Gillian Flynn, Sharp Objects
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@chronicallyfuckedsyndrome
Gillian Flynn, Sharp Objects
We're not lazy. We're sick and it sucks.
We're not flaky or making excuses. We would love to join in.
We're not faking. We often wish we were.
We're not too young. Chronic illness and disability can affect anyone.
We're not being "negative". We're telling it like it is.
We don't "just need to try harder." We've tried that.
We don't want your supplement or diet recommendations. We've tried those too.
We don't want your pity. We would like your support.
Can I scream about DWP because wtfdym my claim has been ended based on me not providing requested further information in the correct time frame???!!!!!
I spoke to a call handler who confirmed an extension on both forms for the 11th July.
I asked at the time for it in writing as I struggle processing and remembering verbal information and was told oh no we don't do that so just wrote it in my call notes instead.
Also, I sent form 1 weeks ago (they didn't provide any acknowledgement) and I just needed to add a couple of attachments to form 2 before submitting đđđđđđđđ
And immediately proceeded to catch piping hot liquid on my lip which stings like fuck and is already swelling up. This day is going so badly.
Can I scream about DWP because wtfdym my claim has been ended based on me not providing requested further information in the correct time frame???!!!!!
I spoke to a call handler who confirmed an extension on both forms for the 11th July.
I asked at the time for it in writing as I struggle processing and remembering verbal information and was told oh no we don't do that so just wrote it in my call notes instead.
Also, I sent form 1 weeks ago (they didn't provide any acknowledgement) and I just needed to add a couple of attachments to form 2 before submitting đđđđđđđđ
The cyclical hell of waiting for symptoms to subside only for new ones to arise
Happy disability pride month to severely disabled people who are housebound/bedbound
happy disability pride month to severely disabled people who donât have access to proper treatment or medical equipment, and are stuck without care that would ease symptoms or make their life easier
happy disability pride month to severely disabled people who wonât be getting better, and who will be getting worse, or who will be dying due to their conditions
happy disability pride month to severely disabled people with photosensitivity who canât look at screens for long, and feel even more isolated by not being able to interact with much the disability community, even online
happy disability pride month to severely disabled people who arenât happy to be severely disabled, but are happy to be alive
Me: I'm doing so well lately, I'm sure I can do more stuff.
Also me, one day later: ... Now I remember why I did pacing...
Just a reminder, but you do not need to âearnâ being tired.
Youâre allowed to be tired, even if you havenât âdoneâ anything and youâre allowed to be tired even if you did less than someone else.
Being tired is a normal thing your body does for a whole plethora of reasons, and is a basic bodily function. You donât need to âearnâ basic bodily functions, no matter what anyone else tells you.
As someone who deals with crushing fatigue pretty frequently due to a chronic illness, I love this and would like to add:
It is NEVER a waste of a day to rest. Never, ever. My therapist and I have talked about this and they always remind me that resting when needed is actually an investment of time, not a waste.
Take care out there - and combat the mind-fuck around rest and tiredness as much as you can!!!
youâve been moving around a lot? FATIGUE!
youâve not been moving around? FATIGUE!
youâve been standing? FATIGUE!
youâve been sitting? FATIGUE!
you are simply conscious? FATIGUE!
youâre sad? FATIGUE!
youâre apathetic? FATIGUE!
youâre happy? HeadacheâŚAND THEN FATIGUE!
fighting ableism isnât about refuting the idea that weâre disabled at all
âautistic people arenât incapable!! look at me, iâm autistic and i can function exactly like an abled person!! everyone should be like meâ isnât anti ableist. youâre taking the stereotype from one end of the spectrum and moving it to the other and that helps no one
the answer to âdisabled people who canât contribute to society are worthlessâ isnât âall disabled people can do things if they try hard enoughâ. itâs âeveryone inherently has worth just by being aliveâ
Chronic pain sometimes manifests in wishing to be cracked like a glowstick.
so many people ive known have pushed themselves to burnout trying to deny their disabled reality, skipping accommodations, skipping rests etc. and the world convinces them that the solution to their burnout is to push even harder. itâs a huge tragedy. i know social pressures make it tough but i want more disabled people to make things easier for themselves where possible, to opt out of things that harm them when possible, to quit while theyâre ahead. be that person today! protect yourself where you can! take micro breaks while doing your hobby. get that shower chair. sit to brush your teeth. lie down in the middle of the day, even if only for 5 mins. these things add up and itâs so worth it.
One of the best things I've done for myself as a disabled person is get rid of my shame around sitting or laying in weird places. Bathroom floor? Check. Random sidewalk? Check. Lobbies of various professional buildings? So many checks. It is not embarrassing or shameful for me to take care of my body but it is embarrassing for architects and city designers to value appearances over accessibility
[the most low energy you have ever seen me] weâre about to go crazy mode
new free minizine: "Meditation 101"
just a quick lil zine to teach the basics of the style of meditation I landed on after 20 years of meditating. based in the Buddhist tradition but applicable to plenty of others - take the best, leave the rest. *note: the mistake in the preview isn't in the downloaded files; the program goofed when I saved the PNGs for some reason.
[[ available as a printable or read only copy - get yours here ]]
Wish I didn't *have* to spend so much of my life in bed