{"id":1401,"date":"2026-07-29T15:16:01","date_gmt":"2026-07-29T13:16:01","guid":{"rendered":"https:\/\/amyloidosisalliance.local\/membres-de-lalliance\/"},"modified":"2026-09-29T17:53:20","modified_gmt":"2026-09-29T15:53:20","slug":"membres","status":"publish","type":"page","link":"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/","title":{"rendered":"Membres de l\u2019Alliance"},"content":{"rendered":"\n<nav aria-label=\"Breadcrumb\" class=\"wp-block-group aa-breadcrumb is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"aa-inner\"><a href=\"\/\">Accueil<\/a><span class=\"aa-breadcrumb__sep\">\u203a<\/span><a href=\"https:\/\/www.amyloidosisalliance.org\/about-us\/\">L\u2019Alliance<\/a><span class=\"aa-breadcrumb__sep\">\u203a<\/span><span class=\"aa-breadcrumb__current\">Membres de l\u2019Alliance<\/span><\/div>\n<\/nav>\n\n<section class=\"wp-block-group aa-page-hero is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-inner is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-page-hero__grid is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group is-layout-flow wp-block-group-is-layout-flow\">\n<p class=\"aa-overline wp-block-paragraph\">L\u2019Alliance<\/p>\n\n\n\n<h1 class=\"wp-block-heading\">Membres de l\u2019Alliance<\/h1>\n\n\n\n<p class=\"aa-lead wp-block-paragraph\">Des associations du monde entier. Nos membres sont les organisations de patients qui font de l\u2019Alliance une voix v\u00e9ritablement mondiale dans la lutte contre l\u2019amylose.<\/p>\n\n\n\n<p class=\"aa-page-hero__body wp-block-paragraph\">Chacune accompagne les patients et les familles de son pays, et ensemble elles partagent connaissances, ressources et campagnes par-del\u00e0 les fronti\u00e8res.<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-group aa-page-hero__photo is-layout-flow wp-block-group-is-layout-flow\">\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"582\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/09\/members-1024x582.jpg\" alt=\"\" class=\"wp-image-1174\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/09\/members-1024x582.jpg 1024w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/09\/members-300x171.jpg 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/09\/members-768x437.jpg 768w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/09\/members.jpg 1500w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n<\/div>\n<\/div>\n<\/div>\n<\/section>\n\n<section class=\"wp-block-group aa-section aa-section--cream aa-members-mapsection is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-inner is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-centered-head is-layout-flow wp-block-group-is-layout-flow\">\n<p class=\"aa-eyebrow wp-block-paragraph\">O\u00f9 nous sommes<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Un r\u00e9seau \u00e0 travers le monde<\/h2>\n\n\n\n<div class=\"aa-divider-dot\"><\/div>\n\n\n\n<p class=\"wp-block-paragraph\">Chaque point correspond \u00e0 un pays o\u00f9 une association membre lutte contre l\u2019amylose. Cliquez sur un point pour afficher les organisations qui y sont implant\u00e9es.<\/p>\n<\/div>\n\n\n<div class=\"aa-members-map\" data-points=\"[{&quot;country&quot;:&quot;Spain&quot;,&quot;lat&quot;:40.42,&quot;lng&quot;:-3.7,&quot;members&quot;:[{&quot;title&quot;:&quot;ABeA, Asociaci\\u00f3n Balear en Amiloidosis&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/abea-asociacion-balear-en-amiloidosis\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/abea-logo-150x150.png&quot;},{&quot;title&quot;:&quot;Amilo&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/amilo\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/member-amilo-150x150.jpg&quot;},{&quot;title&quot;:&quot;ASVEA&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/asvea\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/member-asvea-150x150.jpg&quot;}]},{&quot;country&quot;:&quot;Brazil&quot;,&quot;lat&quot;:-15.79,&quot;lng&quot;:-47.88,&quot;members&quot;:[{&quot;title&quot;:&quot;ABPAR, Associa\\u00e7\\u00e3o Brasileira de Amiloidose&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/abpar-associacao-brasileira-de-amiloidose\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/abpar-logo-150x150.png&quot;}]},{&quot;country&quot;:&quot;France&quot;,&quot;lat&quot;:48.86,&quot;lng&quot;:2.35,&quot;members&quot;:[{&quot;title&quot;:&quot;AFCA, Association Fran\\u00e7aise contre l\\u2019Amylose&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/afca-association-francaise-contre-lamylose\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/07\\\/Sans-titre.png&quot;}]},{&quot;country&quot;:&quot;Belgium&quot;,&quot;lat&quot;:50.85,&quot;lng&quot;:4.35,&quot;members&quot;:[{&quot;title&quot;:&quot;Amybel, association belge de