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Abbreviation | ASO |
---|---|
Formation | 1983 |
Type | Alzheimer's disease charity |
Legal status | Active |
Purpose | Advocate, public voice, educator and network |
Headquarters | Toronto, Ontario, Canada |
Region served | Ontario |
Official language | English, French |
Parent organization | Alzheimer Society of Canada |
Website | http://www.alzheimer.ca/en/on/ |
The Alzheimer Society of Ontario (ASO) is a care and research charity committed to helping people living with Alzheimer's disease and other dementias by:
1983: the Alzheimer Society of Ontario is founded by Madeline Honeyman. After her husband was diagnosed with Alzheimer's disease, Honeyman found hundreds of other individuals facing the same issues and problems. She co-founded the ASO as a way to unify the people who were struggling with the disease.
1989: the Alzheimer Society Research Program (ASRP) is launched - a collaborative initiative between the Alzheimer Societies across Canada, partners and donors.
1990: the official opening of the Tanz Centre for Research in Neurodegenerative Diseases established by the University of Toronto with the support of the Alzheimer Society of Ontario. In 1995, Peter St. George-Hyslop at the Tanz Centre would go on to discover two genes, called presenilins, associated with the early onset Alzheimer's disease.
1999: Ontario government announces a provincial Alzheimer Strategy with $68.4 million in funding.
2006: ASO helps launch the Alzheimer Knowledge Exchange (AKE), a web-based forum that links people, ideas and resources to spread the word about innovations in care.
2007: ASO launches First Link, a program connecting people with recent diagnoses of dementia to their local society.
2012: ASO completes a commitment to donate $12 million to the Tanz CRND since it was founded in 1990.
2017: The Province of Ontario commits to a provincial wide dementia strategy led by the minister for seniors. [1]
Staff and volunteers in 30 Alzheimer Societies across Ontario provide support programs, educational resources and referral services to ease the burden of care and improve the quality of life for people living with Alzheimer's disease and other dementias. These include:
Local Societies also host events to promote awareness and raise funds for research. Coffee Break is the Alzheimer Society's major nationwide annual fundraiser where friends, co-workers and customers gather in communities across Canada to raise funds for local Alzheimer Societies. Participants at these events make a donation in exchange for a cup of coffee. The money raised stays in that province or community to help support local programs and services.
Walk for Alzheimer's is Canada's biggest fundraiser for Alzheimer's disease and other dementias. Money raised supports programs and services in communities that improve the quality of life for people living with dementia and their families.
The Alzheimer Society of Ontario develops new programs for people impacted by Alzheimer's disease and other dementias. First Link is an innovative program that gives people with dementia and their caregivers and families a direct connection to information and services in their own communities. Ontarians living with dementia receive information about diagnosis, day-to-day living, and positive approaches to care and how to prepare for the end of life. The program also provides individual support and counselling and links people with the disease to other Alzheimer Society programs and services.
Finding Your Way is a program that raises awareness of the risks of people with dementia going missing and helps to prevent such incidents from occurring. In conjunction with Finding Your Way, Medic Alert: Safely Home helps police find people with dementia who are missing and return them home safely.
Alzheimer's disease and other dementias have the potential to overwhelm Ontario's health-care system. ASO campaigns for improved health and social services and a workforce qualified to support people with dementia. A network of volunteer Dementia Champions across the province supports their requests for greater support for those living with the disease and their families.
Since its foundation, the Alzheimer Society of Ontario has been committed to funding research to bring an end to the disease. The Alzheimer Society Research Program, a collaborative effort between the ASO, Alzheimer Society of Canada and its partners, provides research grants and training awards to support the vital work of Canadian investigators in biomedical research as well as social and psychological aspects of the disease.
The Alzheimer Society Research Program (ASRP) has contributed over $30 million to world class Canadian research, with $12 million dedicated to the Tanz CRND since it was founded in 1990.
Currently, over 200,000 Ontarians over the age of 65 have dementia, and, by 2020, will lead to approximately 250,000 Ontarians - roughly 1 in 10 seniors. Women make up almost three quarters of those who have Alzheimer's disease.
Dementia is the general name for a decline in cognitive abilities that impacts a person's ability to perform everyday activities. This typically involves problems with memory, thinking, and behavior. Aside from memory impairment and a disruption in thought patterns, the most common symptoms include emotional problems, difficulties with language, and decreased motivation. The symptoms may be described as occurring in a continuum over several stages. Dementia ultimately has a significant effect on the individual, caregivers, and on social relationships in general. A diagnosis of dementia requires the observation of a change from a person's usual mental functioning and a greater cognitive decline than what is caused by normal aging.
Alzheimer's Society is a United Kingdom care and research charity for people with dementia and their carers. It operates in England, Wales and Northern Ireland, while its sister charities Alzheimer Scotland and Alzheimer Society of Ireland cover Scotland and the Republic of Ireland respectively.
The Alzheimer's Association was founded by Jerome H. Stone with the help of several family members in Chicago, Illinois. Incorporated on April 10, 1980, as the Alzheimer's Disease and Related Disorders Association, Inc., it is a non-profit American volunteer health organization which focuses on care, support and research for Alzheimer's disease.
The Michael J. Fox Foundation for Parkinson's Research aims to find a cure for Parkinson's disease (PD) founded in 2000 by Michael J. Fox. It concentrates on funding research and ensuring the development of improved therapies for people with Parkinson's.
