re not supposed to feel like this all the time when I tell other people and they tell me I should get help and deserve answers. It’s reassuring to see competent doctors who finally believe me. I hope we figure it out.

no donation is too small— they add up. If just 100 people gave $35, the goal would be met. Sharing is also giving— it means someone who can help is more likely to see it.

You can also help via my venmo — secretladyspider

CashApp — secretladyspider

or find PayPal in my tip jar in my linktree

Goal is $3500 or over. Funds needed ASAP. If it goes over, that’ll help with February.

Thank you for anything and everything.

[quidam-vir]

The Latin Collaborative & Creative Internet

Welcome to my little reference post! I love all the crowd sourced places and places of creative expression on the Internet. I especially love when small communities, like Latin speakers, come together and do cool things. I want to shout-out some of these Latin-specific projects and places just to spread possibilities for the wide-reaching īnsolitī hominēs around the globe. Grow community resources, express yourself or have something fun to do if you're bored.

1. Software Translations (Launchpad)

Over at launchpad they crowdsource translations for a bunch of open source software. Think of your favorite open source software and chances are it'll be on there and you could help make a Latin version. Applications range from Blender to Chromium to Ubuntu to a Dice Roller or Tetris clone

I have the dream of assembling a team of good Latin translators to complete the translation of Linux Mint and help create the first major operating system entirely in Latin.

2. Victionarium

Love Wiktionary? I know I do. How about Wiktionary in Latin? Create definitions and dictionary entries for Latin words, in Latin. The more it's built up, the better this resource would be for learning new words.

Helping add Latin words or forms to the English Wiktionary is also helpful, sed scīlicet the Latin one needs in more.

3. Vicipaedia

Another Wikimedia project, who could've guessed? The Latin Wikipedia, Vicipaedia, is another great resource and one that could use more contributors. If you are knowledgeable, willing to learn, and good at Latin writing, try it out!

4. LibriVox

Are you one of the few that enjoy and are confident speaking Latin? Even if you're not, practice makes perfect! LibriVox is well known for a host of free audiobooks, and this includes ones in Latin. They could certainly use more volunteers for the language, no matter which pronunciation system or cadence you prefer.

Places with a 'Latin' Post Setting

There are a few places you can write or post where you specifically can mark a post as being in Latin, and filter accordingly. Any I run across will be put below

1. AO3

Not a huge surprise—unlike the 99 currently existing Latin fics.

2. BlueSky

The Twitter clone from a while back has a language search and select with Latin (and some other old languages too)

If anyone has anymore places/projects to add, subtus narrā mihi!

[gutwrenchflowerbomb]

Do you buy handmade fan merch? Do you like wrestling? Wanna help me decide what to make next?

A while ago, I made this lil guy for myself using printed shrink plastic. It’s a pin!

I still have a ton of shrink plastic and pin backs. I know I’ve only offered stickers in my ko-fi shop so far, but I’d like to start branching out. What do y’all think would make a fun pin that you’d potentially buy?

I found this file in my iPad and I don’t remember where I was going with it (I also have all of the BCC and a few ladies done this way hahaha) but they could work as pins maybe?

Anyway, let me know in the comments or my messages! I appreciate it!