La cartographie du parcours de vie avec la maladie en partenariat avec les patient(e)s et les personnes proches aidantes : un guide méthodologique

This methodological guide (36 pages) is both a reference tool and a practical aid for teams as regards co-building maps of the illness experience with patients, caregivers and the general public.
Year: 2023
Languages: French
Format: Document (article, report, guide, etc.)
Dimension(s) of caregiving:
  • Analysis of caregiving support

Need help? →

CALL 811 (Info-Santé/Info-Social). If you need support or have concerns or questions about your health or that of a family member or friend, call 811 to speak to a nurse or psychosocial worker. Bilingual and available 24 hours a day, 7 days a week, it’s free and confidential.

To speak to a caregiver counselor about a difficult situation, ask questions or get a referral, call l’Appui’s Caregiver Support Helpline.

Bilingual; open Monday to Friday from 8 a.m. to 6 p.m.

1 855 852-7784

[email protected]

www.lappui.org

To find community resources offering caregiving information and support near you, consult l’Appui’s Resource Directory or Proche aidance Québec's list of member organizations (in French only).

!
Image Cartographie du parcours de vie FR - Répertoire

This methodological guide (36 pages, in French) is both a reference tool and a practical aid for teams as regards co-building maps of the illness experience with patients, caregivers and the general public. It was created by the Centre of Excellence for Partnerships with Patients and the Public (CEPPP) and the Unité de Soutien SSA Québec. 

The guide presents two complementary approaches to mapping the lived experience of chronic illness in partnership with patients and caregivers — namely, the life-course-with-illness approach, and care and service trajectories. The document is divided into four sections:  

 

 

  1. Definitions of the concepts used to build a shared understanding of the experience of living with illness and of patient and caregiver experiences. 
  2. Mapping the care and service trajectories and the experience of living with illness 
  3. Methodology (two co-design methods) 
  4. Additional tools and resources