The idea to display the pets inside the store started in Singapore as a collaboration between Ikea and two animal shelters, according to Business Insider. Together they formed the project Home for Hope.
The coolest optical illusion you will see today
Sarah Schönfeld - All You Can Feel
"Since the 1950s, we in the western world have increasingly come to understand our most intimate desires and experiences as the products of a so-called ‘chemical self’. We can explain moods, angers and diseases both physiological and psychological as an imbalance of substances in the body.
All of this, of course, takes place against the backdrop of a constantly shifting legal and political climate regarding the regulation of different types of mood-altering substances.
What do all these substances actually look like when their essence is visually depicted?
Schönfeld squeezed drops of various legal and illegal liquid drug mixtures onto negative film which had
already been exposed. Each drop altered the coating of the film.
Much like the effect of some of these substances on humans, this can be a lengthy process – sometimes one that can barely be stopped.
She then enlarged these negatives including the chemical reaction of the particular drug, to sizes of up to 160 x 200cm.”
4. Crystal Meth
8. Pharmaceutical Speed
The literal negative effects of drugs (on negatives)
A lesson on premature celebrations.
Body paint artist Emma Fay transforms models into stunningly realistic animals. Here, we look at how she did it
Photos: Emma Fay/Barcroft Media
Open Mike Eagle - ”Qualifiers (Live from the Laundromat)”
It takes a special kind of rapper (and person) to make music that revolves so heavily around intelligence and irony without completely alienating his listeners. Open Mike Eagle’s secret? Even when he’s throwing around obscure literature references or crafting two-minute-long figurative satirical narratives or wryly criticizing modern reliance on technology, Open Mike never loses track of himself. Most of his criticisms come tied with a high-profile asterisk: Open Mike Eagle is just as tied to his surroundings and haunted by his demons as each of us, and that grounds his music and casts it in a subtly but crucially different light. These aren’t the superior chastisements of a rapper who knows better than us; Open Mike is just as mired in 21st century faults as each of us are.
Equally capable of carrying his songs by way of rapping and by singing (and of making us laugh and cry), “blending genres” doesn’t give Open Mike Eagle enough credit for what he’s done with Dark Comedy. He’s got a unique knack for phrasing age-old rallying mantras in ways that are both funny and undeniable in their clarity (“Nah, I’m in the hood hearing sirens/And the beat tried to make me feel good but it’s lying” — “Sadface Penance Raps”): as a matter of fact, run down the album’s tracklist for a good sense of Dark Comedy’s unique brand of honesty and irony: “Thirsty Ego Raps” and “Golden Age Raps” slide into “Very Much Money (Ice King Dream)” and the Hannibal Burress-featuring “Doug Stamper (Advice Raps),” while “A History of Modern Dance” makes an appearance later on.Making fun of people without alienating them is a difficult task, and one that Eagle takes to with aplomb.
It says it all, really, that one of the album’s most memorable tracks is about Open Mike being invited to a dream gig on the moon — a show that he has to withdraw from because, well, it’s his wedding anniversary (“Jon Lovitz (Fantasy Booking Yarn)”). That type of wry “well, what can ya do” juxtaposition is what makes Open Mike’s music so powerful; reality is always there to be grappled with, and he’s got no patience for anyone unwilling to confront its ugliness or place their perceptions in question. He might put it best himself on “Qualifiers”: “Fuck you if you’re a white man that assumes I speak for black folk/Fuck you if you’re a white man who thinks I can’t speak for black folk.” Sharp and incisive, Dark Comedy is rap made for today’s society, and Open Mike Eagle is a rapper made for its denizens.
i promise i didnt write this.
On May 28th, my sister, Edna, turned 31.
Her mental age is about three years old. She loves Winnie the Pooh, Beauty & the Beast, and Sesame Street. Even though the below picture is unconvincing.
Edna and “Cookie.” I think she was trying to play it cool.
My name is Jeanie. I’m Edna’s younger sister. I’m also her guardian and caregiver.
That’s me on the left. (Hey, you never know. After a year of writing a blog about online dating - Jeanie Does the Internet - I’ve come to learn that there are A LOT of fools on the internet.)
ANYWAY, I’m not “doing the internet” anymore. I’m taking care of Edna full-time, after completing my MFA in Writing for Screen & Television at USC.
May 16, 2014. I wanted a picture. Edna wanted breakfast.
In case you’re wondering where our parents are, they’re dead. Our mom died of breast cancer when she was just 33.
Us with mom before she died. (Obviously.)
As for our dad, he peaced-out around the time my mom got sick. His loss - we’re awesome.
Here we are being awesome at the beach. Pushing a wheelchair in the sand? Not so awesome.
In case you’re wondering “What’s wrong?” with my sister - as a stranger once asked me on the street - NOTHING. Yes, Edna has a rare form of epilepsy - Lennox-Gastaut syndrome - but I don’t know if that’s anymore “wrong” than people who don’t have manners.
