write-it-in-the-sky:

    nomadic-queer-punk:

    hiddles-is-life:

    comfortspringstation:

    Kitten rejected by mother and raised by golden retriever

    So cute it make me wanna cry.

    too damn precious. my heart will explode.

    🐶🐱

    (via amanogawatea)

  1. (Source: princess-tanzanite, via bilbochan)

    listoflifehacks:

    If you like this list of life hacks, follow ListOfLifeHacks for more like it!

    (via harzilla)

    hastyslam:

    Ashe Cosplay - League of Legends

    Source

    (via xx-josuke4ballz-6969-xx)

  2. lilacck:

    crystalmoon

    (via m-i-l-k--y)

  3. shingekinokyojinheaven:

    on the internet:

    image

    in real life:

    image

    (via m-i-l-k--y)

  4. thepathtowonderland:

    wiggitawiggitawack:

    seaworlcl:

    what if bees sang songs when they flew by your ears

    [tiny bee whisper/sings] ah ah ah ah stayin alive

    im a boss ass bitch bitch bitch bitch bitch bitch bitch 

    (via m-i-l-k--y)

  5. toasty-coconut:

    edamarie:

    free him

    free him

    (Source: digiorno.com, via tempestpaige)

  6. lmaoalien:

    awkward in person, funny and social on the internet

    (via m-i-l-k--y)

  7. halfbakedpoet:

    And here we see a majestic wild mop without a handle frolicking on a beach…

    (Source: photosynthesis206, via harzilla)

  8. My Parents are Dead and My Sister is Disabled

    congalineofdurin:

    cockismybusiness:

    team—wolverine:

    therealbarbielifts:

    eisforedna:

    On May 28th, my sister, Edna, turned 31.

    image 

    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. 

    image

    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. 

    image

    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.) 

    image

    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.

    image

    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. 

    image

    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. 

    image

    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: 

    image

    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. 

    image

    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. 

    image

    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. 

    image

    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.

    image

    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: 

    image

    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.

    image

    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. 

    Thank you, 

    Jeanie 

    Facebook:  facebook.com/eisforedna

    Twitter: @EisforEdna 

    This made me cry

    SIGNAL BOOST

    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.

    SIGNAL BOOOOOOOOOST

    (Source: , via squidkneee)

  9. unclewhisky:

    anymousse:

    And now, a deep moment from Dr Heinz Doofenshmirtz.

    A-ha! Explanation time!

    Those skulls you’re always seeing in westerns are a trope that comes from the massive buffalo die-offs from the late 19th century. Basically what happened was, the American government started offering bounties on buffalo hides, meat, and other products, and gave those bounties out like candy. Professional hunters, and just regular bored people with guns (of which there were many in the 1890s western frontier), swept into western Texas and surrounding areas, and proceeded to more-or-less exterminate the American buffalo population. The reasoning for this was not because the American people had discovered the tasty, tasty miracle of buffalo burgers, but because the U.S. Army was actively waging a campaign of economic terrorism against the southern plains tribes of American Indians, primarily the hostile Comanche and Apache tribes, who relied on the buffalo for most of their material goods.

    While they’re at it, of course, the hunters and armed hooligans would bring the hides and bones in to trading posts, where they were often sold back to the Indians at outrageously high prices. Because of the extermination program, though, this was pretty much the only way the Indians could get the goods they needed, so they had no choice but to pay the American traders and hunters.

    The skulls, the hunters figured, had little resale value except as a cultural/religious artifact, and since the American government had a vested interest in destroying native religious practices (since that was a main source of Indian resistance, such as the Ghost Dance ritual), hunteres were discouraged from selling the skulls. The fact that very few tribes actually used the skulls in their religious practices seems to have been overlooked because then, as now, most Americans know next to nothing about the people who lived in this country before we did.

    And that is why the image of a sun-bleached buffalo (not cow) skull, sitting alone in the desert with no body to accompany it, is such an oft-used symbol of the American west. It is, ultimately, a tragic symbol, because the story of the American west is, by and large, a tragedy. The fact that few enough people know the story that it can be the butt of a joke in a kids’ cartoon makes it no less tragic.

    (Source: jaguarslair, via xx-josuke4ballz-6969-xx)



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