Arguments & objections. Make a connection. Open your eyelid, scan the horizon. Waking to dream with the brave and defiant.


Video

Jan 24, 2012
@ 10:04 pm
Permalink

People Say by Portugal. The Man


Photo

Jan 24, 2012
@ 8:32 pm
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(Source: mystandards, via le-nickasaur)


Photo

Jan 18, 2012
@ 6:16 pm
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publicradiointernational:

soupsoup:

strle:

superamit:

Many of you have asked, so here’s what’s going on with me.
WHAT HAPPENED BEFORE
8/1979: Born. Grew up in CT, built a killer eraser collection, fell in love with computers.
Left college to start a company. Fell hard. Fled to India for 3 months.
Started 2nd company. Learned to be an adult. Fell in love with NYC.
Moved to SF, discovered burritos & some of my fave people on Earth.
9/2011: Got diagnosed with Leukemia!
Cried. Went through 3 cycles of chemo. Hurt. Thought hard about what I want out of life. Grew up a second time.
TODAY
… After over 100 drives organized by friends, family, and strangers, celebrity call-outs, a bazillion reblogs (7000+!), tweets, and Facebook posts, press, fundraising and international drives organized by tireless friends, and a couple painful false starts, I’ve got a 10/10 matched donor!
You all literally helped save my life. (And the lives of many others.)
WHAT HAPPENS NEXT
Tomorrow, I’ll be admitted to Dana Farber in Boston for 4-5 weeks.
First I’ll get a second Hickman line to allow direct access to my heart (for meds and for nutrients if I’m not able to eat). Over the next week, the docs blast my body with a stiff chemo cocktail to try and eradicate all traces of cancer cells. In the process, the immune system I was born with, and my body’s ability to make blood, are destroyed.
Next Friday, I get my donor’s stem cells by IV. I start on immunosuppressants to prevent my body from rejecting them (I’ll be on them for 12-18 months). For these weeks I’ve no immune system, so I’m severely vulnerable to viruses and bacteria. My hospital room and hallway become my world.
Meanwhile, the stem cells make their way to my bone marrow and, with some luck, start producing platelets, red blood cells, and white blood cells. At this point, my blood type changes to the blood type of my donor. And my blood will now have my donor’s DNA, not my own.
This is science fiction stuff. I can hardly believe it’s even possible, and there’s lots of chances for things to go wrong. It’s frightening.
AFTER THE TRANSPLANT
Recovery to a new state of “normal” takes about a year, but there’s a few storm clouds hovering:
My immune system is new, like a baby’s. I’m prone to getting sick.
Just as with any organ transplant, there’s a chance of rejection. Except in this case, it’s my blood that’s the foreign body, and it touches every organ. They call it graft-vs-host-disease and it can cause health issues and organ complications for the rest of my life.
Successful transplant or not, Leukemia can relapse. Stubborn mofo.
Overall, 75% of AML transplant patients survive year one, 50% make it through year five. My odds are a little better since I’m young.
THE GREAT NEWS
I’ve got a long road ahead. But I’ve got a donor & amazing family & friends. A few months ago I didn’t have many options. Today I have a plan.
I am alive. I start tomorrow. Wish me luck!
Thank you.

<3

I have tears in my eyes. Deliriously happy for Amit, now go kick cancer’s ass.
This is great news. Amit was on our show, The Takeaway, on December 28 where he talked about getting close to finding a potential match. He also said about 10,000 people registered to be bone marrow donors thanks to the efforts of his friends.

publicradiointernational:

soupsoup:

strle:

superamit:

Many of you have asked, so here’s what’s going on with me.

WHAT HAPPENED BEFORE

  • 8/1979: Born. Grew up in CT, built a killer eraser collection, fell in love with computers.
  • Left college to start a company. Fell hard. Fled to India for 3 months.
  • Started 2nd company. Learned to be an adult. Fell in love with NYC.
  • Moved to SF, discovered burritos & some of my fave people on Earth.
  • 9/2011: Got diagnosed with Leukemia!
  • Cried. Went through 3 cycles of chemo. Hurt. Thought hard about what I want out of life. Grew up a second time.

TODAY

… After over 100 drives organized by friends, family, and strangers, celebrity call-outs, a bazillion reblogs (7000+!), tweets, and Facebook posts, press, fundraising and international drives organized by tireless friends, and a couple painful false starts, I’ve got a 10/10 matched donor!

You all literally helped save my life. (And the lives of many others.)

