{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T21:11:50Z","timestamp":1790111510063,"version":"4.0.1"},"reference-count":0,"publisher":"JMIR Publications Inc.","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Internet Res"],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    When research, treatment, and support are scarce, where can people living with rare or contested conditions turn? In this\n                    <jats:italic>News and Perspectives<\/jats:italic>\n                    article, JMIR Correspondent Vanessa Nirode reports on the role that online patient support communities play, highlighting People Allergic to Me syndrome as a case study.\n                  <\/jats:p>","DOI":"10.2196\/111170","type":"journal-article","created":{"date-parts":[[2026,9,21]],"date-time":"2026-09-21T18:38:59Z","timestamp":1790015939000},"page":"e111170-e111170","source":"Crossref","is-referenced-by-count":0,"title":["Online Patient Support Communities as Sources of Support, Risk, and Research for Rare or Contested Conditions"],"prefix":"10.2196","volume":"28","author":[{"given":"Vanessa","family":"Nirode","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1010","published-online":{"date-parts":[[2026,9,18]]},"container-title":["Journal of Medical Internet Research"],"original-title":[],"language":"en","deposited":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T20:55:51Z","timestamp":1790110551000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jmir.org\/2026\/1\/e111170"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,9,18]]},"references-count":0,"URL":"https:\/\/doi.org\/10.2196\/111170","relation":{},"ISSN":["1438-8871"],"issn-type":[{"value":"1438-8871","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,9,18]]},"article-number":"v28i1e111170"}}