Learn more about meaningful engagement by downloading the full resource guide: Meaningful engagement of people with dementia: A resource guide. You can also contact your Society for a copy.
Practicing meaningful engagement
"To me, 'meaningful engagement' means being able to actively participate...it is the personal involvement and interaction with others that I find to be most satisfying." – A person living with dementia.
What does meaningful engagement mean?
People living with dementia tell us, "Nothing about us, without us."
They also tell us that their experience working with organizations – regardless of where they live in Canada – is sometimes "uneven," meaning that they are not always included in ways they believe would be beneficial for the organization or that are satisfying for them.
It's one of the Alzheimer Society's guiding principles to recognize the individuality of each person with their own unique life experiences, personality, values, beliefs and opinions – this includes people living with dementia.
Meaningful engagement includes:
- Following a person-centred approach that considers the person living with dementia first;
- Respecting and incorporating the voices of people living with dementia into your organization's processes and goals;
- Organization-wide knowledge and awareness about the effects of dementia on the person, thereby reducing stigma against dementia;
- People living with dementia feeling empowered to have a say in your organization's decisions and policies; and,
- In turn, more involvement from people living with dementia ensuring that your organization is developing information and resources that speak effectively to their experiences and needs.
The benefits of meaningful engagement for the person living with dementia
- Being listened to as an equal.
- A sense of purpose and routine.
- Being offered an appropriate outlet for skills and experiences.
- An increase in self-esteem and sense of accomplishment.
- Being able to address issues related to living with dementia.
- Being offered opportunities to influence policies and programs which can improve quality of life.
- Being able to provide the perspective of the person with dementia and affect decision-making.
The benefits of meaningful engagement for your organization
- Credibility and legitimacy that the organization does, in fact, represent and act as a voice for the needs and interests of people with dementia, their families and care partners.
- Increased capacity by capitalizing on the skills and abilities of persons with dementia.
- Doing work that is increasingly relevant.
- Informed decision-making.
- Ability to identify gaps in services from individuals and families who may benefit from them.
- Provision of appropriate information and services that address real concerns.
- Adding depth to the organization and dispelling myths and stereotypes.
- Staff positively supporting the cause of a better quality of life for people with dementia and their caregivers.
The Advisory Group of people living with dementia
Why was the Advisory Group created?
Learning about a person-centred approach to providing services to people living with dementia and their families has helped the Alzheimer Society recognize the importance of hearing the voices of people with lived experience in our work.
There is also a growing demand to expand the ways in which people living with dementia can and want to contribute to all aspects of the Society’s operations, from decision-making and setting standards to providing input into dementia awareness strategies, programs and services, advocacy efforts and systemic change.
As such, the Alzheimer Society of Canada's Advisory Group of people living with dementia gives a voice to the people we help and support. Through this meaningful engagement, we can better understand and serve their needs.
A brief history of the group
In 2012, the Advisory Group initially formed with the goal of engaging people with lived experience as equal partners in our work. In 2016, the group was reformed to increase membership and to bring more diverse perspectives to the table.
At that time, a notice was sent out across the country inviting people living with dementia to join the new Advisory Group (please note that this group is made up of volunteers). Each applicant was ‘interviewed’ one-on-one to ensure that they were the right fit for this opportunity. If not, they were directed to other volunteer opportunities in the organization.
What the group looks like today
The group has two co-chairs: One being a person living with dementia, the other being a staff member at the Alzheimer Society of Canada. The group meets quarterly by teleconference. Once a year, an in-person meeting is held at our office in Toronto to review the workplan and discuss other ways that the group can partner with us in our work.
Right now, the group consists of members from seven of our 10 provinces. There is one representative from each of these provinces, with the exception of Ontario and B.C., who have two members each. We are always interested in trying to recruit members from the other three provinces as well.
All members of this group are in the early to middle stages of dementia. We are still learning how to ensure that the voices of people in the later stages of dementia are reflected in the work that we do. This is something that we are currently working closely with the Advisory Group on.
While the members of this group use their lived experience to guide us in their work, we also acknowledge that each of these individuals has come to the table with a set of unique skills that they have developed through their careers or life experiences. As a group, we do our best to tap into the skills of each member to maximize our strengths.
The work of the Advisory Group
The Advisory Group is charged with the task of creating a high level, multi-year plan for the formal involvement of people living with dementia in our work. They provide guidance to the Alzheimer Society of Canada in fulfilling its engagement plan; raise awareness of the needs of people with dementia, including the specific needs of people living with early onset and/or early stage dementia; and provide input as requested into our operations.
Their experience and leadership has helped us and many Canadians in a variety of ways. See Examples of meaningful engagement accomplished at the Alzheimer Society, below.
Other ways we engage people with lived experience in our work
People with lived experience of dementia do not have to be members of our Advisory Group in order to engage in our work. We invite people with lived experience to engage in our work in a number of ways, such as:
- Reviewing our educational literature to ensure the information is accurate, relevant and accessible,
- Presenting in partnership with us (for example, training sessions or conference presentations),
- Telling their stories and raising their voices as part of awareness campaigns and
- Participating in the research process through the Alzheimer Society Research Program.
