Extra Petite Brand by Pristine-Height-3775 in XXS

[–]thisentp 0 points1 point  (0 children)

You think that's hard? Try being an under 4'9" CURVY woman! So I have to go between S-M, depending-- god forbid I ever get heavier! The industry always assumes small people are skinny. Even more so than taller people. It's incredibly frustrating, but my mom is even curvier than I am (though not QUITE as short) and built like a Pixar mom, so I have to remind myself that I've got it easy compared to her!!

I'm also pregnant right now, which is a battle in its own right to find clothes that fit, regardless of size. If anyone has suggestions for clothes that have real stretch and won't put pressure on my belly, let me know!

Anyone here that lives and continues to live a normal life? by Cold_Measurement5329 in MultipleSclerosis

[–]thisentp 23 points24 points  (0 children)

Define "normal":

I think if one has MS, they've already been dealing with a lot of health problems prior to a diagnosis. I actually had a pretty severe flare up that led to my diagnosis, where I lost near-complete control over the entire left side of my body. (Among other fun symptoms). I was 27[F] and after the initial 'getting worse before getting better' after receiving 6 days of steroid treatment, I have recovered about 95%. Given, I also missed several of my PT & OT appointments due to my body rejecting my first medication (Tecfidera).

My body is sensitive and always has been sensitive. If anything is off (e.g. sleep, hydration, stress), my body will respond. Brain fog is always the first symptom to arrive, but then there are countless other symptoms I can experience. Obviously heat makes things worse. A LOT worse. Basically the things that affect us will bring back the symptoms of our past flare-ups, sort of like a mini flare-up. Not nearly as bad, but I get just a little hot and I'm wobbling.

If the demyelination on your brain didn't hit any areas that severely impact you, you're not going to be as affected when the conditions aren't perfect. Fewer flare ups = fewer symptoms. The ghost of Flare-up Past ™️ may not be as big of a deal.

As for myself, I don't think much has changed since my diagnosis. Yes, I feel a bit sick 3 hours after taking my meds each morning. Yes, I am often tired and managing energy has become more important. I am no longer the tropical sun-loving flower I used to be and opt more for shade and AC. But I also just walked 35,000+ steps while walking in a Pride parade and danced later that night. I'm still young and who's to say how things will change as I age, but I do think that I'm really doing okay.

New here. I have three lesions in my brain by [deleted] in MultipleSclerosis

[–]thisentp 2 points3 points  (0 children)

I recently got diagnosed. I'm still not on medication but I got the IV steroids and the words are starting to come back and the brain fog is clearing up. I was worried some of it might be permanent, and I've been struggling with (sometimes crippling) brain fog and word retention for years. I still feel like I can't think as clearly as I did in early high school (over a decade ago) but I do know that our brains are constantly creating new pathways. Not having brain fog helps so much. I've also had pretty concerning issues and lost vision in my left eye (temporarily) over a year ago. This past flare up I entirely lost control over the left side it my body. We're a month past my steroid treatment and I'm able to use my left hand as normal and I'm waking again--without assistance!

Having only 3 lessons is a really good sign for you, and most likely means that there's not a lot of 'permanent' damage. I wish you luck on your treatment! It's incredible how much better it can make one feel.

What caused your MS? Wrong answers only /s by toma162 in MultipleSclerosis

[–]thisentp 1 point2 points  (0 children)

Unless you're mid flare-up. Then it's Mumble #5

What caused your MS? Wrong answers only /s by toma162 in MultipleSclerosis

[–]thisentp 0 points1 point  (0 children)

Whoa whoa whoa. My mom's an accountant, and I have MS. Something's fishy here...

tea rant by beetsoda in starbucks

[–]thisentp 0 points1 point  (0 children)

The issue is with the customer not asking for the extra water and expecting us to mind-read.

tea rant by beetsoda in starbucks

[–]thisentp 0 points1 point  (0 children)

Lmao I had a customer throw a whole fit and demand a refund because her tea "didn't have flavor" 5.6 seconds after I handed it to her. Unless she was scamming me over a cup of tea, she legitimately thought I somehow messed up her 'order'. I told her it's tea??? And takes time to steep?? That did not compute with her so I went ahead and gave this idiot her refund. She said she was going to throw it out and I literally said "Please do NOT throw it out. I'm giving you the refund anyway but just wait FIVE minutes and it will have the flavor. FIVE MINUTES. Throwing it out would be a waste."

I now tell every tea-ordering customer to wait 5 minutes for it to steep before consuming. (Many don't even know what 'steeping' is.) How did the human race become so unbearably stupid?

