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(*some photos of tardigrades don't show their eyes because they're 3-d scans of the tardigrade's surface and the eyes are inside of their transparent head)

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pucciverse

time loop fans when the loop changes slightly

idonutdonuts-blog

Time loop fans when the Loop changes slightly

Beauty and the beast au where Jack still has his powers but Pitch does not due to them being sealed away by the beast curse. As a result Pitch can't actually make Jack stay but Jack hangs around anyways. Being a little shit Bonus points for Jack being an outcast because of the magic and appearance change from his lake accident. bonus bonus if the furniture is played by the other guardians

#Rise of the Guardians #Jack Frost #Pitch Black #Beauty and the Beast #writing prompt

glumshoe

imagine Bob Ross painting in the style of Hieronymus Bosch

“this little demon down here is kind of lonely, let’s give him some happy little friends. little demon party.”

snazzystarlight

“Death of a Bachelor” from Panic! at the Disco, as I see it because of synesthesia, a condition that causes me to see music visually.

Done for Doodle Day!

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Selfie game on point??? Or maybe there never was a point, pointy chin?? Pointy glasses

#selfies #actually looking good in a picture #actually feeling positive thoughts at the mirror

chlostars

listen up: “hark the herald angel sing/ glory to the newborn king” and “i know when that hotling bling/ that can only mean one thing” have the same number of syllables

merry christmas

herpowerisherown

WHAT HAVE YOU DONE

evanactually

Omg Rami playing a gay teen in this sitcom is probably the best thing I’ve ever seen.

cold-berry-blog

Aanw mah gawd just watch just !

ofelah

this is so overwhelming

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suspected-spinozist

My favorite ever pronoun story has to be one of my German professor’s. He fondly remembers being mugged by a gang of teenagers in Dresden, who used Sie (formal you) the entire time.

ask-sparkling-awesomeness

HAND OVER THE WALLET MY GOOD SIR

mariberlyn

partially-inkstained

a century in verse.

a project i did for a music history class, connecting the social issues of the time with music

i only messed up a little bit so i’m saying it was a good first attempt at spoken word

incalyscent

seven weeks on testosterone

I don't think we're bad people, we just came from a bad place.

Shame (2011)

#Shame(2011)#what a good movie #thinks of this now

trufemale420

The medical community on literally every female specific health issue ever: “very common condition” “no known cause” “no known cure” :))))))

newtonssidedick

What the fuck is tumblr? Like honestly what is this? Do you guys pull shit out of the inner most depths of your rectum and then just throw it on your keyboard and have it turn into a post???? This site is something else what the fuck is wrong with you people????!?!?

trufemale420

Endemetriosis

Vaginal Thrush

Menorrhagia

Polycystic Ovary Syndrome

Fibroids

Very common conditions, causes are unknown or only speculated, long term cures have not been found. Most can cause chronic pain or discomfort, all can seriously impact your quality of life.

witwitch-deactivated20160508

Men are so damn privileged they can’t even imagine female bodies have different healthcare needs than theirs and that our healthcare needs are important even if they can’t be affected by one of these conditions.

hyggehaven-deactivated20200904

Endometriosis causes excruciating pain and is a leading cause of infertility. Thrush is extremely uncomfortable, and expensive to treat repeatedly; over-the-counter preparations rarely completely eradicate it. Menorrhagia, which I have, makes you anæmic. PCOS causes hormonal symptoms that are socially difficult (facial hair, acne, hair loss, weight gain). Fibroids are so common, and are often treated with a hysterectomy.

Add in fibromylgia, which affects 8x as many women as men, as well as lupus (and almost any other autoimmune condition), systemic exertion intolerance disorder (SEID), iron deficiency anæmia (all of which affect more women than men), and you have well over 25% of childbearing-age women globally living with chronic pain and tiredness.

Chronic pain is overwhelmingly experienced by women, and women are less likely to be taken seriously or given treatment by medical professionals. I went through two years of diagnostics to finally find out I had occipital neuralgia; I felt doubted when I described my pain at every step of the way, but was lucky to have a partner who was persistent in helping me get treatment.

Basically, this is a huge problem, and also one of the reasons I have been considering medical school.

feminerds

Don’t forget that most pharmaceuticals go to market without ever having been tested on people with a uterus, lest someone get pregnant… seriously that is the whole rationale behind not testing >50% of the population. This has been legislated against in some countries, but still persists in the of majority drug development because of other regulations, and traditions and laziness. The use of a drug is of course monitored in the population after release, but the people “trying” it in this capacity get none of the insurance, close and regular medical examination or monetary benefit of essentially being in a late stage drug trial. Drugs that are pulled from market after release are sometimes done so on the basis that the dosage is just too high for females/afab people and this is, of course, after they’ve experienced the adverse affects.

