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LOWE ROCHE Receives Exceptional Public Awareness Program Award

LOWE ROCHE, ALS Society of Canada’s new pro bono advertising agency, received the Exceptional Public Awareness Program Award in the media category in recognition of their exceptional effort to educate the public and increase awareness of ALS.

FOR IMMEDIATE RELEASE

PRLog (Press Release) - May 06, 2009 -
TORONTO, CANADA.  LOWE ROCHE, ALS Society of Canada’s new pro bono advertising agency,  received the Exceptional Public Awareness Program Award in the media category at an awards ceremony in Toronto on May 2, 2009. LOWE ROCHE created a Public Service Announcement (PSA) campaign in 2008 to raise public awareness of ALS.

The powerful PSA campaign consists of 30- and 60- second television spots in English and French and a series of three print advertisements. The campaign pulls no punches: the television spots, set to the children’s song “Head and Shoulders, Knees and Toes,” graphically documents the degeneration caused by this devastating disease. The print ads use simple, childish chalk drawings to illustrate the break-down in communication between the brain and the body of people living with ALS.

The spots have aired on local and national networks in Canada, on YouTube, where they have been viewed more than 36,000 times, and they have been posted in advertising blogs around the world. When the PSA campaign first appeared in November 2008, Jennifer Wells made this comment in her blog on globeandmail.com: “We don’t spend enough time, here in blog land, discussing the laudable pro bono work undertaken by the country’s advertising agencies… [LOWE ROCHE’s] 60-second spot is powerful, on-message, precisely right.”

The Exceptional Public Awareness Program Award recognizes exceptional programs that aim to educate the public and increase awareness of ALS. Activities in this category may include liaising with the media, coordinating public awareness displays and public speaking.

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About ALS:
ALS, also known as Lou Gehrig’s disease, is a rapidly progressive and fatal neuromuscular disease that causes the degeneration of nerve cells in the brain and spinal cord. ALS can affect men and women from any ethnic origin at any age. Approximately 2,500 to 3,000 Canadians are living with the disease. And 80 per cent of those affected will die within two to five years of diagnosis.

About the ALS Society of Canada:
The ALS Society of Canada, founded in 1977, is the only national voluntary health organization dedicated solely to the fight against ALS and support for those living with ALS. ALS Canada funds research towards a cure for ALS, supports the provincial ALS societies in the provision of quality care for those living with ALS, and provides information to build public awareness about the disease. The vision of the ALS Society of Canada is to find a cure for ALS.

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Contact Email:
***@als.ca Email Verified
Source:Bobbi Greenberg
Phone:416-497-2267 ext. 208
Fax:416-497-1256
Address:300-265 Yorkland Blvd.
Zip:M2J 1S5
City/Town:Toronto
State/Province:Ontario
Country:Canada
Industry:Non-profit, Health
Tags:, , , , ,
Last Updated:May 06, 2009
Shortcut:http://prlog.org/10231041
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