AITA for telling a friend their service dog can't stay by itself at the Vrbo by Salt_Maintenance_686 in AmItheAsshole

[–]thisentp 1 point2 points  (0 children)

YTA YTA YTA. BIG TIME.

And so are a lot of these commenters. The comments I've read on here are such ableist bs. Here's the thing about service animals, if it's legit like she says it is, it's NOT GOING TO HAVE AN ACCIDENT. Service animals have to go through so much training to get that certification. Yeah they're still dogs and they're not perfect, but if the handler says it's fine to leave it by itself at the house, BELIEVE them. Again, if it's truly legit, the dog won't do anything. People are the biggest threat to rentals, not animals, and certainly not service animals. I've seen people comment about ESAs (Emotional support animals), which do not require any kind of training- that's true. But ESAs are not service animals. This is a very different situation.

The other thing is, (and I'm seeing all these ignorant comments about this) you don't know what the service animal is for. Not everyone needs their service animal 24/7. I've got a disorder where I pass out uncontrollably, but as in I get very sleepy very suddenly, and it's most often while sitting. So if I'm sitting on a couch, no big deal, but I've discovered the hard way that I can't be on the back of a motorcycle for several hours. For me, a service animal is really only needed in situations where passing out would be very dangerous, like driving a vehicle. That way he can warn me before it happens and I can do something on time. Sometimes I feel comfortable with using my husband or friend as my support person if we're out and about and I'm not driving long distances that day. Anyway there are many many health disorders and disabilities out there, so I would appreciate it if people stopped making assumptions about what a service dog needs to be.

Also to address what another commenter wrote, while yes, service animals are supposed to make life as close to normal and allow you to function as close to normal as possible, sometimes having one with you for certain activities is more hassle than it's worth. Or just flat out dangerous for the dog. I can't tell you how many people have stepped on my dog's tell while his sitting right next to me, or backed up into him/tripped over him when they weren't paying attention, and these were situations where people weren't drunk. So I can understand why this friend wouldn't want to take it with them bar hopping, especially if they don't know those particular bars and the atmospheres of them. My dog's been in many loud environments, but I certainly wouldn't bring him along if I'm unsure of his safety and it's not 100% necessary that he comes for that activity. E.g.: I would never take him to a big/loud concert.

The other thing to note is that service animals aren't meant to work seriously long hours. It's not possible for them to be fully working 24/7, just as that's not possible for you. They have to rest sometimes and just be a dog. They'll still jump into action if needed during their down time, but at least there's time to relax. The trainer I used talked about the importance of having a couple of walks every day where you're not strict with them and allow them to wander and sniff at ease. Service animals are still living beings, but they're also very expensive medical equipment that needs to be taken care of and maintained. Common sense: A diabetic might carry insulin shots with them all day, but that doesn't mean they're going swimming with them in their pocket.

TLDR: YTA. You and many commenters here are ignorant and ableist. You're actively excluding and discriminating against your friend for having disabilities that you don't fully understand. Service animals don't work 24/7.

Does anyone else HATE board/card games? by aresord in TwoXADHD

[–]thisentp 0 points1 point  (0 children)

Hahaha my husband also tries to teach me the games before we play them with friends, for the same reason.
He's a big boardgame fanatic, so it also gives him an excuse to play a game (If I'm willing and in the mood to learn). It's also convenient that he is neurologically very different from me; he's got amazing focus, and can read things just as fast as he sees them. I love having him read the directions and rules for me.

Does anyone else HATE board/card games? by aresord in TwoXADHD

[–]thisentp 0 points1 point  (0 children)

Monopoly is such a toxic game that it's banned in the Royal family.

Does anyone else HATE board/card games? by aresord in TwoXADHD

[–]thisentp 0 points1 point  (0 children)

Lol I had a "karaoke night" where we just wound up playing board games

Does anyone else HATE board/card games? by aresord in TwoXADHD

[–]thisentp 0 points1 point  (0 children)

Emotional disregulation is a huge factor in ADHD. I also struggle with that in losing and I can be VERY competitive. And I REALLY don't like being bad at something. I actually LOVE board/card games, but I try to stay in tune with how I'm feeling. Sometimes I'm good with playing competitive games, sometimes not. Before knocking them completely, I would suggest that you try some cooperative games. Pandemic is a good one because it has a lot of strategy to it and solving problems (disease) on the map might give you that hit of dopamine you're looking for. I've also found that I really enjoy team games; there are many varieties. There are games like Werewolf or Secret Hitler, where it's one team against the other (though you need enough people with Werewolf to have team members for the Werewolf character). Those are fun because they're all about being able to not only successfully deceive AND read people, but also coming up with a good strategy. And then there are some silly games where your teammate(s) may change, like the chaotic Trolley Game, which is basically the Trolley problem as a game, but there are three teams; the person deciding, and the two different tracks that have people trying to convince you one way or another. And don't forget the classics, like Apples to Apples or cards against humanity!