l\\u2019amylose&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/amybel-association-belge-de-lamylose\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/amybel-logo-150x150.png&quot;}]},{&quot;country&quot;:&quot;Netherlands&quot;,&quot;lat&quot;:52.37,&quot;lng&quot;:4.9,&quot;members&quot;:[{&quot;title&quot;:&quot;Amylo\\u00efdose Nederland, fondation n\\u00e9erlandaise de l\\u2019amylose&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/amyloidose-nederland-fondation-neerlandaise-de-lamylose\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/Publication-type-e1786715454575-150x150.png&quot;}]},{&quot;country&quot;:&quot;Austria&quot;,&quot;lat&quot;:48.21,&quot;lng&quot;:16.37,&quot;members&quot;:[{&quot;title&quot;:&quot;Amyloidosis Austria, Leben mit Amyloidose&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/amyloidosis-austria-leben-mit-amyloidose\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/Logo_LMA-150x150.jpg&quot;}]},{&quot;country&quot;:&quot;United States&quot;,&quot;lat&quot;:38.91,&quot;lng&quot;:-77.04,&quot;members&quot;:[{&quot;title&quot;:&quot;Amyloidosis Support Groups&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/amyloidosis-support-groups\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/member-amyloidosis-support-groups.png&quot;}]},{&quot;country&quot;:&quot;United Kingdom&quot;,&quot;lat&quot;:51.51,&quot;lng&quot;:-0.13,&quot;members&quot;:[{&quot;title&quot;:&quot;Amyloidosis UK&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/amyloidosis-uk\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/07\\\/Logos-clients-manon-150x150.jpg&quot;}]},{&quot;country&quot;:&quot;Ireland&quot;,&quot;lat&quot;:53.35,&quot;lng&quot;:-6.26,&quot;members&quot;:[{&quot;title&quot;:&quot;ATTR Amyloidosis All Ireland&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/attr-amyloidosis-all-ireland\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/member-attr-amyloidosis-all-ireland-150x150.png&quot;}]},{&quot;country&quot;:&quot;Australia&quot;,&quot;lat&quot;:-35.28,&quot;lng&quot;:149.13,&quot;members&quot;:[{&quot;title&quot;:&quot;Australian Amyloidosis Network&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/australian-amyloidosis-network\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/member-australian-amyloidosis-network.jpg&quot;}]},{&quot;country&quot;:&quot;Canada&quot;,&quot;lat&quot;:45.42,&quot;lng&quot;:-75.7,&quot;members&quot;:[{&quot;title&quot;:&quot;Canadian Amyloidosis Support Network&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/canadian-amyloidosis-support-network\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/CASN-Logo-e1791528721554-150x150.png&quot;},{&quot;title&quot;:&quot;TTR Amyloidosis Canada&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/ttr-amyloidosis-canada\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/member-ttr-amyloidosis-canada-150x150.jpg&quot;}]},{&quot;country&quot;:&quot;Pite\\u00e5, Sweden&quot;,&quot;lat&quot;:65.3172,&quot;lng&quot;:21.4794,&quot;members&quot;:[{&quot;title&quot;:&quot;FaMY Norrbotten&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/famy-norrbotten\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/07\\\/128046091_10159075707486823_2224744946737925810_n-150x150.jpg&quot;}]},{&quot;country&quot;:&quot;Italy&quot;,&quot;lat&quot;:41.9,&quot;lng&quot;:12.5,&quot;members&quot;:[{&quot;title&quot;:&quot;FAMY, Associazione Italiana Amiloidosi Familiare Onlus&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/famy-associazione-italiana-amiloidosi-familiare-onlus\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/member-famy-associazione-italiana-amiloidosi-familiare-onlus.png&quot;}]},{&quot;country&quot;:&quot;Germany&quot;,&quot;lat&quot;:52.52,&quot;lng&quot;:13.4,&quot;members&quot;:[{&quot;title&quot;:&quot;FAP-eV&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/fap-ev\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/member-fap-ev.png&quot;}]},{&quot;country&quot;:&quot;Mexico&quot;,&quot;lat&quot;:19.43,&quot;lng&quot;:-99.13,&quot;members&quot;:[{&quot;title&quot;:&quot;FFAM&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/ffam\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/member-ffam-150x150.png&quot;}]},{&quot;country&quot;:&quot;Colombia&quot;,&quot;lat&quot;:4.71,&quot;lng&quot;:-74.07,&quot;members&quot;:[{&quot;title&quot;:&quot;FUNCOLEHF, Fundaci\\u00f3n Colombiana para Enfermedades Hu\\u00e9rfanas&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/funcolehf-fundacion-colombiana-para-enfermedades-huerfanas\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/funcolehf-logo-150x150.png&quot;}]},{&quot;country&quot;:&quot;South Korea&quot;,&quot;lat&quot;:37.57,&quot;lng&quot;:126.98,&quot;members&quot;:[{&quot;title&quot;:&quot;Hereditary Amyloidosis Hwanwoohoe&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/hereditary-amyloidosis-hwanwoohoe\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/member-hereditary-amyloidosis-hwanwoohoe-150x150.png&quot;}]},{&quot;country&quot;:&quot;Israel&quot;,&quot;lat&quot;:31.78,&quot;lng&quot;:35.22,&quot;members&quot;:[{&quot;title&quot;:&quot;Israel