{"id":6923,"date":"2020-01-01T00:00:00","date_gmt":"2020-01-01T05:00:00","guid":{"rendered":"https:\/\/myeloma.ca\/personal-stories\/david-mcmullen\/"},"modified":"2023-11-24T09:25:20","modified_gmt":"2023-11-24T14:25:20","slug":"david-mcmullen","status":"publish","type":"personal-stories","link":"https:\/\/myeloma.ca\/fr\/temoignages\/david-mcmullen\/","title":{"rendered":"David McMullen"},"content":{"rendered":"<p>J\u2019ai re\u00e7u le diagnostic d\u2019un my\u00e9lome en janvier 2012, il y a huit ans. Comme de nombreux patients, j\u2019avais des sympt\u00f4mes bien avant cette date. Heureusement, mon m\u00e9decin de famille a reconnu les sympt\u00f4mes du my\u00e9lome et m\u2019a rapidement dirig\u00e9 vers le Centre<\/p>\n","protected":false},"featured_media":6922,"template":"","story_types":[43],"class_list":["post-6923","personal-stories","type-personal-stories","status-publish","has-post-thumbnail","hentry","story_types-vivre-avec-un-myelome"],"acf":[],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/myeloma.ca\/fr\/wp-json\/wp\/v2\/personal-stories\/6923","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/myeloma.ca\/fr\/wp-json\/wp\/v2\/personal-stories"}],"about":[{"href":"https:\/\/myeloma.ca\/fr\/wp-json\/wp\/v2\/types\/personal-stories"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/myeloma.ca\/fr\/wp-json\/wp\/v2\/media\/6922"}],"wp:attachment":[{"href":"https:\/\/myeloma.ca\/fr\/wp-json\/wp\/v2\/media?parent=6923"}],"wp:term":[{"taxonomy":"story_types","embeddable":true,"href":"https:\/\/myeloma.ca\/fr\/wp-json\/wp\/v2\/story_types?post=6923"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}