Toolkit

At the June 2020 Alliance Annual General Meeting, Alliance members unanimously passed a resolution to advance sociodemographic data collection in our sector, with a goal of all member organizations having a 75% data completion rate by 2024. Collecting this data is essential to our mission of advancing health equity, because it provides evidence we need to advocate for our clients in priority populations and tailor service delivery to improve care. It also helps us to obtain funding and support for programs that assist our most vulnerable clients.  

At the June 2020 Alliance Annual General Meeting, Alliance members unanimously passed a resolution to advance sociodemographic data collection in our sector, with a goal of all member organizations having a 75% data completion rate by 2024. Collecting this data is essential to our mission of advancing health equity, because it provides evidence we need to advocate for our clients in priority populations and tailor service delivery to improve care. It also helps us to obtain funding and support for programs that assist our most vulnerable clients.  

At the June 2020 Alliance Annual General Meeting, Alliance members unanimously passed a resolution to advance sociodemographic data collection in our sector, with a goal of all member organizations having a 75% data completion rate by 2024. Collecting this data is essential to our mission of advancing health equity, because it provides evidence we need to advocate for our clients in priority populations and tailor service delivery to improve care. It also helps us to obtain funding and support for programs that assist our most vulnerable clients.  

At the June 2020 Alliance Annual General Meeting, Alliance members unanimously passed a resolution to advance sociodemographic data collection in our sector, with a goal of all member organizations having a 75% data completion rate by 2024. Collecting this data is essential to our mission of advancing health equity, because it provides evidence we need to advocate for our clients in priority populations and tailor service delivery to improve care. It also helps us to obtain funding and support for programs that assist our most vulnerable clients.  

This toolkit consists of guidance for healthcare providers as well as an informative patient handout to support access to Paxlovid, a COVID-19 antiviral treatment. 

This toolkit consists of guidance for healthcare providers as well as an informative patient handout to support access to Paxlovid, a COVID-19 antiviral treatment. 

This research project sought to build evidence on community-based and culturally sensitive care pathways for promoting HPV self-sampling-based screening for cervical cancer among under/never-screened women within immigrant communities.

An extensive COVID-19 vaccine resource portal for information about how to advise patients on receiving their vaccinations, educational tools, vaccine efficacy summaries, and more. Check back often as this resource is regularly updated with the latest information for vaccine implementation and rollout.

Help your patients and colleagues make informed choices about COVID-19 vaccination by sharing evidence-based information and resources with them from this toolkit created by the Public Health Agency of Canada. The toolkit is available in both English and French languages.

We are reaching out to you from Indigenous Services Canada (ISC) with the hope that you can help our organization distribute important information among your networks. We are pleased to share the following communications material with you and other organizations that serve the senior population throughout the country. This information highlights the legislative changes to the Indian Act under S-3, and the impact of these changes on First Nations women, children, elders, and communities at large.