Amyloidosis Association&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/israel-amyloidosis-association\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/israel-amyloidosis-association-logo-150x150.jpg&quot;}]},{&quot;country&quot;:&quot;New Zealand&quot;,&quot;lat&quot;:-41.29,&quot;lng&quot;:174.78,&quot;members&quot;:[{&quot;title&quot;:&quot;NZAPA, New Zealand Amyloidosis Patient Association&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/fr\\\/membres\\\/nzapa-new-zealand-amyloidosis-patient-association\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/nzapa-logo-150x150.png&quot;}]}]\" data-leaflet-js=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/themes\/amyloidosis-alliance\/assets\/vendor\/leaflet\/leaflet.js\" data-leaflet-css=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/themes\/amyloidosis-alliance\/assets\/vendor\/leaflet\/leaflet.css\" data-cluster-js=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/themes\/amyloidosis-alliance\/assets\/vendor\/leaflet-markercluster\/leaflet.markercluster.js\" data-cluster-css=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/themes\/amyloidosis-alliance\/assets\/vendor\/leaflet-markercluster\/MarkerCluster.css\">\n\t\t\t<div class=\"aa-members-map__frame\"><\/div>\n\t\t<\/div><\/div>\n<\/section>\n\n<section id=\"members\" class=\"wp-block-group aa-section aa-section--white aa-members is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-inner is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\n\n<div class=\"wp-block-group aa-centered-head is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\n\n<p class=\"aa-eyebrow wp-block-paragraph\">Des associations du monde entier<\/p>\n\n\t\t\t\n\n<h2 class=\"wp-block-heading\">Les membres de l\u2019Alliance<\/h2>\n\n\t\t\t\n\n<div class=\"aa-divider-dot\"><\/div>\n\n\t\t\t\n\n<p class=\"wp-block-paragraph\">Cliquez sur une organisation pour lire sa pr\u00e9sentation, visiter son site web et trouver ses comptes sur les r\u00e9seaux sociaux.<\/p>\n\n\t\t<\/div>\n\n\t\t<!-- Listing aliment\u00e9 par le CPT \u00ab Membres \u00bb, tri\u00e9 par nom.\n\t\t     Ajouter un membre dans l'admin le fait appara\u00eetre ici. -->\n\t\t\n\n<div class=\"wp-block-query aa-member-grid is-layout-flow wp-block-query-is-layout-flow\">\n\t\t\t\n<ul class=\"wp-block-post-template is-layout-flow wp-block-post-template-is-layout-flow\"><li class=\"wp-block-post post-1827 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/abea-asociacion-balear-en-amiloidosis\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"960\" height=\"1170\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/abea-logo.png\" class=\"attachment-full size-full wp-post-image\" alt=\"ABeA, Asociaci\u00f3n Balear en Amiloidosis\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/abea-logo.png 960w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/abea-logo-246x300.png 246w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/abea-logo-840x1024.png 840w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/abea-logo-768x936.png 768w\" sizes=\"auto, (max-width: 960px) 100vw, 960px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/abea-asociacion-balear-en-amiloidosis\/\" target=\"_self\" >ABeA, Asociaci\u00f3n Balear en Amiloidosis<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Spain<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">L\u2019ABeA est l\u2019association de l\u2019amylose des \u00eeles Bal\u00e9ares, une organisation \u00e0 but non lucratif qui \u0153uvre \u00e0 am\u00e9liorer la qualit\u00e9 de vie des personnes touch\u00e9es par l\u2019amylose et de leurs familles. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/abea-asociacion-balear-en-amiloidosis\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: ABeA, Asociaci\u00f3n Balear en Amiloidosis<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1817 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/abpar-associacao-brasileira-de-amiloidose\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"1280\" height=\"922\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/abpar-logo.png\" class=\"attachment-full size-full wp-post-image\" alt=\"ABPAR, Associa\u00e7\u00e3o Brasileira de Amiloidose\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/abpar-logo.png 1280w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/abpar-logo-300x216.png 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/abpar-logo-1024x738.png 1024w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/abpar-logo-768x553.png 768w\" sizes=\"auto, (max-width: 1280px) 100vw, 1280px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/abpar-associacao-brasileira-de-amiloidose\/\" target=\"_self\" >ABPAR, Associa\u00e7\u00e3o Brasileira de Amiloidose<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Brazil<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">Fond\u00e9e en 1989, l\u2019ABPAR (Associa\u00e7\u00e3o Brasileira de Amiloidose) est une organisation \u00e0 but non lucratif qui soutient les patients et les familles en faisant conna\u00eetre l\u2019amylose, en informant et en plaidant pour leur cause.