{"id":6941,"date":"2020-06-01T00:00:00","date_gmt":"2020-06-01T05:00:00","guid":{"rendered":"https:\/\/myeloma.ca\/personal-stories\/jackey-labossiere-2\/"},"modified":"2023-10-03T13:39:23","modified_gmt":"2023-10-03T18:39:23","slug":"jackey-labossiere-2","status":"publish","type":"personal-stories","link":"https:\/\/myeloma.ca\/fr\/temoignages\/jackey-labossiere-2\/","title":{"rendered":"Jackey LaBossiere"},"content":{"rendered":"<p>J\u2019ai re\u00e7u le diagnostic d\u2019un my\u00e9lome en 2016, \u00e0 l\u2019\u00e2ge de 64 ans. J\u2019ai \u00e9t\u00e9 envahie d\u2019un sentiment de solitude, j\u2019avais l\u2019impression d\u2019\u00eatre seule. J\u2019ai contact\u00e9 My\u00e9lome Canada en avril 2018 et nous avons discut\u00e9 de la n\u00e9cessit\u00e9 de cr\u00e9er un groupe de soutien<\/p>\n","protected":false},"featured_media":11723,"template":"","story_types":[43],"class_list":["post-6941","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\/6941","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\/11723"}],"wp:attachment":[{"href":"https:\/\/myeloma.ca\/fr\/wp-json\/wp\/v2\/media?parent=6941"}],"wp:term":[{"taxonomy":"story_types","embeddable":true,"href":"https:\/\/myeloma.ca\/fr\/wp-json\/wp\/v2\/story_types?post=6941"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}