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#potsawareness
bluejayqueen · 2 days
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After matching with a guy on a dating app, we had chatted for a little bit as we got to know each other. I finally decided to just tell him my chronic illness. Not going to details, but just tell him that I have a chronic illness just to rip the Band-Aid off. To my surprise being asked questions about my illness, which was fine. however, he asked the question “does it affect you every day life?“. And at this point I was already scared because I knew that once I answered this things were going to change so I said, “yes it does affect my everyday life.” he immediately unmatched me.Obviously I’m disappointed because my fears came true. I am learning to accept myself, I wonder will anyone else accept me? There has been a little piece of me in the back of my mind who is scared that no man will want me. I don’t need a man. I will be fine without one. But with all this isolation, I can’t help but fantasize about the idea of having someone who loves all of me. I don’t wanna be alone forever.
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panicismydefaultstate · 7 months
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Just in case anyone else needed to hear this today-
Your health is not your fault. You didn’t do anything to “deserve” this. And you are right, it isn’t fair. You are allowed to feel upset, hurt, angry and jealous that your health, body or mind disables you.
It’s not fair, and that sucks. You are allowed to scream about that as much as you need to.
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justsomerandomgay · 2 months
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abled people don’t seem to understand why i try to avoid getting a cold like it’s the plague, like mate im literally chronically ill, i don’t need another illness on top of it!
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helios-hawk · 2 years
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i hate you breathlessness i hate you brain fog i hate you dizziness i hate you tremors i hate you joint pain i hate you fatigue i hate you racing heart
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valcksys · 1 year
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soooooo tired of people acting like my disability accommodations are a WANT and not a NEED
because it’s not a fucking want, I NEED these accommodations. Idc if they “inconvenience” you in some way. think about how inconvenienced I AM just by LIVING
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thecovenhouseco · 1 year
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Slowly realizing that you may not be able to work anymore if you actually want to treat some of your disabilities feels like you’re being crushed like a hydraulic press. I’ve worked so hard, and I’m afraid that it was for nothing. So if you’re struggling with the same thing, I’m proud of you for all that you’ve done.
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I’m so exhausted that I’m pre-exhausted for tomorrow.
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Its a staying horizontal type of day
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Happy rare disease awareness Day!!!
Reminder that rare diseases have less studies done on them, less available treatment and the diagnostic process can be a hellish 10 years journey of fighting with doctors to be heard,
and diagnosis can also be sudden and/or traumatic experience!!
All my love to people with rare diseases!
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fuck I hate having POTS all I’ve been doing for the last half hour is lay down. Why the fuck is my heart racing and pounding???????
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theriseofthesea · 1 year
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Me, literally just existing:
My heart rate 📈📈📈📈
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bluejayqueen · 12 days
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Is anyone else out here flaring up really bad because it's getting warmer out?
I'm out here fighting.
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helios-hawk · 8 months
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too nauseous to eat, even more nauseous bc I don’t eat 😭 I am like that fucking guy with the boulder
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curlyhairwitchgf · 3 months
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Like, even if you need to change your shirt or have a big bag
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faebobaggins · 3 days
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casual dating with chronic illness feels impossible sometimes. having to explain why i can’t go out to dinner, go hiking, or even get in a stupid hot tub. i can’t go to farmers markets on the weekends or go to concerts and genuinely enjoy myself without worrying about passing out. “nice to meet you! i like to lay horizontally and if i stand for too long i’ll faint. want to sleep together?”
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