“the study showed there are more than 600,000 canadians who are living with dementia from coast to coast in canada and, if nothing were to change, that number will go up to triple in the next 30 years to over 1.7 million people,” wong says. women will continue to outnumber men diagnosed with the disease, but the reason is not fully understood.
what is known is that the older you are, the greater your risk of alzheimer’s, and women tend to live longer than men. genetics may be a risk factor as well. research has shown that people with a parent or sibling with alzheimer’s are more likely to develop the disease.
“not only are we talking about the numbers going up, which means that it will be very commonplace for any one of us to know someone either as a loved one or family member or neighbour or friend who is affected by the condition. it also has an impact on societal health because you can imagine the impact not only within the health sector, but also affecting many other things.”
alzheimer’s disease and the role of the caregiver
wong points to caregiving as a significant part of the alzheimer’s experience that needs to be recognized, as terminology for these individuals is moving from “caregiver” to “care partner” because of the critical role they play in the health-care team.
care partners are often family members or loved ones, but they can also be friends, neighbours, and church parishioners, because many people who develop alzheimer’s are older adults who may be living alone and turn to whomever they can for support. and care partners for people with dementia provide an average of 26 hours of caregiving per week compared to 17 hours per week for older adults with other health issues, according to the landmark study.
“that’s a lot of hours for family care partners,” wong adds, “and that work is unpaid.”