slowlymadeart
Evidence of Efforts Through Visual Mediums
Rachel Wann // A Spoonie's Art Blog //
Creator of "Slowly Made Comic"
The comics is also available on Webtoons, Instagram and facebook.
but let's be honest, tumblr is where the real snazz happens.
none-the-less,
This comic looks so much better on Webtoons. you can find it in the Discovery section under the title "Slowly Made Comic"
.....But here's the insta just in case. @slowlymadecomic
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Midwest Award for Artists with Disabilities
(5 Days left to submit work)
(I totally forgot to post about this sooner. My apologies. If you know any Artist with Disabilities in the midwest USA, send this their way!!! It's going to reoccur in 2024 and 2025. I don't have any connection with ArtsMidwest, just wanted to put the info here for others.)
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Source
Submission Deadline: May 22, 2023
Award Info: $3,000
Type: Grants & Fellowships
Eligibility: Regional; Illinois, Indiana, Iowa, Michigan, Minnesota, North Dakota, Ohio, South Dakota, Wisconsin, and the Native Nations that share this geography.
Categories: Craft/Traditional Arts, Photography, Drawing, Film/Video/New Media, Mixed-Media/Multi-Discipline, Painting, Sculpture
Description:
Arts Midwest is now accepting applications for the Midwest Award for Artists with Disabilities, an award supporting accessibility in the arts and celebrating the work of disabled Midwestern visual artists.
The Midwest Award for Artists with Disabilities supports and celebrates accessibility in the arts. It recognizes that the funding community in the Midwest has not historically invested in disabled artists and that increasing support for this group is an important part of increasing accessibility in the arts. It also advocates for the arts being viable employment, which is often overlooked by funding agencies supporting people with disabilities.
There are no requirements for how awarded funds are used, though awardees are encouraged to use it toward growing their art career. Awardees’ submitted work will be featured on the Arts Midwest website.
From 2023–2025, this award will recognize 27 individuals (9 per year).
Eligibility Info:
We invite mid-career 2D and 3D visual artists with disabilities to apply for this award.
You can apply and get (way) more info on the ArtsMidwest website here
#artistwithdisabilities#chronic illness#disabled#disabled artist#artgrants#artist#disability#disability rights#art help#spoonie artist#midwest#artsmidwest
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(Taken from this LightHouse article)
"The goal of this mission is to bring together the largest and most diverse group of disabled crew members in a weightless environment, with the hopes to learn how to adapt and make accessible outer-space travel for disabled space explorers, scientists, and researchers. The Mission: AstroAccess parabolic flight is scheduled to take place on October 17, 2021, launching from Long Beach, California.
“Our mission is to change outer space and change the world. If you are a disabled person who is confident, enthusiastic, playful, and literally willing to float upside down to change the future, we are looking for you!” says Dr. Sheri Wells-Jensen, Associate Professor of Linguistics at Bowling Green State University."
There is an impressive team behind AstroAccess, you can find the full list on their site here .
Here's a couple of those bios.
"Anna Voelker is the founder and Executive Director of the SciAccess Initiative, an international program dedicated to advancing disability inclusion in STEM. Through SciAccess, they lead numerous science inclusion initiatives, including an annual conference launched by their receipt of the 2018 Ohio State University President’s Prize. Anna specializes in accessible space science outreach for diverse learners and has worked extensively with blind and low vision students using 3D printing and data sonification. In June of 2021, Anna joined the Aspen Science Center as its new Executive Director. Anna is a 2018 Brooke Owens Fellow and previously worked at NASA Kennedy, NASA Goddard, the Space Telescope Science Institute, the International Astronomical Union’s Office of Astronomy for Development, and the Aerospace Corporation."
"Eric Ingram is the Founder and CEO of SCOUT Inc., a company de-risking space operations with sensor suites that enable spacecraft to see and understand the area around them. He also currently serves on the Board of Directors for the Space Frontier Foundation. He was previously an Aerospace Engineer for the Licensing and Evaluation Division of the FAA’s Office of Commercial Space Transportation, where he gained expertise in the regulatory environment. Prior to this, Eric was an engineer for Deep Space Industries, where he designed cubesat subsystems for testbed missions. Outside of the space industry, Eric previously served as the President of the United States Wheelchair Rugby Association, leading the USWRA to its largest budget surplus in its 30+ year history. Eric has competed in the sport of wheelchair rugby for 15+ years, competing domestically for several club teams, and internationally with the US Developmental team. Eric holds a Bachelor of Science in Physics from Old Dominion University, most of a Master of Science in Electrical Engineering from the University of Houston, a sport pilot certificate, and is working towards SCUBA certification."
