Kase

joined 2 years ago
[–] Kase 2 points 6 months ago

Oof, that's harsh. I'm glad you managed to trudge through it. It's not unlike how difficult, if not impossible (and expensive) it is in some states (mine included :/) to get a legal name and/or gender marker changed.

They just gotta make it as hard as they can, don't they.. πŸ™ƒ

[–] Kase 1 points 6 months ago (1 children)

Do they? I guess they'd have to figure out why they're so set on getting that surgery, if it isn't a matter of skewed body image. Any treatment is going to have to depend on that, I'd imagine. Has there been research on this subject?

I sincerely doubt a doctor's first response would be to encourage the patient to get a BBL. Gender-affirming care (specifically here, hrt and surgery) has been extensively scrutinized and researched and has been proven effective for treating gender dysphoria, and other treatments (like conversion therapy) have proven ineffective. As far as I'm aware, the same isn't true of BBLs and (is there a name for this phenomenon?). From what you said, it sounds like BBLs aren't nearly as safe as gender-affirming care, so that might make it more difficult to justify. It's also worth mentioning that gender-affirming care is justified by just how bad the outcomes are without it (e.g. suicide rates, persistent mental health struggles, quality of life). Afaik, similarly negative outcomes haven't been observed in this case, but please correct me if I'm wrong.

*I'm typing this on my phone, but if you do want sources on the effectiveness and safety of gender-affirming care, effects of conversion therapy, etc., I'd be happy to provide them once I get home.

[–] Kase 2 points 6 months ago (3 children)

I just want to point out, gender dysphoria is different from body dysmorphia, though the words look very similar. A person with dysphoria (eg, a trans person) sees their body the way it really is, but is uncomfortable with it. A person with dysmorphia (eg, someone with an eating disorder) sees their body as different than it actually is, and is uncomfortable with that perception.

That said, you can't effectively treat someone experiencing body dysmorphia the same way you'd treat someone experiencing gender dysphoria, and vice versa.

[–] Kase 4 points 6 months ago (2 children)

Just to add, although the US allows informed consent for adults, some of us are still required to do a certain number of months in therapy and/or provide letters from mental health professionals before we can access hrt or surgery, because that's what some health insurance companies require. Even then, ofc, the option does exist to do informed consent and pay out of pocket.

[–] Kase 2 points 6 months ago (1 children)
[–] Kase 8 points 6 months ago

As a gay man- at least in my local community, the loophole does exist, and I've heard a good number of queer people use it (though only in conversations with people they know will be comfortable with it). 🀷

I don't necessarily take issue with it being used in a clinical tone like this. Context is context tho, and I don't speak for everybody ofc. °⁠_⁠o

[–] Kase 2 points 6 months ago

Ah well. Thanks!

[–] Kase 6 points 6 months ago (1 children)

I don't get it. What good reason is there for the state to make a law like this?

[–] Kase 5 points 6 months ago (2 children)

during the day, when there's plenty of light anyway

b- because of the sun, no? or is that the joke i'm missing lol

[–] Kase 4 points 6 months ago (1 children)

Ah fuck, I worded that poorly. No, talking about it is fine, but thanks for asking! I don't mean the physical sensation is the same, like how you can feel a bug on your arm. Speaking for myself, it's like the mental reaction of "ick there's a bug on my arm, I have to get it off". There's no physical itch or tickle on my skin. I was trying to make that comparison because generally when there's a bug on you, it doesn't bother you if you don't notice it, and you might not even realize it's there for a while. But once you notice it or someone points it out, it'd be hard to just ignore it, even if you couldn't feel it on your skin at all.

As I'm typing this out, I'm realizing that it's possible that not everyone experiences quite as strong a reaction to having a bug on their skin that I do, especially as a person with ocd, lmao. But if you do, well, hopefully this helps!

[–] Kase 9 points 6 months ago (4 children)

Not the person you responded to, but for me it comes and goes as a result of OCD. It does hurt, but not terribly. To describe the urge, it's a bit like if there's a big bug on your arm. Once you notice it, it's difficult to not immediately swat it away, and until you do get it off, you're gonna be very aware that there's a bug on your arm. It's pretty much the same feeling, just directed toward hair instead of bug.

It might be totally different for other people, but that's just my experience.

[–] Kase 13 points 6 months ago

mmmm *⁠.✧ tingles⁠ *⁠.⁠✧

 

Just curious. I looked through the settings and didn't see anything regarding push notifications, but I thought it couldn't hurt to ask in case I'm missing anything.

If not, are there any plans to introduce them? I wouldn't complain either way, honestly. I'm not sure if I'd even enable them. On one hand, they can be too attention-grabby. But without them, sometimes I feel like I have to keep opening the app to check. I know I'm a little phone dependent, but I'm working on it. ¯⁠\⁠_⁠(⁠ツ⁠)⁠_⁠/⁠¯

This is unrelated, but I just wanted to say thanks to the devs! I've been on here for a few months and it's been a great experience. Y'all rock :D

 

Hey Lemmy! πŸ‘‹

I've never been able to stand the feeling of wearing a wrist watch for very long. But I figured hey, maybe I just haven't found the right one yet! So I'm here to ask, what's the most comfortable watch to you guys?

8
Hello everybody :) (self.recovery)
submitted 1 year ago by Kase to c/recovery
 

Hi! I wanted to check in with the community (if that's okay), how is everybody doing? I wanted to open up a space for anybody to talk if they'd like to.

This week I passed the 2 month mark again, and I just wanted to share that with somebody, y'know?

I feel really proud of myself, but it's also a little hard to keep going now that it feels like I'm in for the long haul. My longest streak was almost 4 years, but it was very difficult. I want to set myself up better this time so it won't be as much of a struggle. (I'm working on getting back into therapy; I think I could really benefit from talking about it in therapy, not to mention making a new safety plan and everything.) I know I can't expect it to be easy, I just want to get to where I can feel more confident.

Recovery is heavy. I feel a little better just posting this, and I wanted to invite anybody else who needs it to share how they're doing here. I know we're just internet strangers, but I'm proud of you guys <3

4
Winter Weather Advice (self.wheelchairs)
submitted 1 year ago by Kase to c/wheelchairs
 

Hello! Manual wheelchair user here, and I'm wondering if anybody more experienced can share their strategies for going out in the colder months.

One thing I've yet to figure out is gloves. Do you guys wear gloves in the winter? I've yet to find anything that doesn't make it impossible to grip my handrims. On a related note, is there anything that helps you grip better in the rain? I try to just avoid going out in it, but life happens, y'know?

I don't really have any other specific questions (it'll be my first winter since I got my wheelchair (technically second, but I barely went out last year), so I don't know what exactly to expect), but any tips/advice would be greatly appreciated. ^_^

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