urbnbullshitters:

The Kaonashi No-Face Piggy Bank is a money box that automatically takes your coins and saves them for a later date. Place a coin in Kaonashi’s red bowl and then the spirit will “swallow” the money as music plays from the movie (and he even finishes it with a burp). A must-have for Ghibli fans.

Get it HERE

I had a dream recently…

banzai-jinto:

vultureculturecoyote:

That I was out playing pokemon go, and people all over the world had started seeing this new pokemon popping up. Like out of nowhere this little thing started appearing occasionally. No word from Nyantic or The Pokemon Company about when or why they had released it. The pokemon was called “sleepytired” and it looked like this.

And you couldn’t catch it, the ball would just go straight through it. People were data mining and shit trying to figure out how to catch this thing but they couldn’t. Eventually they would just have to give up and leave the encounter. 

After a few weeks of people reporting sightings of it, and no word from Nyantic, some creepy shit started happening…

What started happening was, if you entered an encounter with a “sleepytired” with the AR on it would manifest in the real world. But it wouldn’t do anything. It would just float there, watching. 

So people being curious started doing this whenever they could, and these things would just manifest and stay there. Obviously this was causing problems because these things would just be floating menacingly in local parks and in the local McDonald. And they couldn’t be moved, because anyone who tried to move them or touch them would be struck by sudden, intense, chronic fatigue that seemingly had no cure. 

The last part of the dream I remember was watching a news broadcast telling people that pokemon go was now illegal, and to avoid touching or disturbing the creepy little things that are now just about everywhere.

what, in no particular order, the fuck

Concept: Sirius convinces the Marauders to do a “Family Portrait” in their animagus form.

winnie-the-patton:

vanscribbles:

killerqueen2319:

l0vegl0wsinthedark:

mezzoaribg:

wizardtowizard:

  • Except for Remus, obviously.
  • So Remus is the one human who has to go into the photographer and ask for the picture.
  • Remus is a mixture of embarrassed, exasperated, and amused.
  • “Hello, yes, I’d like to take a picture with my, er, pets.”
  • And this photographer is just astounded that Remus has these very manageable and obedient pets.
  • In all fairness, it’s a VERY good picture.

I want to see this picture

Me too tbh can some giving soul draw this

SOMEONE DRAW THIS PLEASE

only because you said please, although its a very shitty drawing

IT IS NOT AND JAMES HAS GLASSES!!!! ❤ ❤

khealywu:

philosopher–queens:

thepageofhopes:

dottewa:

prokopetz:

feminerds:

hyggehaven:

witwitch:

sweetpotatodotcom:

newtonssidekick:

sweetpotatodotcom:

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

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????!?!?

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.

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.

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.

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.

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.

Bonus round: Look up PCOS and gender identity.

Then look up PCOS and diabetes.

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.

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.

Only 20-40% of menstruating adults experience cramps???? Fuuuuuck >:[