my teen angst bullshit has a body count
dani. seventeen. ♌. infp. slytherin. perpetually annoyed queer. feminist. broadway enthusiast.








the more i think about it, the weirder this comment seems. how does this man know that being a male lion is more stressful than being a female lion. has he lived as both a female and male lion before. is this man an Animorph


male lions rights activist

as a big cat fanatic and a zoo veteran: 

male lions are lazy fucks. they CHOOSE to fight cos they’re BORED.

As a professional Ethologist who specializes in apex predator and primate behavior, I can fully support this lazy lion notion.
See this gorgeous guy? 

This is Zero, the most photographed lion in National Geographic history (so I’ve been told). While his huge frame and two-toned mane make him an intimidating sight, he is essentially the biggest baby I observed while in South Africa.

You would hear these deep roaring moans echo across the reserve… and it was Zero, whining for the girls (Maggie and Lisa) to bring him food. The lazy bum would just roll around in the river bed moaning and groaning until the females would show up with a kill. 

Sure, he could fight if there happened to be a rival male in the area. And his ‘mock charge’ display was intimidating enough to keep just about everyone* out of his way… but 99% of the time this guy was all about moaning (for food), mating, and mane-flips.

* - The only animal not run off by Zero’s display was a honey badger, who - true to form - did not care.

(via nordvrai)



still havent seen any greenday jokes….its september….wtf is going on

i guess everyone’s on holiday

(via peggycarterslipstick)


When MLK said “I they will not be judged by the color of their skin, but by the content of their character" he was saying that ‘I hope one day that i can walk down the street without being stereotyped and killed’

Why would he be talking about white people.

In what world would be trying to fight for “white rights” or for white people to be treated ‘equally’ when they already had a majority of the power, what fucking sense does that make.

(Source: blastortoise-chan, via princessquinne)

#queue sera sera


imagine banana with any other vowel






(via fondueit)

#queue sera sera



remember gotye

now he’s just somebody that we used to know

(via danielamoreiraa)

#i miss gotye #does he even make music anymore #bc his other stuff was great
want my origin shit?

oh wow if it’s not too much trouble!

#heatherchandlersscrunchie #replies

endless list of favorite characters → katniss everdeen, the hunger games

The bird, the pin, the song, the berries, the watch, the cracker, the dress that burst into flames. I am the mockingjay. The one that survived despite the Capitol’s plans. The symbol of the rebellion.

(via skiestintedorange)

#q'orianka kilcher as katniss IS MY FAVE #thg

does anyone have a torrent of sims 4 that works or st bc that would be great

#i just want to play it for like an hour #there's no way i'm paying $70 for something i might not even like


if you threw a pad or tampon into a crowd of boys they would probably all scream and it would be like that scene from monsters inc where george gets contaminated by a sock

(via new-newdoctor)

#queue sera sera

Olivia, my eldest daughter, caught measles when she was seven years old. As the illness took its usual course I can remember reading to her often in bed and not feeling particularly alarmed about it. Then one morning, when she was well on the road to recovery, I was sitting on her bed showing her how to fashion little animals out of coloured pipe-cleaners, and when it came to her turn to make one herself, I noticed that her fingers and her mind were not working together and she couldn’t do anything.

“Are you feeling all right?” I asked her.

“I feel all sleepy, ” she said.

In an hour, she was unconscious. In twelve hours she was dead.

The measles had turned into a terrible thing called measles encephalitis and there was nothing the doctors could do to save her.

That was twenty-four years ago in 1962, but even now, if a child with measles happens to develop the same deadly reaction from measles as Olivia did, there would still be nothing the doctors could do to help her.

On the other hand, there is today something that parents can do to make sure that this sort of tragedy does not happen to a child of theirs. They can insist that their child is immunised against measles. I was unable to do that for Olivia in 1962 because in those days a reliable measles vaccine had not been discovered. Today a good and safe vaccine is available to every family and all you have to do is to ask your doctor to administer it.

It is not yet generally accepted that measles can be a dangerous illness.

