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Geerlof Receives Sidney Valo Exceptional Fundraising Award

Calgary resident Hank Geerlof received the ALS Society of Canada Sidney Valo Exceptional Fundraising Award (Individual) in recognition of excellence in fundraising.

FOR IMMEDIATE RELEASE

PRLog (Press Release) - May 06, 2009 -
TORONTO, CANADA.  Calgary resident Hank Geerlof received the ALS Society of Canada Sidney Valo Exceptional Fundraising Award (Individual) at an awards ceremony in Toronto on May 2, 2009, in recognition of his volunteer contributions to the ALS community of Canada.

Single-handedly collecting more than $80,000 in three years for Betty’s Run for ALS, Geerlof has been tirelessly fundraising for the ALS Society of Alberta since his own diagnosis in 2003. He is an active member of the board of directors and led the society in the development of a five-year strategic plan. A participant in the steering committee of Elizabeth’s Concert of Hope in 2006, Geerlof helped to raise $140,000.

Recruiting family and friends to raise funds and awareness for the ALS community of Canada, Geerlof helped new volunteers become passionate about assisting the community. Despite facing his own challenges, Geerlof continues to dedicate his time and energy towards helping others with ALS.

“Over the last 5½ years, Hank has continuously given himself to the ALS Society of Alberta in many ways,” says Jane Rivest, client services co-ordinator at the ALS Society of Alberta. “Whenever and wherever he could help, Hank was always willing.”

The Sidney Valo Exceptional Fundraising Award recognizes excellence in fundraising programs implemented during 2008. In January 2009, this award was renamed to honour the work and commitment of Sidney Valo, member of the ALS Canada Board, who died on December 24, 2008.

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About ALS:
ALS, also known as Lou Gehrig’s disease, is a rapidly progressive and fatal neuromuscular disorder 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. Eighty 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/10231032
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