Honor their memory with a charitable gift.

For over forty years, The King’s Daughters Dinner Wagon, a not-for-profit agency now known as Meals on Wheels, has been dedicated to providing nutritious meals, daily companionship and comfort with a smile.

The DLC believes that if we foster those positive human qualities that the Dalai Lama inspires in us - like compassion and mindfulness - through holistic learning and life practices, our children will flourish into communities of people who are socially and emotionally equipped to lead fulfilling, peaceful lives. The DLC's role is to: Educate the public, Convene thought leaders and experts, Advise policy makers and other circles of influence, and Apply research that will advance both the knowledge and practice of heart-mind well-being.

The Arthritis Research Centre of Canada (ARC) is an international leader in medical research on Canada’s most debilitating chronic disease. ARC conducts consumer-driven clinical research to help reduce the burden of arthritis, and give people with arthritis better, more timely, and cost-effective solutions for living with their disease. With research centres in British Columbia, Alberta and Quebec, ARC’s research is making a critical difference in arthritis diagnosis, prognosis, prevention, care outcomes and quality of life issues for millions of arthritis patients.

In response to aging CT technology and an increasing need for medical scans, the Foundation is raising $2.5 Million for a new CT Scanner in 2014. Thank you for your generous support!

The Oakville Hospital Foundation raises funds for the Oakville-Trafalgar Memorial Hospital of Halton Healthcare Services. The Foundation strives to ensure Oakville residents have access to the highest quality healthcare services, which government funding alone can not provide. With community support, the Foundation works to ensure essential healthcare services and resources are available today for patients, community and staff and will be there tomorrow to meet the community’s growing needs.

Ontario March of Dimes is one of the largest charitable rehabilitation organizations in Ontario, providing a wide range of services across the province to enhance the independence and community participation of people with physical disabilities. Our consumers include those who have cerebral palsy, spina bifida, muscular dystrophy, multiple sclerosis, Parkinson’s disease, post-polio syndrome, and people who have acquired their disability through injury, or have experienced a stroke. We help people find jobs, acquire wheelchairs and other assistive devices, provide recreation programs to those who are socially isolated, and so much more.

The Heart and Stroke Foundation of Canada is a national voluntary non-profit organization whose mission is to improve the health of Canadians by preventing and reducing disability and death from heart disease and stroke through research, health promotion and advocacy. The Heart and Stroke Foundation of Canada is a federation of 10 provincial Foundations, led and supported by a force of more than 130,000 volunteers. For information on heart disease, stroke and healthy living, call 1-888-HSF-INFO (473-4636) or visit www.heartandstroke.ca

The Alzheimer Society of Ontario’s Today’s Help, Tomorrow’s Cure Campaign is reaching out to the almost 150,000 Ontarians who have Alzheimer's Disease and related dementias (ADRD). By 2031 that number will increase by nearly 127%. That means that we will be caring for over 175,000 cases in 2010 and by 2031 there will be over 340,000 cases in the province. Our goal is to help persons with Alzheimer's Disease and related dementias, their families and caregivers today, while engaging in research to put an end to this devastating disease. With your support we fund nationwide research to address the psychological and social aspects of AD such as care giving, family support and long-term care as well as biomedical investigations to find causes and treatments. The Alzheimer Society of Ontario helps local chapters deliver services by providing consultation as well as financial and educational support. In addition, we assist in program development, fundraising and supportive public policy.

Help our world-class health care professionals pioneer research and deliver "super-specialized" care for the most serious and complex diseases and illnesses adults may ever face. Help fund brand new life-saving technology and groundbreaking research for cures and treatments for people in B.C.

Lupus is a life altering and potentially life-threatening auto-immune disease for which there is no cure. In an autoimmune disease, the body’s immune system (which normally protects and defends the body against disease and illness) becomes overactive, often attacking healthy tissues of the body. It can affect any organ or system. The resultant inflammation can be destructive as well as debilitating. In Ontario, we have increased the number of support centres and assisted volunteers who have helped many people with lupus share information and education to better manage their disease. Lupus Ontario knows that there are not enough specialized physicians to give adequate care to people living with lupus. To address this, we financially support two fellowships that educate in the optimum treatment of people living with lupus. We continue to drive awareness through advocacy, written articles, media releases, PSAs and our updated website. We support research; RESEARCH BRINGS US HOPE

Our two major programs provide hope for the future through the support of MS research into the cause, treatment and cure of the disease and hope for today through our many services that assist people with MS and their families. Eighty-three per cent of the MS Society net revenue is devoted to program areas: MS research, services for people with MS and their families, MS clinics, social action, public education and awareness, and chapter development.

Cassie and Friends was established in 2007 in Vancouver by parents, David Porte and Debbie Setton, along with five other families all affected by Juvenile Arthritis. Cassie was 18-months old when she woke up one morning unable to walk. Soon after, she was diagnosed with Juvenile Idopathic Arthritis. Dealing with the devastating news of his daughter's condition, David was inspired to raise funds for juvenile arthritis by running in the Scotiabank Charity Challenge 5km. He raised over $25,000 in the first year. Since then, through the genrousity of many individuals, families and corporations, Cassie and Friends has raised over $450,000 in support of world-leading research, educational programming, child and family support services and much-needed medical equipment for Juvenile Arthritis sufferers. We look forward to growing our support of the kids and families who suffer daily from this painful disease - and ultimately improving their quality of life and expected outcomes.