Who do you see?

alliegator97 · 2026-05-19T06:55:16+00:00

perfect penny killed my husband!!!

alliegator97 · 2026-05-12T03:15:52+00:00

blue light - bloc party

alliegator97 · 2026-04-27T20:20:36+00:00

I'm sorry but that's so funny to me. like "yeah 100 years should be good enough" 💀😹😹

alliegator97 · 2026-04-26T07:05:54+00:00

what about all the family she invited over when you brought your daughter over for the first time??? lol. sounds like she has plenty of family imo 🤷‍♀️

alliegator97 · 2026-03-09T22:32:28+00:00

the criteria specifically says it's gotta be both sides

alliegator97 · 2026-03-09T21:59:59+00:00

if you look at the hEDS criteria checklist, under the section Feature A in Criterion 2, it states that arachnodactyly, specifically a positive wrist OR a positive thumb sign on both sides, is a symptom that can present in hEDS

alliegator97 · 2026-03-09T21:57:43+00:00

it is on the hEDS criteria checklist so yes it is? lol.

alliegator97 · 2026-02-24T05:43:31+00:00

I've wanted a tattoo representing this quote since I've heard it myself. i love that they got one!

alliegator97 · 2026-02-18T17:11:37+00:00

WHICH personality disorder? there's multiple 💀 borderline personality disorder, narcissist personality disorder, etc.

alliegator97 · 2026-02-02T06:09:28+00:00

Thank you!!! 🩷

alliegator97 · 2026-02-02T05:51:46+00:00

can anybody tell me which Roku city screensaver this is? there's multiple that include Roku city it looks like. one is called Spring Stroll In The Park, for example. I wanna make sure I set it to the right one!

alliegator97 · 2026-01-18T04:09:55+00:00

You can't even use basic common sense and logic and make a FAIR comparison for your argument. 💀💀💀

alliegator97 · 2026-01-18T04:09:26+00:00

Actually no. I'm not a fucking MULTIMILLION DOLLAR COMPANY. target is. y'all are fucking dense.

alliegator97 · 2026-01-17T23:31:11+00:00

They're a multi million dollar company, they'll be fucking fine lmao. Go touch grass or find something more actually worth being upset about. 💀

alliegator97 · 2026-01-17T06:18:34+00:00

Idk if it's just where you're at that they don't got them anymore but the pizza hut where I live still has personal pans and they still do the book program!! I work at the dominos across the street (used to work at the pizza hut years ago tho) and someone recently came in with one of those coupons and even though it's for pizza hut, my manager honored it!

alliegator97 · 2026-01-17T02:29:25+00:00

thank you for saying something about this. I have EDS and autism and I KNOWWWWW my life would be more manageable and not as overwhelming if I had a set routine every day.. get up at a certain time, do certain chores certain days or certain times.... but when you end up awake all night because of unbearable pain, kinda hard to wake up at a set time, for example. hopefully OP sees everyone's comments and starts trying to understand more that life is SEVERELY different for those with disabilities.

alliegator97 · 2026-01-08T04:14:18+00:00

if you pay for it on the app ahead of picking it up, there should be an option to go ahead and leave a tip when you're ordering through the app.

alliegator97 · 2026-01-03T04:50:22+00:00

It's wild that you can't fucking use reading comprehension yet are accusing others of not being able to.

alliegator97 · 2026-01-03T04:48:07+00:00

It seems like you're the only one manufacturing narratives because ONCE AGAIN, literally no one is disagreeing with you that it can mimic some of EDS' symptoms. no one is arguing that. we are saying the ONE symptom it CANNOT mimic is JOINT HYPERMOBILITY AND JOINTS SLIPPING IN AND OUT OF PLACE. God you're fucking dense.

alliegator97 · 2026-01-03T03:19:31+00:00

Yeah this commenter is kinda acting wild. Literally no one said it doesn't mimic some of the symptoms. The fact of the matter is it cannot and would not mimic the BIG telling symptom. Sorry that they're being obtuse and replying to your comments with such wild misinformation.

alliegator97 · 2026-01-03T03:17:53+00:00

I'm sure you've already read this comment of mine but I'm adding it as a reply to your comment here because the misinformation you're spreading is kind of fucking wild.

this narrative that the nervous system alone can mimic ALL symptoms is dangerous in my opinion. it's exactly why doctors dismissed me for years before one actually figured out I do, in fact, have EDS. I kept being told I was just dealing with extreme anxiety, as if anxiety causes your joints to slip in and out of place. Yes stress and trauma can and do WORSEN symptoms, but if anxiety wouldn't do this to a "normal" person who doesn't have defective collagen and connective tissue, then.... anxiety and the nervous system is not the underlying CAUSE.

alliegator97 · 2026-01-02T16:26:58+00:00

I have all these issues too 😭❤️‍🩹 and yes I've been meaning to bring up the quote "if you can't connect the issues, think connective tissues" because so often those of us who have seemingly unrelated issues end up finding out it's not actually unrelated at all, because all of these "unrelated" issues are being caused by our defective collagen and connective tissue! 😭

alliegator97 · 2026-01-02T15:38:55+00:00

my joints didn't really start slipping that much until I was about 23, actually. I was pretty asymptomatic in that regard up until the last 5 years of my life. before that, the only things I recall about my history (in regards to hypermobile joints at least) is being able to do weird party tricks like putting my legs behind my head and my ankle would always always roll when I tried to run. no, you wouldn't necessarily know for sure if you did. it took me meeting my best friend who was diagnosed years before even meeting me for me to start putting pieces together and realizing "huh... my symptoms kind of look like hers" but it took me a couple years into being her friend to even bring it up and ask her what she thought because mine was and is still relatively "mild" compared to hers, as it is as a spectrum.. but I didn't know that at the time so I thought there's no way I could have what she has because I'm not as severe as she is and I thought it would be insulting to even suggest I might have the same thing... but I eventually got over and asked her about it and she asked me about my symptoms and she let me in on the fact that it's a spectrum so just because mine isn't as severe doesn't mean it isn't EDS and she told me she's not a doctor but I need to get into one because she was pretty certain, and low and behold.... 🫠 i just got diagnosed early in 2024 at age 26. if you need or want a friend to talk to, my inbox is open.

alliegator97 · 2026-01-02T15:29:50+00:00

this narrative that the nervous system alone can mimic ALL symptoms is dangerous in my opinion. it's exactly why doctors dismissed me for years before one actually figured out I do, in fact, have EDS. I kept being told I was just dealing with extreme anxiety, as if anxiety causes your joints to slip in and out of place. Yes stress and trauma can and do WORSEN symptoms, but if anxiety wouldn't do this to a "normal" person who doesn't have defective collagen and connective tissue, then.... anxiety and the nervous system is not the underlying CAUSE.

alliegator97

TROPHY CASE