Zugspitze IV
By: Christopher Getschmann

Zugspitze IV

By: Christopher Getschmann

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.

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.

nattles:

The pie booklet is now an iPhone app!

nattles:

The pie booklet is now an iPhone app!

By: Sunny.em

By: Sunny.em

danbusta:

Here is a film outtake from my Spring 12 shoot with Raven Denim. I shot this on one of my favorite cameras, the Nikon L35AF. This mass produced camera was the first autofocus point and shoot ever made. It was such a blast working that day back in August. We had a expensive location, three models, two amazing assistants, makeup, stylists the whole nine yards. It was the kind of shoot that photographers dream about. Especially shooting the great Melinda Rader, seen here. I look forward to our fall shoot coming up on my birthday Jan 15th, is there a better way to spend you birthday? I don’t think so. The rollerskating party will just have to be postponed. 

danbusta:

Here is a film outtake from my Spring 12 shoot with Raven Denim. I shot this on one of my favorite cameras, the Nikon L35AF. This mass produced camera was the first autofocus point and shoot ever made. It was such a blast working that day back in August. We had a expensive location, three models, two amazing assistants, makeup, stylists the whole nine yards. It was the kind of shoot that photographers dream about. Especially shooting the great Melinda Rader, seen here. I look forward to our fall shoot coming up on my birthday Jan 15th, is there a better way to spend you birthday? I don’t think so. The rollerskating party will just have to be postponed. 

Charlie Chaplin - The Great Dictator (set to Hans Zimmer’ Time)

Bob Ross + Squirrel

Phoenix Park on a Sunday, Dublin
Artist: Emily Hoefer
Year: 1966
Materials/Techniques: Dye Transfer Print

Phoenix Park on a Sunday, Dublin

Artist: Emily Hoefer

Year: 1966

Materials/Techniques: Dye Transfer Print

ryanschude:

this is a plastic seamless from when me and Dan went plexiglass shopping in the valley for our lightbox collabo.
©Ryan Schude

ryanschude:

this is a plastic seamless from when me and Dan went plexiglass shopping in the valley for our lightbox collabo.

©Ryan Schude

msg:

My friend and colleague Amit Gupta is fighting off leukemia and the twittersphere is lighting up with expressions of support.

But the support he really needs is for you to get a Q-tip, stick it in your cheek and mail it back. The process is free and you can sign up right here.

The extraordinary thing about marketing is that a million people might see something or hear something or be sold something and only a thousand will actually take action. Even if it’s free.

When you look at the long odds on marrow donation, it feels like a bit of a sweepstakes, but backwards. It’s easy to fix if we just get everyone (regardless of ethnicity) to register.

How about if we gamify it? Here’s the deal: if you are a match for Amit and the marrow donation happens, I’ll profile you or the project of your choice on the blog and send you a check for $10,000 for you or the charity of your choice. Winner take all, no purchase necessary, void where prohibited… (Even if you don’t win, if you swab we all win).

If I can be so bold as to suggest a hashtag: #IswabbedforAmit

====

I dont have the same following as Seth Godin but I will definitely match his offer. 

 if you are a match for Amit and the marrow donation happens, I’ll profile you or the project of your choice on the blog and send you a check for $10,000 for you or the charity of your choice. Winner take all, no purchase necessary, void where prohibited…