Believe me, it is. In my opinion parents who now refuse to have their children immunised are putting the lives of those children at risk.

In America, where measles immunisation is compulsory, measles like smallpox, has been virtually wiped out.

Here in Britain, because so many parents refuse, either out of obstinacy or ignorance or fear, to allow their children to be immunised, we still have a hundred thousand cases of measles every year.

Out of those, more than 10,000 will suffer side effects of one kind or another.

At least 10,000 will develop ear or chest infections.

About 20 will die.


Every year around 20 children will die in Britain from measles.

So what about the risks that your children will run from being immunised?

They are almost non-existent. Listen to this. In a district of around 300,000 people, there will be only one child every 250 years who will develop serious side effects from measles immunisation! That is about a million to one chance. I should think there would be more chance of your child choking to death on a chocolate bar than of becoming seriously ill from a measles immunisation.

So what on earth are you worrying about?

It really is almost a crime to allow your child to go unimmunised.

Roald Dahl, 1986

(via brain-confetti)


(via watchoutfordinosaurs)


roald dahl was calling out the anti-vaccination movement as self indulgent bullshit //thirty god damn years ago//.

(via ultralaser)

Over 1,000 preventable deaths and 128,000 preventable illnesses since 2007 and counting

And this is only in recent history. I can’t imagine the numbers if we had data all the way back to 1986.

(via autistiel)

And thanks to anti-vaxxers, measles is back in the United States.

(via thebicker)

(via punkassbookjockeys)


I ship myself with academic success and contentment

(via kiracompton)

#about me

Autism Speaks Masterpost (new! Updated 6/20/14)


Trigger warnings for ableism, abuse, autistic “therapy”, discussion of a cure, discussion of murder, eugenics, the way Autism Speaks uses their research, etc.  All of this is under a cut.  Be forewarned. 

When a person thinks of the term “Autism Awareness” in the United States, it’s usually one organization that comes to mind - Autism Speaks.  It is heralded by celebrities, politicians, nonprofit and for profit organizations alike. Many parents of autistic children enthusiastically applaud their “efforts”, even partaking in fundraising, despite not knowing much about what those efforts entail.

 Ask an autistic person, however, and you might get quite a different picture of Autism Speaks.

 The number one tenet of any activism among disability groups is “Nothing About Us Without Us”, yet Autism Speaks can’t even manage to meet this one basic qualification.  They have never had an autistic member on their board.  Their current board consists of parents, including one who founded SafeMinds, which has contributed to the anti vaccination movement, as well as another board member who used be a board member for Cure Autism Now. To view the full list, click here. To view a list of other leadership in their organization, click here.

The only autistic person high enough up in their leadership to be worth mentioning was John Elder Robison, author of Look Me in the Eye: My Life with Asperger’s Syndrome and part of their science advisory board.  He resigned his position in November 2013, a decision he spoke about on his blog.  

Autism Speaks spends just 3% of the money they raise back into helping families and autistic people.  This comes in various forms, and not all of it is aimed at actually helping autistic people.  Some of it is aimed at communication devices for autistic children and teenagers, and this is of course a very good thing.  Much of it is also aimed at providing ABA therapy for autistic people, which is a behavioral intervention that much of the autism community opposes, particularly autistic people who are now adults who were subjected to it as children.  Some accounts of this are hereherehere and here.

 Autism Speaks’ goals are clearly stated in their mission statement.  It reads:

At Autism Speaks, our goal is to change the future for all who struggle with autism spectrum disorders.

We are dedicated to funding global biomedical research into the causes, prevention, treatments and a possible cure for autism. We strive to raise public awareness about autism and its effects on individuals, families, and society: and we work to bring hope to all who deal with the hardships of this disorder. We are committed to raising the funds necessary to support these goals.

Autism Speaks aims to bring the autism community together as one strong voice to urge the government and private sector to listen to our concerns and take action to address this urgent global health crisis. It is our firm belief that, working together, we will find the missing pieces of the puzzle.

