CF Foundation Develops Congressional Cystic Fibrosis Caucus in the USA, writes Cystic Fibrosis Foundation staffer Kathryn White in a moment of candor. (You can’t find this document directly on the internet anymore, but if you search for the headline on Google, then select the option “Vie...

Biotech, people, startups Luke Timmerman wrote: It’s cold outside, so I was a little bummed there was no actual fire at an event last night billed as a “fireside chat.” This get-together actually took some time to warm up (pun intended). But once it got rolling, three of the most e...

Ken wrote about the CUSA Shinerama scandal, like some other people I know.  He ends his entry with some information on how to contact Brittany Smyth, CUSA President, in particular how to send a message to her cell phone.  He didn’t do anything stalkerish to find this piece of information out...

I must admit that, like others, I was stunned when I learned that the Carleton University Students’ Association (CUSA) decided to stop supporting the Canadian Cystic Fibrosis Foundation through its Shinerama campaign during the frosh week activities because it “has been recently revealed...

... Donate it to the Canadian Cystic Fibrosis Foundation instead.  In fact, if you have a shred of decency, you won't give money to Carleton. Why? Well, it seems that the Carleton University Student Association doesn't believe that Cystic Fibrosis is worthy of support from their Shinerama campaign....

I can only sit and marvel at this latest stupidity. Cystic Fibrosis is a genetic disease that is the most common genetic illness in white people. Apparently that's racist. One would laugh, if one didn't want to cry. Even by the loopy standards of students governments, this has got to be a new low. H...