she/they/any pronouns|| 21 || lesbian || disabled || chronic pain and hypermobility || POTS and LongCovid || autistic and adhd ||

298 posts

Cw: Food And Discussions Of Eating

Cw: food and discussions of eating

Please let me know if I should add other CWs to this post

So every weekday I have a routine. I go to a specific dining hall on campus and I order the same 3 things every time (except when they don’t have it which causes other issues for me with the day just being wrong after that). Now I did this today but today is also a bad POTS day and it’s made me nauseous so I have a plate full of food in front of me and I just can’t get myself to eat it. Now I know I need to eat it and if I don’t eat it my day will feel off and what not. Idk what to do I also don’t want to waste the food.

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More Posts from Consider-your-potatoes-mashed

Thank you @autism_sketches

"STIMMING: What it feels like from the inside"

In the beautiful images that follow, Autistic artist & storyteller Anouk of @Autism_Sketches depicts the experiences of some of their Autistic followers on Instagram. It is so important to learn from Autistic voices. These descriptions are exquisite.

Thank You @autism_sketches
Thank You @autism_sketches
Thank You @autism_sketches
Thank You @autism_sketches
Thank You @autism_sketches
Thank You @autism_sketches
Thank You @autism_sketches
Thank You @autism_sketches
Thank You @autism_sketches

Universal Studios Hollywood was an amazing experience yesterday! And honestly was super disability friendly (from my perspective at least). Accommodations were easy to get and we’re not a hassle at all!! All the staff was super nice and always made sure I would be able to ride the rides/experiences. I’m so happy that it is the way it is. Also, having my crutches was LIFE CHANGING omg sure I was in pain yesterday, but it didn’t get to a point where I couldn’t handle it and today im not in a flare which is AMAZING!!!

Tl;dr: Universal studios Hollywood was an amazing experience and super accommodating and holy shit having my forearm crutches made my life so much easier.


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Me: “my pain and fatigue and everything else is getting worse and doctors still don’t know what to do about it”

My mom: “ well the problem will fix itself and you’ll get better and then it won’t matter”

Me (internally yelling in my head): THATS NOT HOW CHRONIC ILLNESS/PAIN FUCKING WORKS MOM I HAVE TO USE A CANE (AND NOW CRUTCHES) TO GET AROUND OTHERWISE ID BE STUCK INSIDE


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POTS really gives you a skewed understanding of heart rate. Like when I sat up this morning my heart rate was at like 180 and finally (30 min later) it’s calmed down to 135 and I just said to myself “eh well that’s not too bad” keep in mind I’m still sitting. Some people I know (who don’t have POTS) would have trouble handling heart rates in the 120s- 130s and that’s just wild to me

Let this also serve as a reminder to take care of yourself and don’t push it on flare days please


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