I have bolded the parts that stuck out to me as harmful and problematic.  Autism Speaks wants to cure autistic people of our autism.  Have they involved us in the process? Have they asked any of us? Again, the guiding principle of the disability rights movement is “Nothing about us without us”, but Autism Speaks has left autistic people out of the equation entirely.  In addition, it’s clear to see when perusing their scientific research that much of the research is focused on identifying genetic markers for autism, presumably so that autism can be prevented.

Is autism an “urgent, global health crisis”?  I don’t believe it is.  Studies have shown that there is a similar percentage of adults that show the same symptoms of autism as is shown among children currently being diagnosed with autism.  Link here.

The above mission statement is indicative of a larger problem in the way that Autism Speaks speaks about autistic people.  

  • Autism Speaks is responsible for the atrocity known as I Am Autism. Directed by Alfonso Cuaron, this promotional video utilized a disembodied voice to tell the audience what precisely “autism had stolen” from the families of autistic children, even citing divorce as a result of autism, likely relying on a now disproven statistic that 80% of marriages in which there is an autistic child end in divorce.  Neither Cuaron or Autism Speaks has ever offered an apology for this monstrosity, though they did remove it from their YouTube channel.

  • Autism Speaks is responsible for another media piece called Autism Everyday.  There are several issues with this video.  The parents spend most of the time talking about what they cannot do with an autistic child.  They cannot go out for coffee with their friends, they cannot do x, y, and z, because their child is autistic.  The conversation seems to be only focused on what the parents’ lives are like, and there is almost no discussion on how it feels for the autistic child themselves.  The worst part of this video, however, is when Alison Singer, former Autism Speaks board member and founder of the Autism Science Foundation, speaks about her desire to drive her daughter and herself off the George Washington Bridge, and only stopped because she was thinking of how it would affect her non-autistic daughter.  The heartbreaking part of this is that she says all of this in front of her autistic daughter, with no regard as to whether her daughter can hear and understand.  

  • Autism Speaks often refers to autism as a “puzzle”, making use of a human-shaped blue puzzle piece in their logo.  The puzzle piece did not originate with Autism Speaks, but their continued use of it, in addition to phrases like “…will find the missing piece of the puzzle” as stated in their mission statement shows that they don’t really value autistic people as fully human people.  We are puzzles and we are missing pieces of ourselves, and we must become neurotypical in order to be respected by this group.

  • Suzanne Wright, one half of the founding team of Bob and Suzanne Wright, who founded Autism Speaks in 2005, focuses her “founder’s message” on speaking about the ways to supposedly help the families of autistic people, with little discussion of how to help autistic people ourselves.  She concludes this message with the phrase “This disorder has taken our children away.  It’s time to get them back.”  

  • Jess, a blogger and mother of an autistic daughter, who blogs at A Diary of a Mom, detailed her encounter with Suzanne Wright and Autism Speaks here. This details everything that is wrong with ABA therapy, lack of consent, as well as just having no idea how to relate to an autistic child.  The fact that Suzanne Wright was one of the first voices of an organization such as Autism Speaks, while having no idea what consent even means, is horrifying.

Autism Speaks has been involved in legislative issues, and while many people would consider this to be a positive effort, the effect this has on autistic people is actually quite negative.  

As stated previously, they have members of their board who are very concerned with environmental factors (such as vaccines) and how they contribute to autism diagnoses.  Autism Speaks was, for quite a long while, very much anti vaccination.  Alison Singer left Autism Speaks in 2009, no longer wanting to be a party to an organization that wanted to spend so much on researching vaccines, a link that has long been disproven.  

