chronic illnesses
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xmagnet-o: dixie-wolf: Sometimes I’m like, “I have a chronic illness and that’s fine! I’m going to take it easy, because that’s what my body needs!” Other times I’m like, “Fuck this shit, I’m gonna carry 16 bags of groceries at once,
The Extra Burdens Faced by Young People with Chronic Illness
spondylitis: Living with a Chronic illness…..Be kind because you never know
worldaccordingtolupus: Life with chronic illness Find me on www.facebook.com/worldaccordingtolupus
Things I’m good at - Chronic Illness version:
that-fibro-life: Having a chronic illness is like playing life on expert mode. 3x the damage, ¼ of the energy, 20x slower recovery rate, and ineffective health potions!
spacejamonbluray: I feel like there’s a lot of emphasis with chronic illness on the people who are pushing through it, who suffer with smiles and that’s good and we deserve recognition when we can do that But here’s to those who don’t. Who can’t.
for-your-malice: The best part about having a chronic illness is getting to feel guilty about being sick all the time. Two thumbs up.
mrkittyboy: weegieinwales: ithotyouknew: veganthology: What is the justification behind eating meat and animal products other than “they taste good”? -having chronic illness and a fuck ton of allergies and food sensitivities which limits your
samstummyproblems: The thing that kills me about chronic illnesses is that you can do everything right and still be sick. You can be on the best medications, eat the best food, exercise seven days a week, sleep eight hours every night, and still be sick.
Trying to ignore my chronic illnesses like
memyselfandibd: The thing about living with a chronic illness is we go through all the same day to day life problems as the average human. We love, we fight, we grow, we loose. But the difference is on top of all that we are fighting are own internal
amplifiedpain: being chronically ill is really really hard. emotionally and physically. it’s hard to know you have a life full of appointments and tests and needles and procedures. it’s hard to know that each day might bring the same struggles as
fibro-larious: recoveringfromcfs: stanley-tsaii: Just a set of quick photos I did for class. Chronic illness 101. This is a simple yet beautiful depiction of thousands of people’s daily lives. Everyone who does not understand the Spoon Theory or
scienceblue: a-wooden-ring: So if you are disabled/chronically ill like me and depend on Obamacare for your insurance, now is a REALLY GOOD TIME to schedule that procedure you’ve been meaning to asking your doctor about. We have a solid four months
Just a little PSA for my other friends with Chronic Illnesses:
Never Get a Chronic Illness
dovesong:The amount of time, money, and sacrifices it takes to manage and live with chronic illnesses is overwhelming to say the least.
gwallamama: My life got so much better today, it’s amazing how things can just switch up on you so fast. Loving yourself with a chronic illness is very hard and I’m slowing getting back to the place I want to be.
starstarparty: IT’S OK IF YOU NEED MEDS EVERY DAY!Mental Health/ Chronic Illness positivity!I have this design available in Button and Sticker Forms too on my shop!!!
I have twisting knives in all my bones and muscles.
First I got the great news yesterday about my chronic illness. And now, not only might I have a Walgreens job, but they may eventually offer me a place in the pharmacy, which would mean they’d pay for me to take the tests and become certified. 2017,
My chronic illnesses have been flaring up very painfully lately, I can’t sleep anymore and the terrifying nightmares are back,and my joint pain has been so awful that i feel like I'm75 years old. It’s hard to be positive but I’m trying.
Well the good news is I got my thyroid meds refilled. No more being nauseous 24/7. Now I’m starving all day and night. I can’t sleep, and I can’t eat a full meal without feeling like I’m even hungrier than before. My stomach is
When your hypothyroid flares up and it’s only 77*F in the house
I’m in a lot of pain from my chronic illness and I’m driving 600 miles tomorrow morning with my dog and I’m already tired tomorrow.
It’s just so incredibly frustrating to be depressed again as a side effect of Hashimoto’s. Logically I know it’s my disease, not me,but it’s no consolation. I’m so tired of being tired.
doctorsebastianthescientist: kamorth: doctorsebastianthescientist: Hey, unpopular opinion, apparently. But people don’t just “have pain for no reason” doctors say this all the time (especially to women and chronically ill people) and the truth
fuckyeahfeminists: iwakeupblack: native-detroiter: raretowelldone: beatainspace: nuestrahermana: livingstrong4us: Any Questions? Hmm, I was under the impression that this blog was about chronic illness, education on it, spoonie community… not
antifasith: vortexsophia: “This is not a novel to be tossed aside lightly. It should be thrown with great force. ” Dorothy Parker Also elderly and chronically ill people don’t exist in this universe
tiredtrauma: Just because you’re young doesn’t mean you can’t have physical problems. Just because you’re young doesn’t mean you can’t be disabled. Just because you’re young doesn’t mean you can’t be chronically ill. It’s not your
whatsuprubberduck:My Mum didn’t raise no fool. Maybe a broken shell, with multiple chronic illnesses and questionable coping mechanisms. But no fool.
ri0t-grrrl: Shout out to all my chronically ill homies who are struggling as much as I am today. Special mention to those whose symptoms are worsened by anxiety, but who suffer anxiety as a result of their symptoms.
