CA
Canadian Cancer Society - PEI
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À propos de l'organisation
The Canadian Cancer Society is a national, community-based organization of volunteers whose mission is the eradication of cancer and the enhancement of the quality of life of people living with cancer.
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- Site Web
- http://www.cancer.ca
- Lieu
-
5826 South St
Halifax, Nova Scotia
B3H 1S6 - Lieu
Publicité
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Lawn Summer Nights
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To date, Lawn Summer Nights has raised over $3,400,000, generated awareness of cystic fibrosis among thousands of people who had little previous exposure to it, introduced thousands of young people to philanthropy and community engagement, and started a new trend that has taken everyone by surprise (us included!).
Founded in 2009, LSN is a nationally trademarked and federally registered not-for-profit organization in Canada. the event is driven by volunteer young professionals who form each city's organizing committee, and supported by a National Manager as well as the Board of Directors. The event currently operates in Victoria, Vancouver, Tsawwassen, Calgary, Edmonton, Regina, Saskatoon, Winnipeg, Windsor, Chatham, Simcoe, London, Brantford, Toronto, Ottawa, Montreal, Charlottetown, and Halifax.
Each city’s event brings together two hundred people in their twenties and thirties throughout July. The participants arrive wearing fun team uniforms that honor creative team names, indulge in delicious menus of food and cocktails, all while reviving one of summertime’s classic leisure sports: lawn bowling.
The Story
Eva Markvoort is our inspiration to support Cystic Fibrosis Canada. Eva spent a lifetime battling cystic fibrosis, but made it her life’s work to build awareness and help to find a cure for the disease. Sadly, Eva lost her own fight with cystic fibrosis on
March 27, 2010.
She was 25 years old. We are proud to be a part of Eva’s legacy and our event will continue to accomplish what Eva championed the most – enjoying life and finding a cure for cystic fibrosis.
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Community Foundation of PEI
The Community Foundation of Prince Edward Island (CFPEI) is an incorporated, non-profit organization that provides a ‘user-friendly’ vehicle for donors to create endowment funds to support charitable activities. Income generated from these investments is directed through grants and scholarships to support a wide range of diverse needs in Prince Edward Island communities. Because of the permanent nature of these endowments, income is available for now and generations to come.
The endowment fund allows the donor to leave a memorial legacy to meet their charitable interests in perpetuity, at minimum cost and maximum convenience. Since its incorporation, the Foundation has worked with donors to establish more than 70 endowment funds; these funds now have a current asset base of over 9 million dollars.
This asset base has allowed the Foundation to grant over 2.5 million dollars to worthy community projects and individual scholarships since 1993. In addition to providing a vehicle for donors to create endowments, the Foundation also has a broader community building and leadership role. Some examples of initiatives undertaken by the Foundation in this role include: the Arts and Heritage Stabilization Program; the ‘Building the Capacity of PEI’s Third Sector’ Report; and the Vital Signs Report ‘Taking the Pulse of Island Youth’.
How we are unique
The Foundation is unique in several ways:
- We are donor focused; each endowment fund is customized to respond to the interests and needs of the donor.
- We are flexible; if the donor interests change over time, the parameters governing the endowment fund can be modified to reflect these new needs.
- Our interests and focus are broad; we have the capacity to respond to and support a wide range of donor and community interests.
- We are a registered charity; we can issue tax receipts for endowments and donations, including tax receipts for donations from US citizens.
Note: Internal Revenue Service (IRS) receipts are of benefit in certain circumstances; US citizens considering making donations should consult with a US tax planner.
Who can benefit
The Foundation can be of benefit to:
- Individuals who wish to honour someone’s legacy by setting up an endowment fund; the fund could be to honour the memory of a family member, or recognize someone who has made a important contribution to his/her community.
- Community groups, organizations, and businesses who have a passion about an issue or concern, or a particular area within the Island community.
- Professional groups and service providers such as lawyers, financial planners, advisors, and accountants who offer estate planning, tax planning, and financial investment services. The Foundation may be an appropriate vehicle to help clients achieve their financial investment, tax planning, and estate planning goals.
- Various levels of governments who find themselves acting as trustees or ‘hosts’ for particular trust or endowment funds; or who wish to recognize the work of a citizen who has made a special contribution to particular initiative, or who has made a significant contribution toward enhancing the quality of life within their own, or the Island, community.
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Canadian Pulmonary Fibrosis Foundation
The Canadian Pulmonary Fibrosis Foundation (CPFF) is a registered Canadian charity established to provide hope and support for people affected by pulmonary fibrosis (PF). Our charitable registration # is 850554858RR0001.
We work closely with patients and caregivers, medical experts, and governments. With the support of dedicated volunteers, staff and our sponsors and donors, we aim to achieve our mission and vision.
We’re Breathless for Change
A relatively common “rare” disease, pulmonary fibrosis affects about 30,000 people in Canada. This number is growing. There is no cure, although there are treatments to slow the progress of the disease. The prognosis for PF is still grim, with most individuals dying within three to five years following diagnosis. And diagnosis can be difficult, taking up to a year or more.
Research is the best prospect for improved treatments and an eventual cure. CPFF offers a community of hope and support to anyone affected by pulmonary fibrosis, so that no one needs to face this disease alone.
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