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  • Claire b (@Clairesb2012) tweeted at 3:13 PM on Sun, Dec 02, 2012: To submit a design, or not to submit, that is the question… (https://twitter.com/Clairesb2012/status/275256459040784385) Get the official Twitter app at https://twitter.com/download

    • 5 months ago
  • Claire b (@Clairesb2012) tweeted at 0:02 AM on Wed, Nov 28, 2012: sons of an illustrious father…seriously cool unique sound…love it! (https://twitter.com/Clairesb2012/status/273577570941947904) Get the official Twitter app at https://twitter.com/download

    • 5 months ago
  • Good philosophy, make it a better one x

    Good philosophy, make it a better one x

    (via hitrecordjoe)

    Source: barackobama
    • 7 months ago
    • 8938 notes
  • loopermovie:

Ladies and gents, it’s time to meet our secret weapon: Pierce Gagnon.

Excellent actor at such a young age! Cute but seriously scary…nice work!!!

    loopermovie:

    Ladies and gents, it’s time to meet our secret weapon: Pierce Gagnon.

    Excellent actor at such a young age! Cute but seriously scary…nice work!!!

    Source: loopermovie
    • 7 months ago
    • 572 notes
  • Claire b (@Clairesb2012) tweeted at 9:32 PM on Fri, Sep 28, 2012:
    One word to describe looper…awesome!!! Mr Johnson is an absolute genius! And stunning performances all round x
    (https://twitter.com/Clairesb2012/status/251781330617106432)

    Get the official Twitter app at https://twitter.com/download

    • 7 months ago
  • Claire b (@Clairesb2012) tweeted at 7:34 AM on Thu, Sep 27, 2012:
    According to Douglas Adams the answer to life, the universe and everything is 42…so what on earth was the question???
    (https://twitter.com/Clairesb2012/status/251208131403718656)

    Get the official Twitter app at https://twitter.com/download

    • 8 months ago
  • hitrecordjoe:

So happy to keep with my little tradition of making one of the SNL portraits my internet avatar.
Thanks to SNL’s wonderful staff photographer, Mary Ellen Matthews, for hitting the button. :oD

Very debonair, like her work x

    hitrecordjoe:

    So happy to keep with my little tradition of making one of the SNL portraits my internet avatar.

    Thanks to SNL’s wonderful staff photographer, Mary Ellen Matthews, for hitting the button. :oD

    Very debonair, like her work x

    Source: hitrecordjoe
    • 8 months ago
    • 5442 notes
  • Holy fuck I love this! Hilarious  :-)

    Holy fuck I love this! Hilarious :-)

    Source: loopermovie
    • 8 months ago
    • 45 notes
  • superamit:

One year ago today my doctor called me in the afternoon.
I was in bed. He cleared his throat a couple times and then he told me the reason I’d been feeling weak, seeing weird blindingly bright spots in my vision, and had a fever that wouldn’t go away was because my blood was full of ineffective, malformed white blood cells.
I had AML leukemia. If I did nothing, I’d die in a few weeks. 
A few hours later, I had a flight to the East Coast booked for early the next morning. I spent the night in a San Francisco hospital getting blood transfusions and antibiotics to allow me to fly.
I landed in NYC, my parents picked me up, and we drove to Yale’s Smilow Cancer Hospital. When they started pumping cell-killing poison into my bloodstream, the hospital became my home and my prison for the next few months.
I cried. I felt sorry for myself. I didn’t believe it was true.
Friends banded together and started drives across the country, then across the globe. I did interview after interview. Newspapers, TV, and radio helped spread the word. Facebook, twitter, and tumblr got people to drives. I couldn’t leave the hospital, and sometimes I was throwing up too much or too weak to talk. We kept going.
We organized online, and my prison became our stem cell drive campaign headquarters.
Friends donated time, money, connections. Strangers sent mail, hundreds of photos, and organized drives. Celebrities made videos. Tens of thousands registered to be stem cell donors. (Matches for others in need continue to come out of those drives.)
The nurses and doctors continued to pump poison into my blood, eliminating cancerous cells and healthy cells alike. They hoped to hold the leukemia at bay until a donor could be found.
A few months later, we found a donor! Friends and strangers had banded together to save my life.
I had my transplant in late January. And then began the year-long recovery process I’m currently in:
15-20 pills a day, on-and-off steroids to combat Graft vs Host Disease, nausea, weakness, muscle atrophy, scopes down my throat, probes up my nose until they hit my throat. Weekly, then bi-monthly blood tests, immunosuppressants - which keep my immune system from attacking my organs, but also make me susceptible to disease. Needles, needles, needles, so many needles, fevers, infections, severe mucositis, so much pain they gave me a button to press to give myself morphine whenever I wanted, anti-nausea drugs that resulted in weeks of lost memories, blood clots, followed by months of blood thinners, teeth issues, corneal damage, a slate of other issues a little too graphic to write about, crazy painful out-of-nowhere hand and leg cramps…
…all bumps along the road.
My counts are up. There’s no sign of recurrence yet. If I’m lucky, there never will be. I feel more normal with each passing week.
I was able to leave the hospital, and then able to leave my parents’ home.
I got to spend the summer in NYC, reconnecting with old friends, and returning to work at Photojojo part-time. I just saw my brother get married, saw a live volcano in Hawaii, saw the sun set above the clouds and the clearest night sky in the world. I visited Portland for the first time, and spent a week in SF working and seeing friends. Now we’re planning a road trip to move back West. We leave in a few weeks… on motorcycles.
A year ago I was on a plane from SF to CT because I was dying.
Today I’m on a plane from SF to CT, and I feel more alive than I have in a very long time.
Photo @ Twin Peaks last week in SF.(See pics of our adventures by following @superamit on Instagram or follow this Tumblr!)