"Dr. Sheri Wells-Jensen is an associate professor of linguistics at Bowling Green State University in Bowling Green, Ohio. Along with various aspects of astrobiology, her research interests include social aspects of human colonization, disability, the relationship between language, embodiment and thought, language evolution and ways in which alternative sensory inputs could influence the evolution of scientific thought. She is on the board of SOCIA (Social and Conceptual Issues in Astrobiology and METI (Messaging Extraterrestrial Intelligence) International."
"Dr Jamie L. Molaro is the Executive Director of Disabled for Accessibility in Space (DIAS). Dr. Molaro is a planetary scientist at the Planetary Science Institute and located geographically with host institution the Caltech/Jet Propulsion Laboratory. Her research focuses on understanding the way that rocky and icy materials fracture and break down, driving landscape evolution on asteroids, comets, and moons. She is also a team member on NASA’s OSIRIS-REx mission to retrieve a sample of rock from an asteroid surface. Service is an integral part of Molaro’s career, including organizing and running exhibitions and workshops on science and data-driven art, and leading DAIS (Disabled for Accessibility in Space). DAIS is a peer networking, support, and advocacy group for disabled and chronically ill people in space science and related fields and professions, and proud collaborator in Mission: AstroAccess."
Disabled… in SPACE!
Was perusing file770 a nerdy news aggregator and found this⤵️ announcement
so spread the word they’re looking for disabled applicants to ride a Vomit Comet,
did the preliminary research, it does not appear to be a scam, the parent organization SciAccess grew out of conversations at scientific conferences about equity and inclusion in STEM. Both ZERO-G social media pages have confirmed the partnership
MIT has been conducting annual flights of 50 students with the same company, ZERO-G, out of Fort Lauderdale, since 2016 (the link gives an idea of what experiments are like.)
#stem#astronomy#citizen science#accessibility#disability#transportation studies#accessible design#physical disability#actually disabled#diversity in stem#physically disabled#visually impaired#chronic illness#chronic disease#limited mobility#disabled community#signal boost#gotta get this out for the morning rush#wheelchair user#disability pride month#mobility aid#asl#stemblr#astroaccess#disabledspace
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Had to leave the apartment (for the 1st time in 2...possibly 3 months) for an appointment
and guess
what I got to see
(Exactly the same thing OP saw... OP just got much better photos, lol)
Y'all sit down because imma tell you about this wild story that happened in my hometown
So this local artist got paid real good money by the "owner" of this building to paint this custom mural on the side of his building. So he did and this is the end result (I'll get to the white paint on it in a sec)
Flash forward to like a few days later and the artist gets a call from the real owner of the building who came back from vacation to see this painted on the side of his building and is like the fuck did you paint on my building, so the artist says um you hired me to paint this? And the owner gets hella mad and in the end just hangs up because what else is he gonna do. The artist is just confused as hell because he thought he did a good job and that it's what his client wanted. Plus he got his money so he's left with these feelings of what the fuck just happened.
Meanwhile this shit has gained a cult following so when the owner eventually paints over it in white people lose their shit and protest, even bringing things to leave there like flowers and posters and make frequent pilgrimages there. However, since the painters didn't use the right paint the mural comes back due to rain/snow exposure, as pictured here.
I told my husband the story and we were just driving around the city today so we went and checked it out. We didn't stop so I just got a couple pictures of it while we drove by. Still glad I got to see this legendary piece of such a bizarre story.
The artist has tried to get in contact with the fake artist (he even met him in person before painting the mural) but no luck so I'm really hoping this person reveals themselves eventually. In the mean time, the owner has decided to paint a replacement mural more fitting for the city and tried to make amends with the artist after their initial heated conversation. So I'm eager to see what happens next with this crazy tale.
Link to the story, this is 100% true:
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I. DID.
I wanted to say something when I learned about this, but figured anyone who saw me post anything on the subject- forgot I posted anything.
This is awesome though. (I can't eat a bunch of these ingredients, but still, there are so many helpful things).
I feel a sense of duty to report that she appears to be kicking some serious ass.
(just checked out her website).
Katie Pennick is a disability campaigner, journalist and broadcaster based in London, UK (Totally pulled that from her website ) She's currently host of a podcast called/for the organization, Transport for All , a podcast to explore and raise awareness on disability and public transit.
