
Andulka

if i look back, i am lost
Peter Solarz

shark vs the universe

Janaina Medeiros
d e v o n
hello vonnie
Show & Tell
Alisa U Zemlji Chuda
cherry valley forever
art blog(derogatory)

izzy's playlists!
Lint Roller? I Barely Know Her
I'd rather be in outer space πΈ

PR's Tumblrdome
Monterey Bay Aquarium

β£ Chile in a Photography β£
dirt enthusiast

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@mag139

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HELL
(I wasn't sure how to draw Hell in a really expressive way, so I ended up thinking, "What if it uses the corpses or remnants of V1's defeated enemies as a stand-in for itself?")
something wrong w my copy of ultrakill bro what are they doing
Together Forever
Excited for FRAUD

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Deltarune Fun Fact:
Sometimes a girl will make a noise.
by far the best ad Iβve gotten on this app entirely because I tried rotating it out of sheer curiosity and absolutely nothing happened
When it comes to chronic illnesses, mental illnesses, and disabilities, I've noticed that a lot of able-bodied people either don't take names seriously, or don't understand and ask you to explain what it is to them.
Now, if you have any kind of disability, you know it's fucking annoying go have people make you explain something over and over again, or have people go "oh, you have X? You mean, like the [awful stereotype] thing?"
So, I have realized recently that being Vague As Shit is great for making people leave you the hell alone.
I have autism and anxiety, and with that comes the symptom of selective mutism. If you don't know what that is, Firefox is free. But I had an episode where I couldn't speak today in one of my classes, and knew I would have to explain it to my partner and probably my professor.
This usually goes with me writing that I can't speak, them asking why, me saying selective mutism, and them asking me what that is. Then I have to painstakingly write out an explanation. And, obviously, I'm tired of this. So I tried something new. When he asked, I simply told him I couldn't speak, and when he asked if I physically couldn't or just didn't want to, I just opened my mouth and unleashed the terrifying, awful, broken stuttering that comes out when I try to speak while mute.
His response was "OKAY OKAY OKAY YOU CAN STOP NOW" and he did not question me for the rest of class, and even explained to the professor what was wrong when she tried to make me popcorn read.
This also works on doctors. When I tell doctors I have PCOS, POTS, or hEDS, they usually hear "oh the crazy women self diagnosis disabilities" and treat me accordingly. So, instead I drop unhinged symptoms until they leave me alone.
"Yes, my last menstrual cycle started on December 12th, 2025 and ended January 28th, 2026." "I have experienced several events where I have passed out randomly, yes." "My hip has subluxated six times in the past week."
It's like in the principles of writing horror. If you name and describe the problem, it's easier for people to minimize and ignore. Don't let them. You live with this fucking bullshit every day. Let your symptoms haunt people. They don't need to know everything about you. Besides, it makes them treat you better than when you give them names.
Saw someone on Instagram saying that if you're on T you should take men's multiviatims and if you're on E you should take women's multivitamins. And I can see how someone could come to that assumption, if you thought that vitiam intake needs were affected by hormone levels.
However that's not really the case, at least not when it comes to the sort of vitiams in a multiviatim.
The main difference is that "women's" multiviatims have iron in them to help make up for presumed monthly bloodloss. And "men's" multiviatims will sometimes have antioxidants that /could/ help with prostate health.
If you don't experience a menstrual cycle that features uterine shedding and consist monthly bleeding, then you shouldn't take multiviatims that are marketed as "women's", becouse if you use them longterm you'll end up suffering from secondary iron overload which can cause liver, heart, and pancreas damage.
To my knowledge, the antioxidants in "men's" multivaitims are not harmful to people who don't have a prostate. It's also might be good to remember that trans men on Testosterone for at least a year do develop prostate tissue (it's just not in the same spot). That being said, the antioxidants in men's vitiams aren't medically proven or assessed by the FDA as being beneficial to the prostate tissue - and what studies that do exist certainly don't include transmasculine people in testing, so really it's more π€· π€· π€·
Anyway, basically:
If you're postmenopausal, if you're on T and it has stopped your menstrual cycle, or if you have a condition that makes it so you don't bleed every month, or if you're a trans woman or otherwise transfem then you probably don't want to be taking multiviatims that are marketed towards women, to avoid secondary iron overload.
