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This body is a cage. When my symptoms force me to stay in bed, it’s not something I enjoy. It’s not something I want. I want to go to work, to class, to dinner, to parties, to the life I built for m
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The story of my spinal fusion hardware failure AKA how I ✨broke my back✨ in highschool 😀🫶🔩 I’ll have to make this multiple parts due to my reel time limit :’)) This video is from 2023 lol Commen
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Realizing I’ve never posted a full consecutive timeline of my long history of chronic illness that started at age 0 and is still going on today ✨ I want to make a YT video or podcast or smth going int
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this couldn’t wait one more week? 😐 do student loans next smh #college #gradschool #canvas
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Happy EDS Awareness month! ❤️🦓🧡 I was diagnosed with Hypermobile Ehlers-Danlos Syndrome (hEDS) 12 years ago at the age of 14. While I was extremely lucky and privileged to have access to knowledge
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This is why I don’t use binder clips 💀 + there’s many other ways to hold it but my hypermobile fingers just make it generally difficult 🤪 #hypermobility
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Disabled people belong, end of sentence. ♿️🤍 #DisabilityVisibility
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A small piece of what I’ve been working on at Harvard! Let me info dump real quick 🤓🦓 Patients are mislabeled, gaslit, dismissed, and have to battle the medical system while already fighting life-a
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a disabled scientist walks into Harvard with a ring light 🙂‍↕️ Boston !!📍🧃🚃🪲❣️ you’ve been so lovely to me these past few weeks :-) I’m proud of the work I’m doing in the @mediaandmed program
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no no no YOUR body is a temple, MY body is an Applebees 🤨 flare ups sometime make me disappear for days/weeks at a time, I don’t have the capacity to take care of anything but essentials and managin
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Hypermobile EDS neck ✨ What do you meeeaaannnn I’m not supposed to sleep with my ear touching my shoulder??? What do you meaaaannnn that has long term health consequences?? Get a lil scarf or t-shir
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hEDS is *NOT* rare ‼️ let’s get into it… ✍🏻 an excerpt from a research paper I’m working on rn: → EDS has been historically considered extremely rare; there were fewer than 100 documented cases by
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About @thesickshow_

Alyssa ♡ is a Instagram micro influencer. With 38.1K followers and 12 posts, thesickshow_'s account shows a follower-to-following ratio of 74.6:1. This profile demonstrates strong community engagement within its niche. View all content anonymously on Pictame - no login required.

thesickshow_'s engagement rate sits at 16.97%. That's 579% above what you'd typically see for accounts with 10K-100K followers (average 2.5%) — a sign of a genuinely connected audience.

Out of the last 12 posts, 92% are videos and 8% are photos. Notably, videos tend to get 414.8x more engagement than photos. Content shows up about every 57 days. Captions lean detailed, averaging 660 characters.

16.97% engagement rate — 579% above average for 10K-100K follower accounts.
92% videos, 8% photos. Videos get 414.8x more engagement here.
Posts about every 57 days.
74.6:1 follower-to-following ratio.

FAQs About @thesickshow_

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thesickshow_
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@thesickshow_

Alyssa ♡

Public
Posts
12
Followers
38.1K
Top Hashtags
#chronicillness#invisibleillness#disability#ehlersdanlos#scoliosis#spinalfusion#ehlersdanlossyndrome#eds

Explore the most impactful hashtags used in recent posts. These tags highlight the core interests and trending topics that define this profile's digital influence and content strategy.

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Popular Hashtags

#food#followme#photo#music#viralreels#life#ootd#motivation#friends#fun#like4like#me
Following
511
Avg. Likes
6.4K
Avg. Comments
113
Engagement
16.97%

chronically ill & loud about it ˗ˏˋ 🦓🫀🩻 ˎˊ˗ patient / scientist / artist 💌 welcometothesickshow@gmail.com

linktr.ee/thesickshow
#makeup
#selfie
#foryou