#spinals

[arunneronthird]

they get along great

[ultrakillblast]

THIS IS SPINAL TAP (1984)

[painedandconfusedsblog]

I don’t know who needs to hear it but it is not a moral failing if you are doing all that you can to relieve pain yet are not making a dent. It’s not your fault. Your pain is not your fault. Relief isn’t happening because your pain is mighty and under treated. Not because you aren’t trying hard enough. Your pain is not your fault.

[gayaest]

[OC] Saad 🍰🍨🍫 (description in alt-text)

[beebfreeb]

If I saw a nutcracker nobody could stop me

[crippled-peeper]

I hate to make another post like this but it’s the 1st day of disability pride month and I could really use a bit of help so I can afford my meds, food, and electric and phone bill 🖤 heres some pictures that explain part of what is wrong with me:

I am also bipolar I and take lots of antipsychotics to function. absolutely no pressure to donate if you are struggling too, here are my URLs:

I have PayPal too but it has my birth name on it so I would prefer to DM it to people 🖤✨ thank you all so much

[plague-parade]

happy disability pride to all of my fucked up spine havers

happy disability pride to those of us who have spinal cord injuries, degenerative disc disease, ankylosing spondylitis, scoliosis, kyphosis, lordosis, spinal arthritis, cauda equina syndrome, tethered cord syndrome, spinal fusions, stenosis, myelopathy, radiculopathy, spondylolithesis, craniocervical instability, spina bifida, spinal tumors, syringomyelia, and anything else spine related

we are so very cool and i love you all so much

[doubledaybooks]

These are the vibes I THE WHYTE PYTHON WORLD TOUR brings to the function bookshelf.

It's Spinal Tap meets Austin Powers.

It's an 80s themed wrestling duo alarming the interviewer.

It's Lorelei Gilmore Reading THE DIRT.

It's Ozzy Osbourne on reality TV.

It's "The Wind of Change" being used as a political battle cry.

Get ready for the world tour...

[archiepelago]

alternate surface au inspired by a few ive seen around on tumblr :3

[walking-loather]

I've always been curious to know this about the people around me. Most people have been in severe pain, but in my experience few have had what they would say is their 10/10 experience. I guess it's just something I find fascinating, as I had my 10/10 experience quite young and I sometimes forget that not everyone has. In my opinion it changes your relationship with pain and how you engage with it afterwards. If you answered yes, feel free to elaborate on your circumstances in the tags!

(reblog for a bigger sample size etc)

[winter-seance]

This Is Spinal Tap (1984)

[scramratz]

Hi mister scramratz

My name is Alejandro and im a 14 year old bisexual transman. Ive been watching your videos on tiktok foorr about a year now? Or atleast several months. I really love and relate to your content alot. I love hearing about your anecdotes and just your experience with this whole trans thing. You make me feel like im not alone and that there is hope even if life is dookie bum fart. I currently live in a VERY red and unaccepting neighborhood and am constantly teased for being an "emo lesbian" if i see someone who used to know me in middle school, god forbid. But i watch your videos alot after school and keep watching because of the relatability, honesty and humor you throw in the mix. Im an artist too and i hope soon, or when i get the experience, i can make comics/videos like you. You rock my guy. Dont let up!

From Ale

Thanks for this, Alejandro! I'll admit I teared up a bit. It's nice hearing how much my art means to others! I've been In a bit of a rut artistically this last month. To know that you and others not only like what i make but keep going back to it, puts my mind at ease. I wish I could post more often, but alas, I must work.

I'm sorry you live in an unaccepting environment. It's hard enough as an adult, I can't imagine how hard it must be as a trans kid. The fact that you are so sure of yourself so young leaves no doubt in my mind that you'll survive, though. If no one else believes in you, at the very least, believe in yourself. It makes life much more bearable. The good thing is, you're not alone! The world is filled with good people around every corner. People who will accept you without debate. People who will love you unconditionally. But you have to find them, and you have to let them know you, and that's the scary part.

Don't wait to make those comics. Do it now! Even if the anatomy is off and the lineart is shitty. The world needs more art, especially from folks like you! The scramratz comics started as doodles from the psych ward.

Just start, man. Start now and you'll be a pro before you're my age.

[trek-tracks]

one of the episodes of all time

[gleditsia-triacanthos]

paraplegia is not “disability lite”????

this is based on a recent in-person interaction through a support group.

i was paralyzed, in the grand scheme of things, SUPER recently, so i understand how it feels to be disabled in both an apparent way and a non-apparent way. i’ve had the condition that contributed to my paralysis (cEDS) my whole life, and it causes plenty of other complications.

it’s frustrating to have a non-apparent disability. there are unique challenges that come with having a non-apparent disability. it is ALSO frustrating to have an apparent disability. my treatment by other people has 100% changed since my sci, and not necessarily for the better.

a few ambulatory people seem to have this idea that being paralyzed from the waist down means you’re able-bodied sans your legs and you suddenly have endless empathy and help from society. this, i would hope goes without saying, is absolutely not true.

paraplegia is often caused by some underlying condition, meaning plenty of paralyzed people are also independently chronically ill. even in the case of injury or accident-induced paralysis, the paralysis itself causes all kinds of lovely symptoms, including muscle spasms and bladder retention or incontinence. i have to self-catheterize. incomplete SCIs can cause nerve pain. the act of using a manual chair to get around in public at all times can mean damage to the upper body and pressure sores.

i’ve had a few more doors held for me now that i’ve started going out in public alone, but being so apparently disabled also means stares. everywhere. not just from kids. it means people feel like they can push you out of the way to reach something in the grocery store. it means people will speak to you like you’re an elementary schooler. it means that even on your good days, other people will remind you of your disability and ask invasive questions about your “car accident.”

i’m not interested in the apparent-vs.-non-apparently suffering olympics, i’m just hoping to offer what seems like an underexpressed perspective.

peace + love. sorry for the rant.

[crippled-peeper]

how ablebodied people look at me after telling me they’d violently kill themselves if they had my disability