Examples of meaningful engagement accomplished at the Alzheimer Society
Here at the Alzheimer Society, meaningful engagement is reflected in our work. Here are a few examples of campaigns, initiatives and resources that we could not have completed effectively without the input, guidance and consideration from our Advisory Group and other people living with dementia.
“Yes. I live with dementia”: Our three-year nationwide awareness campaign
With stigma identified as our top research priority, the Alzheimer Society of Canada surveyed more than 1,500 Canadians in November 2017 to learn more about their attitudes and beliefs when it comes to Alzheimer’s disease and other dementias. Using the survey results, we developed a three-year multichannel awareness campaign with the goal of increasing understanding of the realities and experiences of Canadians who are affected by dementia.
The cornerstone of the campaign was the powerful, first-person stories of 37 ambassadors from across Canada whose lives have been touched by Alzheimer’s and other dementias in some way, each with the headline: “Yes. I live with dementia. Let me help you understand.” A bilingual digital toolkit was provided to all provincial Societies containing key messages, customizable print materials, radio scripts, social media posts and images, and tips on how to run the campaign locally.
Learn more about Alzheimer's Awareness Month.
The Canadian Dementia Priority Setting Partnership study
In 2017, researchers at the Toronto Rehabilitation Institute, Dr. Jennifer Bethell and Dr. Katherine McGilton, surveyed more than 1,200 Canadians living with dementia, as well as their friends, family, caregivers and healthcare providers. They identified their top 10 dementia research priorities, which will help to inform researchers and research funding organizations as well as the Government of Canada’s national dementia strategy.
The initiative, known as the Canadian Dementia Priority Setting Partnership study, was funded by the Alzheimer Society Research Program as part of our commitment to the Canadian Consortium on Neurodegeneration in Aging (CCNA).
The top priority identified in the study came as a bit of a surprise to researchers: It was understanding the stigmas associated with dementia, their impact, and strategies for reducing them.
Learn more about the the Canadian Dementia Priority Setting Partnership.
The first-ever Canadian Charter of Rights for People with Dementia
As difficult as it is to receive a diagnosis of dementia, people with dementia tell us that it can be even more devastating to experience the stigma of this disease on a daily basis. To protect their human rights and give themselves a voice, the Alzheimer Society of Canada's Advisory Group of People with Dementia created the first-ever Canadian Charter of Rights for People with Dementia in 2018.
The Charter empowers people with dementia to understand and advocate for their rights. It is also meant to help policy makers, health-care professionals and organizations pause and reflect on how they currently interact with people with dementia and consider how they can ensure the rights of people with dementia whom they support are respected.
Learn more about the Canadian Charter of Rights for People with Dementia.
The campaign for Canada's first-ever national dementia strategy
On June 17, 2019, the Government of Canada released the country’s first-ever national dementia strategy: A Dementia Strategy for Canada: Together We Aspire. The strategy will address the overwhelming scale, impact and cost of dementia in Canada through three key objectives:
- Prevent dementia,
- Advance therapies and find a cure, and
- Improve the quality of life of people living with dementia and caregivers.
While our work isn't done yet – the strategy needs to be fully funded for its potential benefits to be thoroughly realized – the Alzheimer Society of Canada recognizes and thanks the people living with dementia who have supported and advocated for the strategy since day one, and have participated as spokespeople in our campaigns to support its creation and implementation.
Learn more about Canada's national dementia strategy.
Our educational resources
Memory tips & tricks: A resource to help people living with mild memory problems
This resource, developed and published in 2018, could not have been written without the contribution, guidance and support of the members of the Alzheimer Society of Canada Advisory Group of people living with dementia.
Read Memory tips & tricks and other helpful routines and reminders.
The development of person-centred language guidelines
In 2017, the Alzheimer Society developed person-centred language guidelines for individuals and organizations to consider when discussing dementia behaviour, people living with dementia and caregivers. Many of the preferred terms in these guidelines come recommended by people living with dementia.
Learn more about using person-centred language guidelines.
Shared experiences: Advice from people living with Alzheimer's disease
This booklet, informed by the real experiences and advice of Canadians living with Alzheimer's disease, can help answer common questions and concerns about living with Alzheimer's. It's divided into seven different sections, each focusing on a different aspect of living with Alzheimer's.
Learn more about Shared experiences for people living with Alzheimer's disease.
Using our resource guide
People living with dementia have a right to be involved in organizations that represent their interests. With this in mind, the Alzheimer Society and the Advisory Group have developed a resource guide for staff and leadership volunteers of all organizations in which people living with dementia are involved.
Our resource guide on meaningful engagement intends to:
- Foster relationship building between staff and leadership volunteers and people with dementia.
- Promote the value-added potential of including the “voices of those with dementia”.
- Improve the experience of meaningful engagement for both the organization and the person with dementia.
- Build capacity within organizations to collaboratively address the needs of persons with dementia.
The content in this resource guide supports the philosophy of person-centered engagement which recognizes that individuals have unique values, personal history and personality and that each person has an equal right to dignity, respect and to participate fully in their environment.