I just added a new way to support the show: Patreon. Think crowd-funding for artists. Become a patron starting as low as $1. Did I mention rewards? Yes, rewards will be based on the size of your patronage. And this is just the beginning. I’m planning for more rewards over time.
Of course TFTTF is free and will stay free. I’m very humbled by your awesome contributions, but they are not mandatory to be a listener of TFTTF.
Chris will briefly talk about the new iPhone 6 and how that relates to photography. He’ll also try to find the elusive value of art and let’s see if we can help brad to stylize his photos through post production.
You take a sunset picture. Oh no, not again. HDR? Seen it all. Or maybe a color key where a red rose sits lonely in a sea of black-and-white? Clichés are everywhere in photography. Chris explores how bad it really is if you choose to shoot a cliché picture.
A word from Chris: TFTTF needs your help. It is hard for me to ask for money, which is why I don’t do it often, but in a episode like this one that doesn’t have a sponsor paying for the servers (there are three of them), for the production time (it takes at least three hours to make one single episode) and for all the rest of the invisible but all important infrastructure, your support is crucial to help keep the Top Floor lights on.
The Ice Bucket Challenge is taking the world in storm. And to those who say “enough already”, I respond: if you don’t want to see it, ignore it.
Here’s what this is about: Amyotrophic Lateral Sclerosis, also known as ALS. It’s a devastating disease of the nervous system and simply said: it kills in a slow and horrible way. Patients slowly lose control over their muscles. ALL their muscles. One of the more famous people with ALS is Stephen Hawking.
ALS is not fun. ALS is dead serious. And the ice bucket challenge isn’t making light of it. The challenge is a wonderful way to raise awareness, and it’s necessary because most people don’t even know what ALS is. It’s is a rare disease of the nervous system (approx. 30,000 US Americans have it) and as a result of that, the pharmaceutical industry has no incentive of making any serious investments into finding a cure.
Which is why everybody should chip in for ALS and all the other rare neurological diseases. A good place to do so is the ALS Assocication at www.alsa.org.