Things people newly diagnosed with chronic illnesses should know
I Won't Apologize for Having Fun While Chronically Ill
repotting: As a disabled fat person with multiple chronic illnesses and health issues, some of which are probably caused or influenced by my weight, I am so. fucking. tired of fat positive spaces essentially throwing me under the bus by saying “you
kinkyhippieprincess: housewifeswag: to those of you living with chronic illness or who just need to hear it, I know you may not feel well today but you’re strong and I’m so proud of you for everything you’ve accomplished today. however small or
crapchronicles:My idea for trying to remember to eat as a neurodivergent and chronically ill person:Also, for remembering meds…Thanks to @chungovscrungus for photoshopping these for me. You are a true artist.
weaver-z:weaver-z:Not to get serious about a meme, but Morbius should have been a comedy. The idea of vampirism being the only way to cure a chronic illness is extremely funny. Imagine being in a support group with this goth guy and one day he’s
glitterzits: chronicallyinvisible: i’m so sorry you all have to deal with everything that accompanies chronic illness…pain, medication, stigma, judgement, exhaustion, emotional distress, depression, ostracisation, isolation, misunderstanding, doctors
kamorth: doctorsebastianthescientist: Hey, unpopular opinion, apparently. But people don’t just “have pain for no reason” doctors say this all the time (especially to women and chronically ill people) and the truth is, Thats literally not possible.
prridot: fibro-larious: recoveringfromcfs: stanley-tsaii: Just a set of quick photos I did for class. Chronic illness 101. This is a simple yet beautiful depiction of thousands of people’s daily lives. Everyone who does not understand the Spoon
@ disabled + chronically ill trans people
0% okay with my chronic illness
That's the thing about chronic illness
thefaultinourstarscream: I’ve noticed that being chronically ill gets old for the people around you real quick at first they show concern and send you well meaning “hope you get better” messages etc. but when it lasts longer than a few months,
associatedrants: Hank Green made a video about how sometimes offering ‘advice’ to someone with a chronic illness is a shitty thing to do, and this comment is my new favourite thing.
looking for good books with disabled and/or chronically ill protagonists?
lymefight: my-mad-fat-fibro-diary: I don’t think abled people understand the amount of time and energy being chronically ill actually takes up. It’s like a constant battle against our bodies every single day. Truth. Full on battle everyday. No
lesbianartemiscrock: when you’re a teenager with a chronic illness– no standard any adult sets in your life is realistic to what you can accomplish and it’s exhausting constantly disappointing them
sadgaywerewolf: Ya’ll listen ok here’s the thing about being chronically ill: every remedy or cure or treatment that you’ve read about or heard about or seen, we have too. We know about it and we’ve probably tried it because you reach a certain
drowninginsideofmymind: I really wish there could be more chronic illness representation in TV and film. Subtle things. A two second shot of a teen taking enzymes with lunch at school sitting with their friends making fun plans for tomorrow. A two
heyatleastitsnotcancer: I hate when people say “overcome” a disability or chronic illness. You don’t overcome something you will have the rest of your life, you learn to live with it and adjust around it.
biomagnify:SUPPORT FEMME TRANSBOYSSUPPORT TRANSBOYS WHO DON’T WANT TO TRANSITIONSUPPORT TRANSBOYS WHO DON’T WANT TO CHANGE THEIR NAMESUPPORT CHRONICALLY ILL TRANSBOYS SUPPORY TRANSBOYS OF COLOUR SUPPORT CHUBBY TRANSBOYS SUPPORT ALL TRANSBOYS
whatsuprubberduck: My Mum didn’t raise no fool. Maybe a broken shell, with multiple chronic illnesses and questionable coping mechanisms. But no fool.
More so than usual.
radhg: spoonie noun; people that live with chronic illness; measuring their abilities much as one would measure the proper amount of spoons needed for an event or occasion… sometimes having an abundance, other times coming up short. in other words,