\u2026 <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/abpar-associacao-brasileira-de-amiloidose\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: ABPAR, Associa\u00e7\u00e3o Brasileira de Amiloidose<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1832 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/afca-association-francaise-contre-lamylose\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"150\" height=\"150\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/07\/Sans-titre.png\" class=\"attachment-full size-full wp-post-image\" alt=\"AFCA, Association Fran\u00e7aise contre l\u2019Amylose\" style=\"object-fit:contain;\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/afca-association-francaise-contre-lamylose\/\" target=\"_self\" >AFCA, Association Fran\u00e7aise contre l\u2019Amylose<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">France<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">L\u2019Association Fran\u00e7aise contre l\u2019Amylose r\u00e9unit des patients, des familles et des aidants touch\u00e9s par l\u2019amylose en France. Elle informe et accompagne les patients nouvellement diagnostiqu\u00e9s et travaille aux c\u00f4t\u00e9s des professionnels de sant\u00e9 pour\u2026 <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/afca-association-francaise-contre-lamylose\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: AFCA, Association Fran\u00e7aise contre l\u2019Amylose<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1775 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amilo\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"1080\" height=\"1080\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-amilo.jpg\" class=\"attachment-full size-full wp-post-image\" alt=\"Amilo\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-amilo.jpg 1080w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-amilo-300x300.jpg 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-amilo-1024x1024.jpg 1024w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-amilo-150x150.jpg 150w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-amilo-768x768.jpg 768w\" sizes=\"auto, (max-width: 1080px) 100vw, 1080px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amilo\/\" target=\"_self\" >Amilo<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Spain<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">Amilo est une organisation de patients qui agit pour les personnes vivant avec l\u2019amylose et leurs familles (Spain), et membre de l\u2019Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amilo\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: Amilo<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1821 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amybel-association-belge-de-lamylose\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"1280\" height=\"417\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/amybel-logo.png\" class=\"attachment-full size-full wp-post-image\" alt=\"Amybel, association belge de l\u2019amylose\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/amybel-logo.png 1280w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/amybel-logo-300x98.png 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/amybel-logo-1024x334.png 1024w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/amybel-logo-768x250.png 768w\" sizes=\"auto, (max-width: 1280px) 100vw, 1280px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amybel-association-belge-de-lamylose\/\" target=\"_self\" >Amybel, association belge de l\u2019amylose<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Belgium<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">Amybel est une association de patients jeune mais en pleine croissance, pour les personnes atteintes de toutes les formes d\u2019amylose en Belgique. Elle se concentre sur le soutien et l\u2019information des patients et sur\u2026 <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amybel-association-belge-de-lamylose\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: Amybel, association belge de l\u2019amylose<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1801 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidose-nederland-fondation-neerlandaise-de-lamylose\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"430\" height=\"198\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/Publication-type-e1786715454575.png\" class=\"attachment-full size-full wp-post-image\" alt=\"Amylo\u00efdose Nederland, fondation n\u00e9erlandaise de l\u2019amylose\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/Publication-type-e1786715454575.png 