{"id":6939,"date":"2020-05-01T00:00:00","date_gmt":"2020-05-01T05:00:00","guid":{"rendered":"https:\/\/myeloma.ca\/personal-stories\/ellis-basevitz\/"},"modified":"2023-11-24T09:24:56","modified_gmt":"2023-11-24T14:24:56","slug":"ellis-basevitz","status":"publish","type":"personal-stories","link":"https:\/\/myeloma.ca\/fr\/temoignages\/ellis-basevitz\/","title":{"rendered":"Ellis Basevitz"},"content":{"rendered":"<p>On m\u2019a diagnostiqu\u00e9 un my\u00e9lome multiple en 2005, il y a 15 ans.&nbsp;\u00c0 ce moment, j\u2019ai navigu\u00e9 sur Internet \u00e0 la recherche d\u2019information sur la maladie, et c\u2019est alors que j\u2019ai d\u00e9couvert My\u00e9lome Canada. J\u2019ai contact\u00e9 Aldo Del Col, cofondateur de My\u00e9lome Canada<\/p>\n","protected":false},"featured_media":6938,"template":"","story_types":[43],"class_list":["post-6939","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\/6939","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\/6938"}],"wp:attachment":[{"href":"https:\/\/myeloma.ca\/fr\/wp-json\/wp\/v2\/media?parent=6939"}],"wp:term":[{"taxonomy":"story_types","embeddable":true,"href":"https:\/\/myeloma.ca\/fr\/wp-json\/wp\/v2\/story_types?post=6939"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}