
we're a C-DID system, traumagenic, we post about whatever comes to mind. our collective name is moth or bug, we use he/they/it/xe pronouns collectively
154 posts
So Discord...
So Discord...
I'm curious. I know it's common for a lot of people to join servers and just lurk or join and immediately perma-mute BUT
edit: obligatory "reblog for reach" etc etc blah blah pls
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More Posts from Tons-of-moths-in-a-box
"cis men dni" are you ready to come out of your "no boys allowed" treehouse yet. its time for lunch.
Tips for all of my alternative & Chronically ill/ disabled friends!
A big thing that's helped me feel more comfortable accommodating my disability is finding accessibility tools that reflect my personality / interests.
I should put a disclaimer that making disability "aesthetic" should not be the most important thing about your health! I do this where I can to help me accept my disability.
Here are some alt accessibility tools I've found / made & utilized for myself!
1. If you're prone to nausea:
Anti-nausea meds work, but I also find that peppermints work just as well! I always have mints on me. At home, I've stored them in this coffin container!

I do keep a few of these mints in my bag, as well as ginger hard candies (they taste very strong, but are VERY efficient). I got the peppermints at Dollar tree, and they've genuinely been a life saver.
Alternatively, I've found this adorable ouija board altoids container that has mints in it!


The mints are even fun-shaped! I also saw other horror-movie themed altoid containers in-store as well. Since they're tiny, they dont work well for severe nausea, but they are still helpful!
2. If you struggle with temperature-regulation:
For me, my hands and feet are always FREEZING, but my core will be super warm. What has helped me a lot has been gloves and fuzzy socks!

I have a lot of spooky gloves like this, but I prefer the fingerless ones because I can still use my phone and be warm at the same time! I've also heard my friends who are wheelchair users say gloves can help protect your hands if you use a manual wheelchair. Another added bonus is that certain gloves can help limit mobility for those of you who struggle with hypermobility in your hands.
3. Do you have noise-canceling headphones? Decorate them!
I decorated my N/C headphones in shark stickers because sharks are my special interest!

These are Soundcore Life Q30's. I have gotten compliments on the stickers many times! You could put halloween stickers on yours or decorate your headphones in other ways! I've seen people crochet horns onto the headband portion of their headphones.
4. I would recommend any chronically ill person carry a cup around to stay hydrated:
ESPECIALLY If you need electrolytes. You can either have a drink like propel or powerade in your cup (or any drink of your choice, and you could put electrolyte packets in there).

This specific cup isn't the best at keeping my drink cold, but it holds a decent amount of liquid! And it's spooky. If you're someone who struggles to drink enough water, I've found that getting a fun cup helps me a lot!
5. Make communication bracelets!
If I'm having a difficult time voicing my needs, or I'm in a verbal shutdown, these bracelets can come in handy for me.

I'll either wear them on my wrist when needed or present them to my friends so they can read the bracelet and understand what I need. I keep them on a keychain that way I dont lose them and can transport them easily. An example of some of the phrases I've turned into bracelets is; "No spoons," "spoon debt," "verbal shutdown," and "flashbacks," (for when I'm having a PTSD episode.) You could make a bracelet with the medical condition you have as a DIY medical-alert bracelet. I added tiny spoon charms to some of my bracelets because I thought it was funny.
5. Mobility aids!
Decorate your mobility aids with things like stickers, kandi, lights, etc! Pinterest, instagram, and tiktok have a lot of good ideas. You can easily customize your mobility aids to look spooky or look however you want them to!
6. Bags!
I know that for me, I NEED to carry a bag around whenever I go out because it has important medical items that I need, but it also keeps all my important items like keys, id, ect, in one spot so that I dont forget / lose them. SOME spooky bags are expensive, but you could find a plain black bag at a thrift store or walmart and accessorize it with patches, keychains, and pins! I've seen people paint designs onto their bags before as well.
• You dont have to spend a lot of money on your accessibility tools!
Find ways to DIY them, or get them secondhand! You could even try working with household items you already have! A lot of these items, or items very similar to it, can be found at the dollar tree - even the materials needed to make the beaded bracelets! (Outside of the spoon charms)
Thats all!
If I think of more, you'll see me again! Be spooky, and be kind to yourself!
“women and enbies” “everyone but cis men” “afab people” “femmes and thems” “girls gays and theys” “women and everyone else” SHUT UP SHUT UP SHUT UP SHUT UP SHUT UP
Men, generally speaking, are not a systematically oppressed class the same way women are.
And that's not a go-ahead or justification to be racist, homophobic, transphobic, intersexist, ableist etc to men.
That's still bigotry and you're still a bigot. Bigotry isn't suddenly progressive if it's being directed at a man. That's not what hating the patriarchy means.
“Women nowadays are generally not punished for wearing masculine clothes or having short hair and are still seen as women while wearing/adopting those styles”
“All transmascs need to do to pass is wear masculine clothes and have short hair and people will recognize that he’s a man/masc”
Hm. These two statements I’ve seen in the discourse around transmasc oppression lately… how in the world are people not seeing how contradictory these things they’re saying are? Or do they just not care?