430w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/Publication-type-e1786715454575-300x138.png 300w\" sizes=\"auto, (max-width: 430px) 100vw, 430px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidose-nederland-fondation-neerlandaise-de-lamylose\/\" target=\"_self\" >Amylo\u00efdose Nederland, fondation n\u00e9erlandaise de l\u2019amylose<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Netherlands<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">La Fondation n\u00e9erlandaise de l\u2019amylose (Stichting Amylo\u00efdose Nederland) d\u00e9fend les int\u00e9r\u00eats des patients atteints d\u2019amylose. Pour cela, elle fournit des informations fiables sur la maladie aux patients comme aux professionnels, organise des rencontres pour\u2026 <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidose-nederland-fondation-neerlandaise-de-lamylose\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: Amylo\u00efdose Nederland, fondation n\u00e9erlandaise de l\u2019amylose<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1814 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidosis-austria-leben-mit-amyloidose\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"1807\" height=\"511\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/Logo_LMA.jpg\" class=\"attachment-full size-full wp-post-image\" alt=\"Amyloidosis Austria, Leben mit Amyloidose\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/Logo_LMA.jpg 1807w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/Logo_LMA-300x85.jpg 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/Logo_LMA-1024x290.jpg 1024w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/Logo_LMA-768x217.jpg 768w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/Logo_LMA-1536x434.jpg 1536w\" sizes=\"auto, (max-width: 1807px) 100vw, 1807px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidosis-austria-leben-mit-amyloidose\/\" target=\"_self\" >Amyloidosis Austria, Leben mit Amyloidose<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Austria<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">Leben mit Amyloidose \u2013 Amyloidosis Austria est une organisation nationale, dirig\u00e9e par des patients, qui soutient les personnes vivant avec l\u2019amylose et leurs familles. Fond\u00e9e en 2019, elle s\u2019engage \u00e0 sensibiliser, \u00e0 favoriser un\u2026 <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidosis-austria-leben-mit-amyloidose\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: Amyloidosis Austria, Leben mit Amyloidose<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1790 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidosis-support-groups\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"150\" height=\"150\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-amyloidosis-support-groups.png\" class=\"attachment-full size-full wp-post-image\" alt=\"Amyloidosis Support Groups\" style=\"object-fit:contain;\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidosis-support-groups\/\" target=\"_self\" >Amyloidosis Support Groups<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">United States<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">Amyloidosis Support Groups est une organisation de patients qui agit pour les personnes vivant avec l\u2019amylose et leurs familles (the United States), et membre de l\u2019Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidosis-support-groups\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: Amyloidosis Support Groups<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1824 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidosis-uk\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"500\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/07\/Logos-clients-manon.jpg\" class=\"attachment-full size-full wp-post-image\" alt=\"Amyloidosis UK\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/07\/Logos-clients-manon.jpg 500w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/07\/Logos-clients-manon-300x300.jpg 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/07\/Logos-clients-manon-150x150.jpg 150w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidosis-uk\/\" target=\"_self\" >Amyloidosis UK<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">United Kingdom<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">Amyloidosis UK est une association caritative dirig\u00e9e par des patients, qui relie les personnes, partage les connaissances, d\u00e9fend les personnes touch\u00e9es par l\u2019amylose et fait conna\u00eetre la maladie dans tout le Royaume-Uni. