Liam/Gray. 18. They/them.
I am a student, occasional filmmaker, and general stuff enthusiast. And things. I am good at being specific.
NO “TELEPHONES”. TALK TO EACH OTHER. FACE TO FACE ONLY. WRITE A LETTER. SEND A TELEGRAM TO YOUR MOM. PRETEND IT’S 1860. LIVE.
NO ‘WRITING’… TALK TO EACH OTHER. THROW A ROCK AT YOUR MOM. PRETEND IT’S 10,000 BCE. LIVE.
URGGA. ROU GRAAURH. RUH.
<SMACKS HANDS ON WALL WITH PAINT.>
NO ‘HIGHER BRAIN FUNCTIONS’ …USE YOUR REPTILIAN BRAIN
EAT YOUR MOM’S CORPSE SHE DIED TO PROVIDE YOU WITH SUSTENANCE
PRETEND YOU HAVE JUST AROSE FROM THE SEA
NO “MULTICELLULAR TRAITS”….. USE YOUR SYMBIOTIC MITOCHONDRIA
REPRODUCE ASEXUALLY, YOU’RE YOUR OWN PARENT
PRETEND IT’S 2BYA
NO “LIFE.” USE FUNDAMENTAL PHYSICAL FORCES TO FORM SPHERICAL OBJECTS REVOLVING AROUND ONE ANOTHER IN SPACE.
FUSE HYDROGEN INTO HELIUM USING GRAVITATIONAL PRESSURE TO PRODUCE HEAT AND LIGHT.
PRETEND IT’S 4.5BYA.
STABILIZE INTO EQUILIBRIA
NO “MATTER”. EXIST IN THE VOID WITHOUT PURPOSE OR MEANING.
THERE IS NO “YOU”, ONLY THE VAST CONCEPT OF NOTHING.
TIME DOES NOT EXIST.
I feel like something really important just happened
Confused husky pup
He’s not expressing confusion, he’s tilting his head for better sound localization. While having an ear on each side of the head is good for lateral echolocation, tilting the head so that the ears are offset gives it vertical depth.
Thank you dog side of tumblr!
Today’s picture for invisible illness is a personal one. This is one of about 30 notes that my friend has received since using her handicapped placard. I’m going to say this to you, have you ever seen someone get out of a car parked in a handicapped space and said to yourself “they look too young or they don’t look disabled.” I’m going to go with yes you have, because we all have at one time. I can’t remember doing it, but before I understood the difficulties of invisible illness when I was younger I probably did. Let me ask you this though, when you had that thought was it because you knew with 100% certainty that they weren’t handicapped or did you assume that because of their age and/or not seeing a cane, walker or wheelchair? All I’m asking is that we stop and think when we someone need a mobility aid, park in a handicapped space or say they are disabled that we remember this “DISABILITY HAS NOTHING TO DO WITH AGE OR APPEARNACE.” #spoonie #invisibleillness #disability #chronicillness #rheumatoidarthritis #lupus #fibromyalgia #myofascialpainsyndrome
If nothing else, this post needs to be seen around the internet more. This harassment is not okay and no one should have to deal with it on top of having an invisible illness. This is just another form of anonymous bullying to add to the internet bullying these TROLLS are capable of.
If you are healthy, please reblog.
If you are sick, please reblog.
If you have a disability, please reblog.
If you have an invisible illness, please reblog.
If you know someone with a disability, please reblog.
If you are a human being, please reblog.
Let’s spread the word and help those of us that may not look like it.
Ignorance isn’t bliss, ignorance is ignorance.
But you have to understand that when both my cousin and I came out as bisexual to our great-aunt, she told us we were too young to label ourselves.
You have to understand that both of my brothers are gay and came out to her before the ages of 15. She had absolutely no problem.
My great-aunt is a 69 year old lesbian.
You have to understand that not every aspect of biphobia has to do with homophobia.
Uh…… you mean like this?
wow. let it be known that tumblr legitimately changed my opinion on something today.
I’m sorry but is there an advert about toilet paper in there. They are legitimately trying to sex up toilet paper.
I always felt uncomfortable and angry looking at these stupid adverts, glad I’m not alone.
“Just so everyone is aware, there is a bunch of misleading info being spread around re: ALS research - the “27%” figure is based on previous years’ annual funding; furthermore, the remainder goes to improving the quality of life of those suffering from ALS. Given that the annual funding is approximately 16M, that’s just over 4M spent on decreasing their suffering. It isn’t greed, it’s a lack of money.”
Shut up already.
And the next time you start to complain about a charity either a) working on multiple fronts (because that’s what ALSA does—both seeking a cure and helping people suffering now) or b) daring to have administration expenses—let’s see how long you can last, much less tackle a cause, without printer paper and an internet connection.
As someone who has watched a family member die from a neuro-degenerative disease; funding to develop better wheelchairs and bedsore creams is *just* as important as funding research to cure the disease itself…
A friend of mine posted an update from one of HER friends to FB earlier. Her dad has ALS. The ALS foundation came out to see if they could put in a ramp for his wheelchair, but they couldn’t afford it because of the kind of ramp he needed for the kind of house they had.
This week they called back and said hey, the thing is, we suddenly have a bunch of money, so we’re coming out to build that ramp. And they did. She posted pics.
So if you feel like bitching about the ice bucket challenge…reconsider.
hi so my friend alice has been missing for over 24 hours now and everyone is getting really worried, so if you live around london uk would you please ring 101 if you see this girl, it would mean a lot thank you bye
http://www.bbc.co.uk/news/uk-england-london-28997068 this bbc news story explains more about it so please help if you can #findalice
Please help find Alice - west London - URGENT help needed
PLEASE SIGNAL BOOST THIS
she was last seen in Kew by the canal, but she could have walked anywhere from there
shes only 14 and has health problems that make her seriously vulnerable
another pic of her:
REBLOG YOU NEVER KNOW IF ANY OF YOUR FOLLOWERS MAY LIVE IN WEST LONDON AND KNOW SOMETHING THAT COULD HELP
Since the TFIOS movie became available On Demand and for digital download and people can now pause and zoom in and stuff, many people have asked who wrote the pages of An Imperial Affliction that appear in the movie.
I did. Executive producer Isaac Klausner asked me to write four pages (the two you see here and the final two pages of the book) for the movie edition of An Imperial Affliction, so I did. In this passage, Anna is recalling intense pain breaking through her high doses of narcotic pain medication.
The book that Hazel reads in the movie is just the four pages I wrote printed over and over again hundreds of times. I have a copy of it in my house; it’s my only souvenir from the movie set.