“As a disabled person, you don’t have anyone to look to or learn from and no one hands you a book and says, ‘This is how you do things,’…You just have to figure things out and I worry that a lot of disabled people probably think they can’t cook"
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instagram
I know I haven't been posting much due to health and anxiety, but my partner, Billy Billiam Billocelot, made this insta account (purely for fun) for our newest guinea Pig, Shepard. (Sheppity Shep-Shep McSheppers).
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#image described#art#chronic pain#chronic illness#abled friends tag#disability#spoonie#mentel health#comic#disability art
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"You're Not Useless" [CC]
youtube
#jessica kellgren fozard#disability#Youarenotuseless#chronic illness#mental health#useless#you are not useless#hopeful#productively#ableism#internalized ableism#worth sharing#feeling worthless#chronic fatigue#this is the best#lovely people#she nailed it#Youtube
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Do you still exist, Rachel? And, if so, should reach out to your old friend, Colin. He misses you quite a lot.
*peers out from a rip in the pocket universe I've been hiding out in*
...Yeah....
Maybe it's time.
Tell Colin he'll have to wait! As I have many messages I've been too socially anxious to open, and now there's a que.
Wait. No. What am I saying?
I'm not ready for online human interaction, or any human interaction. I don't *starts to stammer* even....have a.... *sniffs the air and catches the scent of some very fine bullshit* have a WAY. OUT.... OF MY POCKET UNIVERSE!
Can't just...walk through the rip.
......It's....
................dangerous¿¿
What am I saying, characters use rips all the time to travel. That's how all the bad things in a sizable portion of shows infiltrate. So many things have escaped through rips.
Waiitttt, okay, so by tv show logic- either you, the world, need me trapped in this pocket universe, or I need to keep away from all of humanity . (Or I need to reside within the the universe with the rip, in order to support your main story line).
.....Well....
It's decided.
I'm fixing the rip.
Think'n it's for the best.
Don't know when I'll be done. Could be a minute to a month to a year....10.
Probably don't expect to much communication over this period time, as I will be very devoted to these efforts toward possibly saving all of our lives. That said communication will continue to be available, but between the fixing the rip and my pathological social avoidance, eh.
But hold hope! Because though I am defeated, afraid, and I can't draw because of migraines that happen because of neck problems-
-I also guilt myself relentlessly, especially with things like inconvincing people, not responding to messages, or not being able to feel I have anything to offer them. I needlessly become terrified of failing people. I can't remain okay enough to handle the anxiety that comes with being vulnerable. I Take one shower every 8 days, and some days are not the days when I can barely speak.
(I wrote that genuinely thinking it would come out positive when done, but that is not at all where it went. Oh my God, Ahha. Aahhhhahaha. Hoo boy).
But hey! People are nice and found families and are out there waiting to be found.
*confident nod*!
2020! Gonna get through it!
Barely.
*looks at you before disapearing into the universe behind the rip*
Tell Colin.
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https://www.healthrising.org/blog/2019/05/21/jennifer-brea-chronic-fatigue-mecfs-recovering-story/
"There’s no doubt this is not the easy way out for ME/CFS. If I could choose a way to recover – which I obviously can’t – neurosurgery would be one of the last options on my list. I think I would rather swallow a toxic chemotherapy drug than have a neurosurgeon fuse my head to the top of my spinal column. That procedure sounds about as spine-tinglingly scary as anything I can imagine. (Brain surgery would probably be worse.) The fact that only four neurosurgeons in the world can be trusted to do this procedure doesn’t help.
Among the first thoughts I had upon learning of Jen’s recovery was that if this is what it takes – a rare diagnosis and neurosurgery – if that’s what it really takes to recover, I don’t know that that’s ever going to happen.
After some reflection, I don’t think it’s as bad as that. Jeff and Jen and two other people have found a way and a remarkable 20 people on Phoenix RIsing have gotten a diagnosis. While getting a diagnosis isn’t a piece of cake, it can and is being done."
"Jeff and Jen’s stories do bring a new focus to the spine and brainstem. Hip, on the Phoenix Rising Forums, pointed to five structural conditions which can cause brain stem or spinal cord compression – and ME/CFS-like symptoms:
cervical spinal stenosis — spinal canal becomes too narrow, which can put pressure on the nerves
syringomyelia — fluid-filled cyst in the spinal cord which compresses the spinal nerves
Chiari malformation — where brain tissue is pushed into the spinal canal due to a skull which is too small
tethered cord — where spinal cord is “stuck” to a structure within the spine such as scar tissue
craniocervical instability — instability of head & neck bones compressing the brain stem or upper spinal cord.