Basically, Edna was born “normal,” and started having seizures as a baby. They eventually got so bad that they cut off the oxygen to her brain, causing her to be mentally disabled. Or impaired. Or intellectually disabled. Or whatever you want to call it - except “retarded,” because in 2010, President Obama signed Rosa’s Law into effect, replacing that word with “intellectually impaired.”
Which is cool and all, but services for the disabled and the people who care for them are SEVERELY LACKING. Also, there’s a bunch of people working in taxpayer-funded positions who are supposed to help families like us, but don’t. (Big surprise, I know.) They just fill out paperwork (whenever they feel like it) with asinine statements like this:
YUP. I transport my sister down the stairs in her wheelchair, because that is not only safe, but TOTALLY PRACTICAL. Why doesn’t everyone in a wheelchair just take the stairs, for God’s sake? Stop being so lazy, PEOPLE WITHOUT WORKING LEGS!
But, as it says above, Edna’s legs do work. Whether or not she wants them to, is another story.
Edna refusing to go inside.
These are the stairs that I have to carry her up - by myself - on a daily basis. That is, until one of my legs break and both of us are just sitting at the bottom of the stairs, helpless.
For six months, I have begged - BEGGED - the State of California to help my sister, which they are required by law - The Lanterman Act specifically - to do so. But they’ve told me “these things take time” and that I “need to amend my expectations.” (That was said to me when I refused to place Edna at AN ALL-MALE CARE FACILITY. Because yes, that was an “option” that was offered to me.)
Prior to Edna moving in with me in my one-bedroom apartment, she was living with her amazing caregiver, Gaby, back in Tucson, where we went to high school and I did my undergrad. Edna’s reppin’ the Wildcats below.
But back in November, Gaby also died from breast cancer. (FUCK YOU, BREAST CANCER!) This picture was taken a month before she died. She never even told me she was sick because she didn’t want me to worry.
By the way, we were raised by our grandma. Edna and her were very close.
She’s dead, too. Surprise.
She died when I was 20 and Edna was 21. That’s when I became Edna’s legal guardian and Gaby stepped into the picture to help me out with Edna.
So, six months ago, after Gaby died, I moved Edna to California, where I tried to get the folks over at The Frank D. Lanterman Regional Center to help me. I’ve told them I’m worried about our safety - that one of us could get hurt on the stairs - I’ve told them I can’t afford to pay the private babysitters $15/hour because the ones social services sent me who make $9/hour were unreliable (they didn’t show up on time or at all so I could get to school and work), untrustworthy (one of them let Edna go to the bathroom in the kitchen and then took her into the bathroom because “that what I thought I was supposed to do.”)
But the people over at the FLRC don’t return my calls, they don’t file the paperwork on time - and the first caseworker that was assigned to us actually LAUGHED AT my sister when he came to our home to evaluate her. When I reported him to his supervisor, she told me, “That’s just [insert name of said jackass].”
He was one of the two caseworkers that contributed to the report I mentioned above, which also included this:
So let me get this straight - I have to feed, bathe, dress and help Edna in the bathroom and you can’t deduce whether or not she is able to vote? What in the fuck?!
Now I realize I seem angry. And you can bet your balls I am. I’m also sad. Sad for those who don’t have family to stick up from them and who waste away God knows where, monitored by no one. Or monitored by people who physically and sexually assault them.
I’m also sad for the caregivers who are SO EXHAUSTED - trying to take care of their loved ones - while also trying to take care of themselves and battling a system that is supposed to help, but does nothing of the sort. And I know a lot of people give up. They let their dreams, their marriages, their friendships slide. All while trying not to resent the very person you’re doing it all for.
Edna wanted to sit next to me the other day while I was writing. Clearly, she’s not impressed.
Here’s the thing: I REFUSE TO GIVE UP. I’M NOT GIVING UP ON HER OR MYSELF. I’m going to pursue my dreams while taking care of her, AND while ensuring that the people paid to do their jobs ACTUALLY do them.
That’s where you come in. I need you to help me get my story out there. Because I know I’m not alone in this. I want to connect with families who are in similar situations and also show people who have no idea what it’s like to care for someone with a disability (or even a loved one who is sick) that it can be rewarding. Super fucking hard. Exhausting. Painful. Isolating. But, rewarding.
I’m going to get help for my sister - and others. My hope is that by sharing our story, I can bring awareness to the lack of services and help for the disabled.
This made me cry
STOP SCROLLING. THIS PERSON ISN’T ASKING FOR MONEY AND THIS POST WON’T MAKE YOU SAD.
This is a really uplifting and inspirational story of a family sticking by each other and making things work despite a whole lot of shit
They just want to find other people in the same position they are, for a sense of community and to feel like they aren’t alone.
I know out of all of you, some of you have followers who are living with and taking care of intellectually or emotionally disabled family members, and this lovely and unbreakable pair of sisters need to find them.
10 Useful Grammar Tips for Your Resume seen at AvidCareerist. For other job hunting advice etc… go to the link. I’m guilty of #1 on this blog because I’m lazy. For How to Answer the Top 35 Asked Interview Questions from The Undercover Recruiter and links to questions that are illegal to ask go here.
reblogging because grammar.