WHAT HAPPENS NEXT

Tomorrow, I’ll be admitted to Dana Farber in Boston for 4-5 weeks.

First I’ll get a second Hickman line to allow direct access to my heart (for meds and for nutrients if I’m not able to eat). Over the next week, the docs blast my body with a stiff chemo cocktail to try and eradicate all traces of cancer cells. In the process, the immune system I was born with, and my body’s ability to make blood, are destroyed.

Next Friday, I get my donor’s stem cells by IV. I start on immunosuppressants to prevent my body from rejecting them (I’ll be on them for 12-18 months). For these weeks I’ve no immune system, so I’m severely vulnerable to viruses and bacteria. My hospital room and hallway become my world.

Meanwhile, the stem cells make their way to my bone marrow and, with some luck, start producing platelets, red blood cells, and white blood cells. At this point, my blood type changes to the blood type of my donor. And my blood will now have my donor’s DNA, not my own.

This is science fiction stuff. I can hardly believe it’s even possible, and there’s lots of chances for things to go wrong. It’s frightening.

AFTER THE TRANSPLANT

Recovery to a new state of “normal” takes about a year, but there’s a few storm clouds hovering:

  • My immune system is new, like a baby’s. I’m prone to getting sick.
  • Just as with any organ transplant, there’s a chance of rejection. Except in this case, it’s my blood that’s the foreign body, and it touches every organ. They call it graft-vs-host-disease and it can cause health issues and organ complications for the rest of my life.
  • Successful transplant or not, Leukemia can relapse. Stubborn mofo.

Overall, 75% of AML transplant patients survive year one, 50% make it through year five. My odds are a little better since I’m young.

THE GREAT NEWS

I’ve got a long road ahead. But I’ve got a donor & amazing family & friends. A few months ago I didn’t have many options. Today I have a plan.

I am alive. I start tomorrow. Wish me luck!

Thank you.

<3

I have tears in my eyes. Deliriously happy for Amit, now go kick cancer’s ass.

This is great news. Amit was on our show, The Takeaway, on December 28 where he talked about getting close to finding a potential match. He also said about 10,000 people registered to be bone marrow donors thanks to the efforts of his friends.

(via discoverynews)


Photo

Jan 12, 2012
@ 7:40 pm
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Photo

Jan 8, 2012
@ 4:46 pm
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Drifters by Esao Andrews

Drifters by Esao Andrews


Photo

Dec 28, 2011
@ 11:11 pm
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marcomazzoni:

“Ocean of Noise” 2011, colored pencils on paper, cm 35x35
for “Lush Life 3”, Roq la Rue Gallery, Seattle (December 9th)

marcomazzoni:

“Ocean of Noise” 2011, colored pencils on paper, cm 35x35

for “Lush Life 3”, Roq la Rue Gallery, Seattle (December 9th)


Photo

Dec 27, 2011
@ 9:55 pm
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(Source: gone-so-young, via fuckyeah1990s)


Photo

Dec 16, 2011
@ 12:30 am
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(via le-nickasaur)


Photo

Dec 1, 2011
@ 10:50 pm
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fuckyeahjohnbaldwingourley:

from Twitter

fuckyeahjohnbaldwingourley:

from Twitter


Quote

Nov 27, 2011
@ 4:40 am
Permalink

I think that if I ever have kids and they are upset, I won’t tell them that people are starving in China or anything like that, because it wouldn’t change the fact that they were upset. And even if somebody else has it worse, that doesn’t change the fact that you have what you have.

— Stephen Chbosky, The Perks of Being a Wallflower (via larmoyante)


Text

Nov 27, 2011
@ 3:50 am
Permalink

onnothingandeverything:

There are times
when I’d like
to take you quietly aside,
so it’s just us
(and us alone)
pull you close,
take your hands in mine,
stare deep into your eyes
and earnestly ask,










“WHAT THE FUCK…?!”


Photo

Nov 23, 2011
@ 3:50 am
Permalink

Colin Frangicetto Art

Colin Frangicetto Art


Quote

Nov 20, 2011
@ 11:10 am
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Because paper has more patience than people.

— Anne Frank (via pavorst)

(via fuckyeahbookarts)


Quote

Nov 17, 2011
@ 8:48 pm
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What is important is what cannot be said, the white space between the words.

— Max Frisch


Photo

Nov 17, 2011
@ 8:33 pm
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allofyourfriendsaregone:

ecard at its best. 

allofyourfriendsaregone:

ecard at its best.