Sub Pop


News from 1/2007

FRI, JAN 19, 2007 at 8:47 AM

Loney, Dear - I Am John

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Emil Svanängen is the core of Loney, Dear. The first download from Loney, Dear’s new album Loney, Noir is called “I Am John”. ConfusING? Do you yearn to know who this John person is? Listen to the song and find out… maybe.


Posted by Chris Jacobs

FRI, JAN 19, 2007 at 11:42 AM

J. ROBBINS, HIS WIFE JANET, THEIR SON CALLUM

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Though we haven’t worked with J. Robbins, many of us here have been/are fans of his work as a musician and producer. When the news below reached us, we felt compelled to pass it along to all of you. Please take a moment to read through it, and do what you can.

Thanks.

(Lifted straight from the DeSoto Records website…)

On January 27, 2006, our great friends and Channels members J. Robbins and Janet Morgan welcomed their first child, a son named Callum. He was 8-odd pounds and 20-odd inches of wriggling, squirming, screaming joy, and the apple of his parents’ eye.

As Cal grew, though, his parents began to notice that the expected developmental milestones – biting his toes, squeezing Janet’s finger, even rolling over and sitting up unsupported – weren’t happening. As a parent, you never want to think that something is wrong with your child. You bury your doubts and convince yourself that your baby is just different, that he’s got his own way of doing things, that he’s just “mellow.” You’ve got diapers to change, bottles to warm, baths to give. Life has to go on.

Sometime around Cal’s 8-month birthday in September, J. and Janet took him to his pediatrician for his regular appointment. They knew from the doctor’s grave tone that something was terribly wrong. Any parent — any human — reading this can understand the shock, horror, and pain that J. and Janet felt when they learned through subsequent visits with specialists that Cal was born with a genetic motor neuron disease called Type 1 SMA, or Spinal Muscular Atrophy.

The facts are brutal: SMA kills kids. The disease affects the brain’s ability to communicate with the voluntary muscles that are used for activities such as crawling, walking, head and neck control, breathing, and swallowing. Type 1 SMA is usually fatal; most Type 1 babies will die before their second birthday. Those infants who survive into childhood are in for a long road of occupational therapy, wheelchairs, and assistive devices. Despite years of work on its treatment and “ongoing promising research,” it has no cure.

J., Janet, and Cal live every day with this disease hanging over their heads, and the path before them is extremely expensive and consuming of their former “normal lives.” Cal will never be able to walk. Once he is old enough to require a wheelchair, he will be wheelchair-bound for life, which likely also means at some point he’ll need surgery to correct for scoliosis.

It is an understatement to call this a heartbreaking situation. It also stands to be an unbelievably expensive one, especially for a household where the only wage-earner is a self-employed indie recording engineer. It remains unclear just how helpful J.’s single-payer insurance will be.

Allopathic (“conventional”) doctors, while energetically engaged in research into this condition, can offer no cure for Callum. There may be some hope — even if only for a better quality of life — in alternative routes and therapies. These, of course, are not covered by health insurance.

We at DeSoto feel that we owe it to J., Janet, and Callum to explore any and every avenue that might help their little boy. Pursuing alternative treatments will very plausibly bankrupt them.

Our hope is that people whose lives J., Janet, and Cal have touched – with their music, their friendship, their work in the independent music community – can help. Every dollar you give will provide Cal support to pursue treatment for this terrible disease. Perhaps more important, it will provide J., Janet, and Cal some of the hope they need to play out this horribly unfair hand life has dealt them.

Best,
—Kim, Bill, and Nick

The info on how you can donate is here.


Posted by Chris Jacobs

FRI, JAN 19, 2007 at 10:58 AM

An announcement from Dead Moon

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After 20 yrs, Dead Moon is retiring. It has been a journey we will always treasure and feel that a worldwide family has emerged in its place. Dead Moon became much bigger than the band itself, it became a DIY underground hopeful for a lot of people. The candle is still burning!
—Fred Cole

Dead Moon’s site


Posted by Chris Jacobs

FRI, JAN 19, 2007 at 11:56 AM

The Shins are going on tour!

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The first cluster of U.S. dates are now confirmed, and we’re announcing it RIGHT THIS SECOND!!! CAN YOU BELIEVE IT!! Get your tickets fast-like, ’cause these suckers will likely sell out. Here are all the confirmed dates!


Posted by Chris Jacobs

FRI, JAN 19, 2007 at 10:30 AM

LOW AND THE MAASAI SCHOOL PROJECT

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Our friends in the band Low have been involved in a project to help increase adult literacy in Kenya. They’ve used money from Christmas shows this year and in 2005 to help fund the building of a school in Namuncha, Kenya.

You can read a bit about all this from Low’s Alan Sparhawk, on Low’s own website.

There’s also an article about all this in the Minneapolis Star Tribune.

And then, you can read a whole lot more about the Maasai School Project on their website, and see photos of Alan’s trip to Kenya this past August.
Because often things that should go without saying don’t: you could do worse things than donate to this project yourself.


Posted by Chris Jacobs

THU, JAN 18, 2007 at 9:58 AM

Happy New Year, pals!

We’re back from holiday and ready to kick some online shopping ass in 2007.

All orders placed betwixt Dec 22 and Jan 2 have just been shipped out this week, excluding the new Shins album, of course.


Posted by Chris Jacobs