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/amyloidosis-uk\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: Amyloidosis UK<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1796 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/asvea\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"359\" height=\"359\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-asvea.jpg\" class=\"attachment-full size-full wp-post-image\" alt=\"ASVEA\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-asvea.jpg 359w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-asvea-300x300.jpg 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-asvea-150x150.jpg 150w\" sizes=\"auto, (max-width: 359px) 100vw, 359px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/asvea\/\" target=\"_self\" >ASVEA<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Spain<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">ASVEA est une organisation de patients qui agit pour les personnes vivant avec l\u2019amylose et leurs familles (Spain), et membre de l\u2019Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/asvea\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: ASVEA<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1793 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/attr-amyloidosis-all-ireland\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"500\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-attr-amyloidosis-all-ireland.png\" class=\"attachment-full size-full wp-post-image\" alt=\"ATTR Amyloidosis All Ireland\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-attr-amyloidosis-all-ireland.png 500w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-attr-amyloidosis-all-ireland-300x300.png 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-attr-amyloidosis-all-ireland-150x150.png 150w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/attr-amyloidosis-all-ireland\/\" target=\"_self\" >ATTR Amyloidosis All Ireland<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Ireland<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">ATTR Amyloidosis All Ireland est une organisation de patients qui agit pour les personnes vivant avec l\u2019amylose et leurs familles (Ireland), et membre de l\u2019Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/attr-amyloidosis-all-ireland\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: ATTR Amyloidosis All Ireland<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1769 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/australian-amyloidosis-network\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"150\" height=\"150\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-australian-amyloidosis-network.jpg\" class=\"attachment-full size-full wp-post-image\" alt=\"Australian Amyloidosis Network\" style=\"object-fit:contain;\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/australian-amyloidosis-network\/\" target=\"_self\" >Australian Amyloidosis Network<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Australia<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">Australian Amyloidosis Network est une organisation de patients qui agit pour les personnes vivant avec l\u2019amylose et leurs familles (Australia), et membre de l\u2019Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/australian-amyloidosis-network\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: Australian Amyloidosis Network<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1787 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/canadian-amyloidosis-support-network\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"553\" height=\"268\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/CASN-Logo-e1791528721554.png\" class=\"attachment-full size-full wp-post-image\" alt=\"Canadian Amyloidosis Support Network\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/CASN-Logo-e1791528721554.png 553w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/CASN-Logo-e1791528721554-300x145.png 300w\" sizes=\"auto, (max-width: 553px) 100vw, 553px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/canadian-amyloidosis-support-network\/\" target=\"_self\" >Canadian Amyloidosis Support Network<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Canada<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">Canadian Amyloidosis Support Network, Inc est un organisme sans but lucratif, enti\u00e8rement b\u00e9n\u00e9vole et enregistr\u00e9 au niveau f\u00e9d\u00e9ral, qui s\u2019engage \u00e0 faire une diff\u00e9rence positive dans la vie des patients et des aidants naturels\u2026 <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/canadian-amyloidosis-support-network\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: Canadian Amyloidosis Support Network<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1835 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/famy-norrbotten\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"1500\" height=\"1500\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/07\/128046091_10159075707486823_2224744946737925810_n.jpg\" class=\"attachment-full size-full wp-post-image\" alt=\"FaMY Norrbotten\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/07\/128046091_10159075707486823_2224744946737925810_n.jpg 