Cystic Fibrosis: Too White to Cure
By Joanne Laucius
David Duke Comments
The Carleton University Students’ Association has voted to drop a cystic fibrosis charity as the beneficiary of its annual Shinearama fundraiser, supporting a motion that argued the disease is not “inclusive” enough.
Cystic fibrosis “has been recently revealed to only affect white people, and primarily men” said the motion read Monday night to student councillors, who voted almost unanimously in favour of it.
Every year near the beginning of fall classes, during university orientation for new arrivals, students fan out across the city and seek donations from passersby. According to the motion, “all orientees and volunteers should feel like their fundraising efforts will serve their diverse communities.”
Nick Bergamini, a third-year journalism student on the student council, said he was the only elected councillor present to vote against the motion. The decision is an example of campus political correctness gone too far, he said.
“They’re not doctors. They’re playing politics with this,” said Mr. Bergamini. “I think they see this, in their own twisted way, as a win for diversity. I see it as a loss for people with cystic fibrosis.”
The Shinearama fundraiser is carried out by students at about 65 colleges and universities across Canada. It has raised money for the Canadian Cystic Fibrosis Foundation for almost 50 years and Carleton has been participating for at least 25.
During orientation week this year, Carleton students, who have raised about $1-million over the years, raised about $20,000, said foundation chief executive Cathleen Morrison, who was surprised and dismayed by the student association decision.
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