Autism Speaks, among other groups, blocked the inclusion of the Shakowsky Amendment in the recent Autism CARES ACT, which would have included some of the following:

  • A requirement that the Leadership and Education in Neurodevelopmental Disabilities (LEND) program, a federally-funded training program to provide interdisciplinary training to students seeking to support children and youth with disabilities, take steps to recruit trainees on the autism spectrum and those with other developmental disabilities;

  • Specifically emphasizing the needs of racial and ethnic minority groups, women and girls and adolescents and adults on the autism spectrum in the definition of “culturally competent services”;

  • A requirement that autistic people make up at least four of the public members of the Inter-Agency Autism Coordinating Committee or one-third of the public membership, whichever number is higher, and that at least one such individual be a person who has received Medicaid Home and Community Based Services;

  • A requirement that LEND programs convene stakeholder advisory committees consisting of a majority of individuals on the autism spectrum or with other developmental disabilities;

  • Opening the Autism Centers of Excellence research funding stream to include research on developmental disability service provision, supported employment, inclusive education and other fields related to the integration of autistic people into the broader community; and,

  • A requirement that each Autism Center of Excellence grant awarded include a stakeholder advisory committee with a majority of individuals on the autism spectrum.

Autism Speaks has also allied themselves with the Judge Rotenberg Center. If you don’t know what the Judge Rotenberg Center is, it is an institutional that routinely uses electroshock on autistic people as punishment for even minor infractions.  Here are a few links for more information.  x x x Please read all links with caution.  This is a gruesome practice, and the fact that Autism Speaks is offering such an organization a place at one of their resource fairs, as a potential resource for parents of autistic children is quite alarming.

Autism Speaks has recently teamed up with Google for the Ten Thousand Genomes Project, also known as AUT10K.  The major issues with this project are mentioned at the link, but they include questioning Autism Speaks’ intentions with the information as well as ethical and privacy concerns .  Some information regarding autistic people’s rights with regard to genetic testing can be found here.

A short list of a few other notable failures of Autism Speaks:

  • Autism speaks has plagiarized/violated the copyright of an autistic adult.

  • Autism Speaks shared the news of Google removing hate speech regarding autistics from Google’s autofill feature, completely erasing any mention of autistic people’s flashblogs having anything to do with the change.  It was only after a member of the autism community (and not a parent, but an autistic person themselves) spoke with a reporter about the flashblog and a statement was released to the media that Google decided to make this change.

  • This woman’s job offer was rescinded after she asked Autism Speaks for accommodations in caring for her autistic son.  They refused, and she made necessary accommodations for childcare, but they withdrew her offer anyways.

  • Autism Speaks has threatened at least two autistic teenagers with lawsuits over legal parodies.  Here and here.

  • Autism Speaks has reported on the murders of autistic people by their parents/caretakers, but has never reported said facts without somehow pointing to “lack of resources” as a reason for such tragedies, as well as continually ignoring their own possible culpability in these crimes.  One example is the attempted murder of Issy Stapleton. The more negative rhetoric there is about autism, the more people will dehumanize autistic people to the point that autistic people become a list of behaviors instead of actual people with emotions and needs.

  • Autism Speaks often utilizes functioning labels when speaking about autistic adults.  They use the numbers of so-called “high functioning” autistic adults to prove that autism is an epidemic, but refuse to listen to anyone they deem as high functioning (essentially, anyone who can use a computer).  They incidentally also ignore people they deem as “low-functioning”, because they refuse to presume competence.  Here is a lovely message written by a nonspeaking Autistic advocate, Amy Squenzia.  In addition, here is why you should not be using functioning labels (or tell me how “high functioning” you think I am because I am able to type this document).


Interested in learning more?  


Want to support autistic people? Here are a few worthy organizations/groups/pages.

(via the-exercist)

#long post #important



this is your daily reminder to not forget about ferguson. Keep it going!

S E R I O U S L Y.

(via skiestintedorange)



the fucking worst is when people are like “you hate people for having a different opinion than you!!!!” like im not shitting on this guy because he thinks pistachio ice cream is gross im shitting on him because he actually believes that i and people like me dont deserve basic human rights and respect and safety

(via carewolves)

#queue sera sera


I see girls on this website fighting battles with their disorders and they’re working so hard and they’re so young and I’m like you go little warriors, you get this shit squared off and go to college or Europe or the bar near your house free of all this crap. You’re working so hard to make this a tiny chapter of your story and I am so proud of you.

(via weight-a-second)