And if you're on T but you still have a consistent menstrual cycle, you /might/ want to take multiviatims that are marketed towards women to make up for the iron loss during uterine shedding. Though this probably is only necessary if you are a heavy bleeder or someone who bleeds more days then the average.
Now - if you're transfem and having to take multivaitims marketed as "men's" makes you dysphoric, or if you're transmasc and having to take multiviatims marketed as "women's" makes you dyphoria, of it your transneutral and hate any gendered marketing in general. There is good news.
Adult multiviatims, which are marketed as just "for adults" provide a good baseline amount of vitiams that every person needs regardless of gender, with no iron and none of the antioxidants that are sometimes added to men's vitiams.
You can just take those, they're usually cheaper then the gendered ones. And if you think you need more iron, just buy a bottle of iron supplements (talk to yourd doctor or OB/GYN first) or eat more high iron veggies during your period. And if you're concerned about your prostate health then you should talk to a doctor instead of taking an antioxidant about it!
Hey, you, cis girl that's very (correctly) vocal about women being allowed to talk about their periods, do you include trans women in that?
I ask because every single time I've tried to talk about it to anyone that isn't a trans woman they get fucking angry. Which has caused me to have to just suffer in silence every single month. So I really relate to cis women when they talk about literally the exact same thing; being shamed by everyone around them their whole lives for talking about their periods, so they just suffer in silence every month as it negatively impacts their work and social lives. But I don't even feel like I can voice that I am literally dealing with the same exact thing because most of y'all react like you want to throw me in front of a bus for saying it, even those of you who act like your such big great transfem allies.
I guess I'll take this opportunity to talk about trans women periods. The first thing any tme person thinks when they hear this is always "how can trans women have periods? They don't have uteruses!"
The answer is: the uterus isn't what causes your period, it is effected by your period. What causes your period and what causes trans women's periods is the same thing: the endocrine system.
HRT changes the sex of your endocrine system. Feminizing HRT makes it a female endocrine system, giving us a 28-day hormone cycle just like cis women. At the end of that cycle, the hypothalamus floods the body with prostaglandins. Those are what cause all but one of the period symptoms, because they make muscles inflame and contract. They are what make the uterus shed its lining, they are what cause intestinal cramps, they are what cause body aches, they are what cause headaches and migraines. The only period symptom not causes by the release of prostaglandins throughout the body is depression, and that is caused by your endocrine system simply not processing as much estrogen and from simply feeling like shit.
So, the only symptoms trans women don't get every 28 days is menstrual cramps, because yes we do not menstruate since we don't have uteruses. But migraines, depression, body aches, intestinal cramps, and the infamous "period shits" don't exactly add up to us having any better of a time. Except we have to pretend that we're fine and nothing is different because no one believes that we get periods, not even cis women.
"But you can't call it a period then because that refers to MENSTRUATION!" is another one I hear all the time. This is incorrect. You use the word "period" instead of just "menstruation" because it doesn't just refer to menstruation. It refers to a period at the end of the hormone cycle where we experience a host of symptoms. And not all cis women experience all of the symptoms that encompass the period. Not all cis women get migraines, or body aches, or have severe depression. If a cis woman gets a hysterectomy she doesn't menstruate either! In that instance she experiences an identical period to what trans women experience. Yet, I doubt you'd insist that cis women who've had hysterectomies don't have periods.
Oh, another thing that I personally discovered after bottom surgery: vaginal odor changes for trans women during our periods too. I was not expecting that because I always thought it was just from menstruation. But nope, the ph levels of a trans woman's vagina are the same of as a cis woman's vagina, and it changes during our periods just the same.

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I like the idea of Loop's body toeing the line of uncanniness
i love this mod
TW!! Corpses/body horror
Oh boy, I sure love giving minecraft more horror elements, despite me knowing I would be absolutely terrified
Wonderlanding my dot jars or whatever
DON'T TURN LEFT
I love mentions of the King in Yellow in the media. especially in Minecraft Arg.

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
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Gone mining
My take on the Knocker + sona