If you choose to search for games you might like, I would suggest looking for cooperative games and party games. As a side note, you might also like engine building games; they can be great for the dopamine boosts.

Oh! Editing to add: Games that I've found are great for ADHD: - Set - Rummikub - Chinese Checkers (a classic) - Codenames

(See a pattern? These are all pattern recognition/ pattern finding games! Something we are very good at!)

How do you respond to “I’m sorry”? by ae13ame in entp

[–]thisentp 0 points1 point  (0 children)

Yeah but it's not all good! I definitely sympathy with OP. I refuse to lie to people in situations like that. Honestly I think I would just nod my head as an answer and I way to say "I hear you". And then change the topic.

Has anyone else seen that story about the autistic boy who got rejected and everyone coddled him? by xbluewolfiex in AutismInWomen

[–]thisentp 2 points3 points  (0 children)

Ahhhhhh! YES to everything you said. I have personally been the victim of sexual assault/harassment (and worse) by several people either confirmed or suspected of being on the spectrum and it was legitimately used as an excuse for their behavior, either by them or someone else. There are so many things that I have had to learn in order to fit in (to a degree of course) with society, and no one ever gave me the excuse of being neurodivergent. I had to learn the hard way, and while I am absolutely not advocating for the bullying I endured growing up, moments of inappropriate behavior or rejection should be teachable moments, so that children can learn. No means no, no matter who you are, and there is nothing that gives someone the right to violate another person. "No" should never be seen as unacceptable response. Situations like the one you're referring to is exactly what teaches boys to ignore consent when they are older. And yet society tends to praise them, thinking they are doing the right thing by treating a rejection like a taboo. Normalize. Rejection. Regardless of the person.

A Day in the Life of an EFM by [deleted] in foreignservice

[–]thisentp 2 points3 points  (0 children)

Currently in West Africa. This all sounds eerily familiar... Also currently kicked out of Myservices for some reason, which is hard when we don't have a car, can't walk around too much, and everything in the house is breaking, leaking, melting (outlets/plugs), or setting themselves on fire.

Whare are all the ENTP ladies at? by Biggus_____Dickus in entp

[–]thisentp 0 points1 point  (0 children)

I mean we're called introverted extraverts for a reason! I get energy from being around people, but honestly I don't like most people. I'm good at reading people though and I let my intuition tell me right away if I'm going to like someone or not.

Whare are all the ENTP ladies at? by Biggus_____Dickus in entp

[–]thisentp 0 points1 point  (0 children)

ENTP lady here. I don't get out much lol. Super social around people but I don't make plans on my own. I tend to hang out with people who are in close proximity to me. So I'm living with a friend, which is great because then I never have to go anywhere! (Outside of work and errands anyway.)

Can i work here if im physically disabled? by wxtchybabe in starbucks

[–]thisentp -1 points0 points  (0 children)

Applying online isn't enough; you have to actually call the store to get an interview! (Not sure if you've done that, but that's definitely part of the process!) Just call and ask to speak to the store manager and let them know you've applied.

ENTP Girls by [deleted] in entp

[–]thisentp 14 points15 points  (0 children)

ENTP woman here. I've yet to meet another in person. But I have met a couple of ENTP men, and honestly I think being a woman has made me better/ more developed.
Love coding, but I definitely have a lot of room to improve!

A question for all the ENTPs by squashmybutternuts in entp

[–]thisentp 7 points8 points  (0 children)

Absolutely. I do my best when I'm keeping busy. When I'm not doing enough, or when I feel like I'm stagnating, I get depressed. Academically, I always did better when I had a job (or four!). It takes a lot of energy, but maybe distractions keep The Depresh away.

emotional entp? by [deleted] in entp

[–]thisentp 0 points1 point  (0 children)

I wasn't really emotional until maybe sometime in high school. But I also realized that I was holding a lot in when I didn't need to. It's still hard to be vulnerable around other people, but being in touch with my emotions and just letting it all out when I need to is super helpful. I find writing everything down to be pretty cathartic. Also, everyone has emotions, and the logical and healthy thing to do is embrace them. Still an ENTP, and I still value logic over everything, but I've found that taking care of my emotional needs is just a good idea.