Other spinal conditions that could cause or contribute to ME/CFS/FM/POTS include cerebral spinal fluid leaks and intracranial hypertension.
Even if you don’t have CCI/AAI, the search for it may help uncover other problems. One person on the Phoenix Rising forums reported that she didn’t have CCI but that the search for it turned up “severe stenosis, edema, compression fractures, and other issues causing my spinal cord to be affected” and that treatments for those conditions were helping."
"For me, the recovery stories provide hope and are a sign not to give up, to stay curious, to keep reading and asking questions. Medicine, as Jen Brea noted in her recent blog, is ever-evolving. What was cloudy yesterday may become clear today. It wasn’t that long ago that CCI/AAI surgery wasn’t even considered for Ehlers Danlos Syndrome – it was the province solely of whiplash and trauma patients.
We should also remember how vitally important sharing our stories – both our ME/CFS stories and our recovery stories is. Jeff’s publication of his story may have saved Jen’s life. It’s now enabled 20 people to be diagnosed with CCI/AAI and three are undergoing surgeries. Please share your improvement or recovery story.
Our goal has to be to assist the medical system in its evolution, to keep the hope alive, to keep sharing, to have the courage to keep knocking on closed doors, and eventually getting the light to shine through."
Read the full article if you've got the spoons
#cci#me/cfs#chronic fatigue#myalgic encephalomyelitis#eds#jennifer brea#unrest#chronic fatigue syndrome#undiagnosed
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Or even tips for someone who sits/lays down all the time. (Fellow bedridden folk?)
I can't sit up without getting a migraine, or worsening neck pain, and my shoulders keep being pushed forward and it's inflaming my costochondritis. My entire ribcage feels like it's being crushhed into a ball. Sudden sharp stabs of pain under my collar bone from the odd shoulder positions.
When I make art, I'm somehow I'm sitting in a position that causes more fatigue and pain.
So now making art has more of an impact than a day filled with super duper light physical activities.
Move around more is a good tip.
"Get that spine checked out" is something I'm working on.
But the chair situation.
I have no idea what to do.
I felt like gaming chairs might be a good way to go. Possibly...
And then there's the truth that you never really know what you're getting until you're sitting in it. And I can't get out to try any.
And a trusted ergonomic chair is an expensive investment.
I sit 99% of the time. 1% is just me walking to the bathroom or kitchen.
Heating pads, OTC pain meds, stretching and massaging neck muscles are not helping.
(Bah, I guess what I need it a guide on being bedridden lol?).
I know this is kinda vague.
Does anyone have experience with this type of thing?
Does anyone have recommendations for ergonomic seating with connective tissue disorders?
#eds#connective tissue disorder#marfans#ergonomic chair#spoonie asks#pain question#chronically ill#bedridden#disabled artist
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Sincerely,
Thank you.
#webcomic#art#drawings of You#comic#spoonieartist#spoonieart#need image descriptions#need description#Slowly Made Comic#forest art#glow art#digital art#space art
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Does anyone have recommendations for ergonomic seating with connective tissue disorders?
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Please check out this kevin Temmer animation "The common cold discusses their rival". 😄☺️
I hope you're all at least mostly okay. I hope life is treating you all with kindness during this chaos. Keep safe 💙🌿
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Wakey wakey, occult for your achies (achys???.......achies.... ...)
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Character art for supporter and fellow Rachel-name-haver, @traveltigress ^o^ 💚
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Hi all,
I’m looking for people who have Ehlers-Danlos Syndrome to take part in a study. I have EDS myself and I have decided that I want to do psychology research into it for my psychology undergraduate dissertation.
The study is looking at how beliefs of stigmatisation by others, self-stigmatisation and perceived control impact life satisfaction in those with EDS. This is an area which hasnt been explored in EDS research before and so the research will be the first of it’s kind! Also the study is completely anonymous so no one will know who has taken part.
Please let me know if you are interested or not or if you have any questions at all let me know!
Please dont feel like you have to take part, but it would be great if you could, or even if you could just share this post!
All the best!
This is the link for anyone who wants to do the study -
https://buckingham.onlinesurveys.ac.uk/to-what-extent-do-perceptions-of-stigmatisation-by-others
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