This is why if you get pregnant your doctor will take you off basically any and all medication you’re taking (including mental health medication, can’t imagine any implications/dire consequences there), not because they know it will have an adverse affect on the foetus but because they have no idea. How wonderfully kind of them to prioritise the health and life of an unborn foetus over that of a living person, let’s just hope they don’t become ill whilst pregnant. How charmingly logical it is that they wouldn’t even bother to test drugs in people with a uterus because it’s all too difficult and gosh, darn what an ethical conundrum we’ve been faced with, let’s just not! Which is so in the spirit of capital S, Science!

Sources: Nature, Nature, Medscape, Biomedcentral.

prokopetz

Indeed, the issue is so severe that, in many cases, folks with uteruses are routinely told that their diseases and disorders are not, in fact, disorders at all, and are just a normal part of having a uterus.

Take menstrual cramps, for example. Everybody knows that cramps are a normal part of menstruation, and that virtually all people who menstruate experience them throughout their lives, right?

Except that’s not right at all.

Yes, it’s true that about two-thirds of individuals who menstruate begin to experience menstrual pain during adolescence, but it’s basically a side effect of puberty, and normally subsides by your late teens. Only about 20-40% of menstruating adults experience menstrual pain on a regular basis - and according to some estimates, as much as 80% of that figure is due to undiagnosed endometriosis or some other underlying medical condition.

Yeah, roll those numbers around in your head: if you’re an adult who experiences menstrual cramps, it’s overwhelmingly likely that your pain is a symptom of some potentially serious medical condition.

And yet we tell folks it’s just a normal thing that everybody has to deal with.

dottewa-deactivated20200728

Bonus round: Look up PCOS and gender identity.

Then look up PCOS and diabetes.

thepageofhopes

Ok, to show how incredibly important this post fucking is, I just looked up endometriosis and I match just about every sympton, and it would explain not just my incredibly painful periods but many other things as well. I had no idea this existed. Please, read this post and reblog this so others can learn.

philosopher--queens

I will reblog this every time because my cousin (a cis girl) went through seven years of pain without being taken seriously until SHE suggested it was endometriosis. And that’s not even unusual - that’s the average amount of time it takes between first symptoms and a diagnosis of endometriosis.

wickedkhaleesi-blog

NO KNOWN CAUSES OR CURES. JUST SUFFER. - the doctors diagnosing me with pcos, Fibromyalgia, and endometriosis.

dynastylnoire

I was diagnosed with endo when was in my early twenties. Their advice to me was hurry up and make babies because you could be made infertile.

Go on birth control

Or have a hysterectomy

Something else to know is endo spreads. So you can get misdiagnosed for everything but endo because of the location of your pain.

My endo spread to my navel, gallbladder, rectum, ovaries, and vagina. The gallbladder pain caused my side to burn. Went to the er for it 4 years ago and they told me it was acid reflux

When my navel started bleeding when I was at work last fall er docs told me if was an infection.

In both cases I said I have endo but the endometriosis causing these symptoms was ignored until I went to a specialist.

cantcolonizethispussy

i’ve had endometriosis and pcos most likely since i was 15-16 years old. i was already infertile by the time i was finally diagnosed with both at 23. i’m 25 now and JUST started being treated for it. i went to doctors for years who didn’t take any of my symptoms seriously and tried to convince me over and over again that my symptoms were nothing to worry about, that it was totally normal to be having excruciatingly painful periods that prevented me from getting out of bed for days and that there was nothing that could be done. i’ve gone to the ER and have had doctors give me painkillers because my periods were so painful. before i knew i was infertile there was a time i thought i had a miscarriage and maybe just didn’t know i was pregnant or my appendix had ruptured because it was so bad. now i’m waiting for my doctor to figure out if i have fibromyalgia because there’s no actual test for it. these are only a few amongst a host of other health issues i have now, many of which developed from undiagnosed + untreated endometriosis and pcos. it took me over 10 years to find a doctor who is listening to me and taking all of my concerns seriously.

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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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mondoes-deactivated20150506

horse people are spectacular to listen to bc they love to go on about the “trust” between horses and people and it’s just enchanting. I leave that conversation completely mesmerized by the idea that a person actually trusts one of those fucking demon creatures when you can see it on their face that there is no life or love in their eyes. horses are the ready vessels of a vengeful, hateful god and we should leave them to eat the fucking ground in peace

tangelojack

@partially-impartial

The thing I hate most about depression is that it tricks you into thinking you don’t have depression. It makes you think that nothing is wrong with you, that you just feel this way because you lack value as a person. Whether that’s in your relationships, your academics, or a view of yourself, it makes you think you aren’t good enough for any of that.

“It’s not the illness,” it says, “You feel this way because it’s who you are.”

adhdedrn

“Mental illness is like fighting a war where the enemy’s strategy is to convince you that the war isn’t actually happening.”

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