1500w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/07\/128046091_10159075707486823_2224744946737925810_n-300x300.jpg 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/07\/128046091_10159075707486823_2224744946737925810_n-1024x1024.jpg 1024w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/07\/128046091_10159075707486823_2224744946737925810_n-150x150.jpg 150w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/07\/128046091_10159075707486823_2224744946737925810_n-768x768.jpg 768w\" sizes=\"auto, (max-width: 1500px) 100vw, 1500px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/famy-norrbotten\/\" target=\"_self\" >FaMY Norrbotten<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Sweden<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">FaMY Norrbotten soutient les patients et les familles qui vivent avec l\u2019amylose h\u00e9r\u00e9ditaire \u00e0 transthyr\u00e9tine dans le nord de la Su\u00e8de, o\u00f9 la maladie est particuli\u00e8rement pr\u00e9sente. L\u2019association organise des rencontres entre patients et\u2026 <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/famy-norrbotten\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: FaMY Norrbotten<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1778 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/famy-associazione-italiana-amiloidosi-familiare-onlus\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"150\" height=\"150\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-famy-associazione-italiana-amiloidosi-familiare-onlus.png\" class=\"attachment-full size-full wp-post-image\" alt=\"FAMY, Associazione Italiana Amiloidosi Familiare Onlus\" style=\"object-fit:contain;\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/famy-associazione-italiana-amiloidosi-familiare-onlus\/\" target=\"_self\" >FAMY, Associazione Italiana Amiloidosi Familiare Onlus<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Italy<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">FAMY est une organisation de patients qui agit pour les personnes vivant avec l\u2019amylose et leurs familles (Italy), et membre de l\u2019Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/famy-associazione-italiana-amiloidosi-familiare-onlus\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: FAMY, Associazione Italiana Amiloidosi Familiare Onlus<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1781 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/fap-ev\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"150\" height=\"150\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-fap-ev.png\" class=\"attachment-full size-full wp-post-image\" alt=\"FAP-eV\" style=\"object-fit:contain;\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/fap-ev\/\" target=\"_self\" >FAP-eV<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Germany<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">FAP-eV est une organisation de patients qui agit pour les personnes vivant avec l\u2019amylose et leurs familles (Germany), et membre de l\u2019Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/fap-ev\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: FAP-eV<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1798 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/ffam\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"800\" height=\"800\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-ffam.png\" class=\"attachment-full size-full wp-post-image\" alt=\"FFAM\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-ffam.png 800w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-ffam-300x300.png 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-ffam-150x150.png 150w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-ffam-768x768.png 768w\" sizes=\"auto, (max-width: 800px) 100vw, 800px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/ffam\/\" target=\"_self\" >FFAM<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Mexico<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">FFAM est une organisation de patients qui agit pour les personnes vivant avec l\u2019amylose et leurs familles (Mexico), et membre de l\u2019Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/ffam\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: FFAM<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1807 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/funcolehf-fundacion-colombiana-para-enfermedades-huerfanas\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"960\" height=\"960\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/funcolehf-logo.png\" class=\"attachment-full size-full wp-post-image\" alt=\"FUNCOLEHF, Fundaci\u00f3n Colombiana para Enfermedades Hu\u00e9rfanas\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/funcolehf-logo.png 960w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/funcolehf-logo-300x300.png 