I think that you are incredibly brave, and the fact you keep going with hope is so inspiring. I know how it feels to feel like you’re number has been called too early and I think the fact you are fighting makes you a super hero. Keep on going! X

    superamit:

    One year ago today my doctor called me in the afternoon.

    I was in bed. He cleared his throat a couple times and then he told me the reason I’d been feeling weak, seeing weird blindingly bright spots in my vision, and had a fever that wouldn’t go away was because my blood was full of ineffective, malformed white blood cells.

    I had AML leukemia. If I did nothing, I’d die in a few weeks.

    A few hours later, I had a flight to the East Coast booked for early the next morning. I spent the night in a San Francisco hospital getting blood transfusions and antibiotics to allow me to fly.

    I landed in NYC, my parents picked me up, and we drove to Yale’s Smilow Cancer Hospital. When they started pumping cell-killing poison into my bloodstream, the hospital became my home and my prison for the next few months.

    I cried. I felt sorry for myself. I didn’t believe it was true.

    Friends banded together and started drives across the country, then across the globe. I did interview after interview. Newspapers, TV, and radio helped spread the word. Facebook, twitter, and tumblr got people to drives. I couldn’t leave the hospital, and sometimes I was throwing up too much or too weak to talk. We kept going.

    We organized online, and my prison became our stem cell drive campaign headquarters.

    Friends donated time, money, connections. Strangers sent mail, hundreds of photos, and organized drives. Celebrities made videos. Tens of thousands registered to be stem cell donors. (Matches for others in need continue to come out of those drives.)

    The nurses and doctors continued to pump poison into my blood, eliminating cancerous cells and healthy cells alike. They hoped to hold the leukemia at bay until a donor could be found.

    A few months later, we found a donor! Friends and strangers had banded together to save my life.

    I had my transplant in late January. And then began the year-long recovery process I’m currently in:

    15-20 pills a day, on-and-off steroids to combat Graft vs Host Disease, nausea, weakness, muscle atrophy, scopes down my throat, probes up my nose until they hit my throat. Weekly, then bi-monthly blood tests, immunosuppressants - which keep my immune system from attacking my organs, but also make me susceptible to disease. Needles, needles, needles, so many needles, fevers, infections, severe mucositis, so much pain they gave me a button to press to give myself morphine whenever I wanted, anti-nausea drugs that resulted in weeks of lost memories, blood clots, followed by months of blood thinners, teeth issues, corneal damage, a slate of other issues a little too graphic to write about, crazy painful out-of-nowhere hand and leg cramps…

    …all bumps along the road.

    My counts are up. There’s no sign of recurrence yet. If I’m lucky, there never will be. I feel more normal with each passing week.

    I was able to leave the hospital, and then able to leave my parents’ home.

    I got to spend the summer in NYC, reconnecting with old friends, and returning to work at Photojojo part-time. I just saw my brother get married, saw a live volcano in Hawaii, saw the sun set above the clouds and the clearest night sky in the world. I visited Portland for the first time, and spent a week in SF working and seeing friends. Now we’re planning a road trip to move back West. We leave in a few weeks… on motorcycles.

    A year ago I was on a plane from SF to CT because I was dying.

    Today I’m on a plane from SF to CT, and I feel more alive than I have in a very long time.

    Photo @ Twin Peaks last week in SF.
    (See pics of our adventures by following @superamit on Instagram or follow this Tumblr!)

    I think that you are incredibly brave, and the fact you keep going with hope is so inspiring. I know how it feels to feel like you’re number has been called too early and I think the fact you are fighting makes you a super hero. Keep on going! X

    Source: superamit
    • 8 months ago
    • 39448 notes
  • The road most travelled…

    They say the road to hell is paved with good intentions. But what of the road back? I believe that road is paved with hindsight and humility, and we’ve all travelled that one at some point in our lives. What do you guys think?

    • 8 months ago
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