It’s just another success story in a medical saga that has gone on for many decades now, making gradual but definite progress – witness the marked increase in life expectancy over the past fifty years.
Once again this year, the UBC Alma Mater Society (AMS) is taking part in “Shinerama”, the campaign by post-secondary students across Canada to raise funds and awareness for CF research and treatment; and once again this year, TransLink and its family of companies are pleased to be a part of it.
Post-secondary students, knowing they’re at the age when a lot of CF sufferers die, have been involved in the fight for over 45 years. That’s why the UBC AMS organizes its annual Shinerama campaign. It’s truly a “clean and polished” concept: students hit the streets on the first weekend of the school year, shining shoes in return for contributions to the Canadian Cystic Fibrosis Foundation.
TransLink is supporting Shinerama in a number of ways. You’ve probably seen the ads on the large digital screens in SkyTrain stations on the Expo and Millennium Lines – the work of TransLink’s graphic artist, John Charron.
The BC Rapid Transit Company, the operator of SkyTrain, is making four stations available for the shoe-shining “blitz” on Saturday, Sept. 11. Bring your scuffed footwear – and your generous donations – between 11am and 4pm to one of the following stations:
- Granville
- Burrard
- Commercial-Broadway or
- Brentwood
Coast Mountain Bus Company will supply one of its buses for a special appearance during Orientation Week at UBC from 11am till 1pm on Tuesday, Sept. 7, where it will get its own “shine” from Shinerama volunteers outside the Student Union Building.
The connection between TransLink and CF is unavoidable: Cystic Fibrosis is a genetic disease, but it can be aggravated by environmental factors like poor air quality. As public transit becomes more efficient and effective and the public embrace TravelSmart thinking and find ways of getting around that don’t involve private autos, Greater Vancouver’s air quality is improved and maintained.
Since 2005, TransLink has aggressively increased service in a number of areas, all of which emphasize air quality. Our replacing and expanding the fleet of electric trolley buses is a commitment to that low-emission mode of transit that will last another quarter century – the anticipated service life of the new coaches.
The new diesel buses acquired over that time run on ultra low sulfur diesel fuel, with its sharply reduced greenhouse gas emissions, and are fitted with particulate traps, which screen out 90% of pollutants from the exhaust.
The opening of the SkyTrain Canada Line a year ago and the arrival of 48 new cars for the Expo/Millennium Lines have provided more incentive for people to choose transit over private autos. TransLink’s support of cycling infrastructure, both by co-funding municipal projects and taking on major work such as the Central Valley Greenway and the bike/pedestrian bridge that forms part of the Fraser River North Arm Bridge on the Canada Line, adds to that incentive and also helps promote active commuting.
TransLink’s AirCare program makes sure private automobiles do their part, too. Since its inception in 1992, hundreds of thousands of motor vehicles have been repaired after going through an AirCare test and, combined with improvements in automotive technology over that same time, has brought an improvement in air quality in the region, despite a steady increase in the number of motor vehicles.
Particularly important is the reduction of fine particulate matter (PM) from the atmosphere. Research has shown there is a strong link between the level of PM and human health effects. It is estimated that, without AirCare, the amount of vehicle emissions today – including PM – would be 29% higher than it currently is. That would make it harder for all of us to breathe – especially those with CF.
CF is a “blameless” disease: children get it through a genetic defect. One in 25 Canadians is a “carrier”, having that defective gene in their chromosomal structure; should two carriers become parents together, there’s a 1 in 4 chance a child they have will have CF.
CF literally leaves one breathless. A person with CF doesn’t have the inhibitor that most of us have, which prevents mucus from forming in the lungs. As that mucus builds and thickens, bacteria, which would normally be exhaled or coughed out, sticks around in the system, increasing the chance of disease. The mucus also clogs the ducts around the pancreas, which blocks enzymes from getting to the intestines to digest food.
Treatment includes pounding on the chest frequently to break up the mucus (when this writer was at UBC’s campus radio station in 1974, we ran a campaign to purchase percussors – devices that perform that “pounding” treatment), and a variety of drugs and inhalants. A CF patient also has to swallow an average of 20 enzyme pills a day with their meals in order to extract the nutrients from the food they eat.
We’ve only really known anything about CF since the 1930s, when people didn’t recognize a child had the disease until after he or she had died. But research has been making huge strides in identifying the cause and helping people with the disease lead increasingly better lives.
For example, in 1960, a child with CF rarely lived past the age of 4. In 1987, a 22-year-old Regina woman who made headlines with a trip to London for a double-lung transplant had already “beaten the odds” (sadly, she died not long after getting the transplant).
Today, the median age is 37 and up to half of all Canadians with CF are expected to live into their 40s and beyond. Most people with CF can now lead fairly normal lives, in terms of social relationships, physical activity and educational pursuits, although they still need a daily routine of rigorous physical therapy and regular visits to CF clinics. Efforts to improve quality of life and attack the genetic defect causing the disease have clearly been paying off, and research shows plenty of hope and promise.
So whether you’re cheering on the volunteers shining up our bus at UBC on Sept. 7 or getting your shoes shined on Sept. 11, please remember to give generously to the Canadian Cystic Fibrosis Foundation, so more people can breathe a lot easier!

It's the instructions for getting to the event on public transit. Whenever we have a major event in Vancouver -- Celebration of Light, major concerts or sports games -- we always send out a media advisory listing the various ways of getting there and back on bus, SkyTrain, or SeaBus. Are there additional trips? Does service run later? How do you get tickets? All of this is done while keeping in mind the fact that there are some people who aren't familiar with the public transit system.