First night of show with hair and make-up \o/

First night of show with hair and make-up \o/

4 hours of pin curls and I’m orphan Annie #hardknocklife

4 hours of pin curls and I’m orphan Annie #hardknocklife

Someone was cold enough to warrant me giving up my hoodie for the greater good #Murcia #starspangledballerina

Someone was cold enough to warrant me giving up my hoodie for the greater good #Murcia #starspangledballerina

masterof-theworld:

Jamie Braddock
as stable as they come

unmarvel:

How Marvel Characters Eat Their Food [x]

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every single time i write sins not tragedies starts playing: haha, ohhhh this song. man oh i shouldnt sing it this time i havent heard it in so long. naahh not gonna do it. i dont even remember how it- OH, WELL IMAGINE, AS IM PACING THE PEWS IN A CHURCH CORRIDOR

nietzscheisdead:

six things every girl will ALWAYS have in her purse:

  1. another smaller purse
  2. an aging picture of ringo starr
  3. a six pack of heineken 
  4. the complete box set of every season of Deadliest Catch
  5. the hat you thought you lost at Disneyland when you were 5
  6. a tiny, infinitely dense marble that contains our own universe

slavocracy:

sorry white people but if you dont support mike brown & the people of fergusons’ protests in 2014 you probably wouldnt have supported abolition in the 1800s or civil rights movements in the 1960s & having the ability to recognize something as morally justified in hindsight something that has already been accepted by the mainstream as morally justified is nice for u but on all practical levels useless to everyone else 

castorochiaro:

Guardians of the Galaxy was such a fantastic movie!”

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"There were a lot of issues with GotG that should be addressed and Marvel should work on improving with future movies."

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madlori:

jmathieson-fic:

mumblingsage:

decodethefallenmoon:

molokoko:

amazing

“Just so everyone is aware, there is a bunch of misleading info being spread around re: ALS research - the “27%” figure is based on previous years’ annual funding; furthermore, the remainder goes to improving the quality of life of those suffering from ALS. Given that the annual funding is approximately 16M, that’s just over 4M spent on decreasing their suffering. It isn’t greed, it’s a lack of money.”Shut up already.

The ALS Association has a 4-star rating from Charity Watchdog. 
And the next time you start to complain about a charity either a) working on multiple fronts (because that’s what ALSA does—both seeking a cure and helping people suffering now) or b) daring to have administration expenses—let’s see how long you can last, much less tackle a cause, without printer paper and an internet connection. 

As someone who has watched a family member die from a neuro-degenerative disease; funding to develop better wheelchairs and bedsore creams is *just* as important as funding research to cure the disease itself…

A friend of mine posted an update from one of HER friends to FB earlier.  Her dad has ALS.  The ALS foundation came out to see if they could put in a ramp for his wheelchair, but they couldn’t afford it because of the kind of ramp he needed for the kind of house they had.
This week they called back and said hey, the thing is, we suddenly have a bunch of money, so we’re coming out to build that ramp.  And they did.  She posted pics.
So if you feel like bitching about the ice bucket challenge…reconsider.

madlori:

jmathieson-fic:

mumblingsage:

decodethefallenmoon:

molokoko:

amazing

Just so everyone is aware, there is a bunch of misleading info being spread around re: ALS research - the “27%” figure is based on previous years’ annual funding; furthermore, the remainder goes to improving the quality of life of those suffering from ALS. Given that the annual funding is approximately 16M, that’s just over 4M spent on decreasing their suffering. It isn’t greed, it’s a lack of money.”

Shut up already.

The ALS Association has a 4-star rating from Charity Watchdog. 

And the next time you start to complain about a charity either a) working on multiple fronts (because that’s what ALSA does—both seeking a cure and helping people suffering now) or b) daring to have administration expenses—let’s see how long you can last, much less tackle a cause, without printer paper and an internet connection. 

As someone who has watched a family member die from a neuro-degenerative disease; funding to develop better wheelchairs and bedsore creams is *just* as important as funding research to cure the disease itself…

A friend of mine posted an update from one of HER friends to FB earlier.  Her dad has ALS.  The ALS foundation came out to see if they could put in a ramp for his wheelchair, but they couldn’t afford it because of the kind of ramp he needed for the kind of house they had.

This week they called back and said hey, the thing is, we suddenly have a bunch of money, so we’re coming out to build that ramp.  And they did.  She posted pics.

So if you feel like bitching about the ice bucket challenge…reconsider.