A caregiver, carer or support worker is a paid or unpaid person who helps an individual with activities of daily living. Caregivers who are members of a care recipient's family or social network, and who may have no specific professional training, are often described as informal caregivers. Caregivers most commonly assist with impairments related to old age, disability, a disease, or a mental disorder.
Alzheimer’s Disease International (ADI) is a not-for-profit, international federation of Alzheimer and dementia associations from around the world. The organization is in official relations with the World Health Organization (WHO). ADI advocates for people living with Alzheimer’s disease and all other types of dementia.
As populations age, caring for people with dementia has become more common. Elderly caregiving may consist of formal care and informal care. Formal care involves the services of community and medical partners, while informal care involves the support of family, friends, and local communities. In most mild-to-medium cases of dementia, the caregiver is a spouse or an adult child. Over the period of time, more professional care in the form of nursing and other supportive care may be required medically, whether at home or in a long-term care facility. There are evidence to show that case management can improve care for individuals with dementia and the experience of their caregivers. Furthermore, case management may reduce overall cost and institutional care in the medium term. Millions of people living in the United States take care of a friend or family member with Alzheimer’s disease or a related dementia.
Family caregivers are “relatives, friends, or neighbors who provide assistance related to an underlying physical or mental disability for at-home care delivery and assist in the activities of daily living (ADLs) who are unpaid and have no formal training to provide those services.”
Alzheimer's disease (AD) is a neurodegenerative disease that usually starts slowly and progressively worsens, and is the cause of 60–70% of cases of dementia. The most common early symptom is difficulty in remembering recent events. As the disease advances, symptoms can include problems with language, disorientation, mood swings, loss of motivation, self-neglect, and behavioral issues. As a person's condition declines, they often withdraw from family and society. Gradually, bodily functions are lost, ultimately leading to death. Although the speed of progression can vary, the typical life expectancy following diagnosis is three to nine years.
The Alzheimer Society of Canada (ASC) is a Canadian health charity for people living with Alzheimer's disease and other dementias. Active in communities right across Canada, the Society partners with Alzheimer Societies in every Canadian province to offer information, support and education programs for people with dementia, their families and caregivers. The Alzheimer Society of Canada acts as the national voice for the thousands of Canadians living with dementia and advocates on their behalf for positive change. The Society also funds young and established Canadian researchers working to find the causes and a cure through the Alzheimer Society Research Program.
Memory Bridge, founded in 2004 as The Foundation for Alzheimer's and Cultural Memory, is an American nonprofit organization that creates programs that connect people with Alzheimer's disease to family, friends, and other people in their local community.
Caregiver syndrome or caregiver stress is a condition that strongly manifests exhaustion, anger, rage, or guilt resulting from unrelieved caring for a chronically ill patient. This condition is not listed in the United States' Diagnostic and Statistical Manual of Mental Disorders, although the term is often used by many healthcare professionals in that country. The equivalent used in many other countries, the ICD-11, does include the condition.
The Alzheimer's Association, Central New York Chapter, incorporated on August 1, 1982, as the Alzheimer's Disease and Related Disorders Association, Inc., is a non-profit voluntary health organization which focuses on care, support and research for Alzheimer's disease. The organization is a chapter affiliated with the national Alzheimer's Association.
The ALS Society of Canada is a registered, not-for-profit Canadian organization. ALS Canada, founded in 1977, is a national voluntary health organization dedicated to the fight against amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, and to providing support for those living with ALS.
The Society for the Arts in Dementia Care is a non-profit organisation, with branches in Canada and Australia, dedicated to knowledge dissemination and education that focuses on improving the quality of lives of seniors living with dementia by using the visual and performing arts.
Chronic disease in Northern Ontario is a population health problem. The population in Northern Ontario experiences worse outcomes on a number of important health indicators, including higher rates of chronic disease compared to the population in the rest of Ontario.
The Alzheimer's Foundation of America (AFA) is an American nonprofit organization based in New York City whose mission is to provide support, services and education to individuals, families and caregivers affected by Alzheimer's disease and related dementias nationwide, and fund research for better treatment and a cure. AFA unites more than 2,000 member organizations from coast-to-coast that are dedicated to meeting the educational, social, emotional and practical needs of individuals with Alzheimer's disease and related illnesses, and their caregivers and families. Member organizations include grassroots Alzheimer's agencies, senior centers, adult daycare center, home healthcare agencies, long-term care residences, research facilities, and other dementia-related groups. AFA holds Charity Navigator's highest rating of 4 stars.
Caregiving by country is the regional variation of caregiving practices as distinguished among countries.
The Alzheimer Society of Ireland is the leading dementia specific service provider in Ireland. The registered offices are located at Blackrock, County Dublin. The Alzheimer Society of Ireland works across the country in the heart of local communities providing dementia specific services and supports and advocating for the rights and needs of all people living with dementia and their carers.
Dementia and Alzheimer's disease in Australia is a major health issue. Alzheimer's disease is the most common type of dementia in Australia. Dementia is an ever-increasing challenge as the population ages and life expectancy increases. As a consequence, there is an expected increase in the number of people with dementia, posing countless challenges to carers and the health and aged care systems. In 2018, an estimated 376,000 people had dementia; this number is expected to increase to 550,000 by 2030 and triple to 900,000 by 2050. The dementia death rate is increasing, resulting in the shift from fourth to second leading cause of death from 2006 to 2015. It is expected to become the leading cause of death over the next number of years. In 2011, it was the fourth leading cause of disease burden and third leading cause of disability burden. This is expected to remain the same until at least 2020.
This article includes a list of general references, but it lacks sufficient corresponding inline citations .(August 2016) |