<p>Participants’ profile.</p>

Introduction
Care involves unequal relationships between gender, corporal conditions and responsibilities. This is especially sensitive for the participation and socio-community inclusion of people with disabilities and their caregivers.
Aim
To analyze the perceptions of caregivers regarding the construction of socio-community care for people with disabilities in the south-central Zone of Chile.
Method
Qualitative study from a situated feminist perspective. Ten semi-structured interviews were conducted with women caregivers of people with disabilities during the years 2021–2022. The interviews were based on qualitative thematic analysis.
Results
The analysis revealed two central categories and six emerging subcategories: a) The world of the system; a.1) Health and rehabilitation, a.2) Education, a.3) Work, and b) The world of life; b.1) Family, b.2) Neighbors and friends, b.3) Community organizations. Socio-community care is a system of action and links that are woven between “The world of the system” and “The world of life” to sustain existence. They are a provision of support and assistance from public institutions and communities.
Conclusions
Socio-community care is built with a lot of effort and exhaustion on the part of the families of people with disabilities, especially by women. Of particular importance is the responsibility and self-organization of communities to meet the needs and care of persons with disabilities. Hence the urgency to develop comprehensive care systems where the State takes greater and better responsibility.