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This article aims to analyse how the COVID\u201019 pandemic has impacted on the delicate balance of these supports. Qualitative research was conducted among people with four types of chronic diseases in France: cystic fibrosis, kidney disease, haemophilia and mental disorders. Data on social support was collected using an innovative methodology combining semi\u2010directive interviews (<jats:italic>n<\/jats:italic>\u00a0=\u00a054) and drawings (<jats:italic>n<\/jats:italic>\u00a0=\u00a032). During the first French lockdown (March\u2013May 2020), the chronically ill were mainly supported by the usual support actors of their primary network: spouse and\/or family. However, the COVID\u201019 health crisis has led to several changes in their support network; health\u2010care professionals diversified their support roles and new supporting actors emerged, especially non\u2010human entities and patient organisations. The chronically ill have received an interweaving of emotional, instrumental and informational, formal and informal and human and non\u2010human support. Our study highlights the multiple and dynamic ties between these types of support and argues in favour of a comprehensive approach to social support of the chronically ill, both in social science theory and in practice of care.<\/jats:p>","DOI":"10.1111\/1467-9566.13845","type":"journal-article","created":{"date-parts":[[2024,9,21]],"date-time":"2024-09-21T14:25:03Z","timestamp":1726928703000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Social support for the chronically ill during lockdown. 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