I remember all the Doctor Who fanfics I used to read where Rose often got badly stereotyped as a damsel in distress whom the Doctor had to swoop in and save and smooch but the way I remember Doctor Who 90% of their relationship was the Doctor just setting Rose loose on people who had done something to offend them and sitting back giggling in the corner as she shouted
setting Rose loose
Snape, Snape, Severus Snape, DUMBLEDORE
BUT THAT IS NOT HOW IT GOES
ROOn, ROOn, ROOn Weeeeasley
“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.
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.
This is so so so important. ALSA doesn’t just research for a cure, they help the everyday lives of people living with ALS. I get really mad everytime I see people on facebook thinking that the people who run ALSA are getting a huge raise and that just isn’t true okay????