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/funcolehf-logo-150x150.png 150w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/funcolehf-logo-768x768.png 768w\" sizes=\"auto, (max-width: 960px) 100vw, 960px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/funcolehf-fundacion-colombiana-para-enfermedades-huerfanas\/\" target=\"_self\" >FUNCOLEHF, Fundaci\u00f3n Colombiana para Enfermedades Hu\u00e9rfanas<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Colombia<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">La Fundaci\u00f3n Colombiana para Enfermedades Hu\u00e9rfanas (FUNCOLEHF) est une fondation \u00e0 but non lucratif qui \u0153uvre \u00e0 am\u00e9liorer la qualit\u00e9 de vie et l\u2019esp\u00e9rance de vie des personnes et des familles touch\u00e9es par des\u2026 <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/funcolehf-fundacion-colombiana-para-enfermedades-huerfanas\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: FUNCOLEHF, Fundaci\u00f3n Colombiana para Enfermedades Hu\u00e9rfanas<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1772 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/hereditary-amyloidosis-hwanwoohoe\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"1230\" height=\"1126\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-hereditary-amyloidosis-hwanwoohoe.png\" class=\"attachment-full size-full wp-post-image\" alt=\"Hereditary Amyloidosis Hwanwoohoe\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-hereditary-amyloidosis-hwanwoohoe.png 1230w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-hereditary-amyloidosis-hwanwoohoe-300x275.png 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-hereditary-amyloidosis-hwanwoohoe-1024x937.png 1024w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-hereditary-amyloidosis-hwanwoohoe-768x703.png 768w\" sizes=\"auto, (max-width: 1230px) 100vw, 1230px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/hereditary-amyloidosis-hwanwoohoe\/\" target=\"_self\" >Hereditary Amyloidosis Hwanwoohoe<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">South Korea<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">Hereditary Amyloidosis Hwanwoohoe est une organisation de patients qui agit pour les personnes vivant avec l\u2019amylose et leurs familles (South Korea), et membre de l\u2019Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/hereditary-amyloidosis-hwanwoohoe\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: Hereditary Amyloidosis Hwanwoohoe<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1804 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/israel-amyloidosis-association\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"1042\" height=\"223\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/israel-amyloidosis-association-logo.jpg\" class=\"attachment-full size-full wp-post-image\" alt=\"Israel Amyloidosis Association\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/israel-amyloidosis-association-logo.jpg 1042w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/israel-amyloidosis-association-logo-300x64.jpg 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/israel-amyloidosis-association-logo-1024x219.jpg 1024w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/israel-amyloidosis-association-logo-768x164.jpg 768w\" sizes=\"auto, (max-width: 1042px) 100vw, 1042px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/israel-amyloidosis-association\/\" target=\"_self\" >Israel Amyloidosis Association<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Israel<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">L\u2019Israel Amyloidosis Association a \u00e9t\u00e9 fond\u00e9e en 2016 par un groupe de patients atteints d\u2019amylose AL, par esprit de partenariat et de responsabilit\u00e9, et avec la conviction que les patients et leurs familles doivent\u2026 <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/israel-amyloidosis-association\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: Israel Amyloidosis Association<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1810 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/nzapa-new-zealand-amyloidosis-patient-association\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"960\" height=\"960\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/nzapa-logo.png\" class=\"attachment-full size-full wp-post-image\" alt=\"NZAPA, New Zealand Amyloidosis Patient Association\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/nzapa-logo.png 960w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/nzapa-logo-300x300.png 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/nzapa-logo-150x150.png 150w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/nzapa-logo-768x768.png 768w\" sizes=\"auto, (max-width: 960px) 100vw, 960px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/nzapa-new-zealand-amyloidosis-patient-association\/\" target=\"_self\" >NZAPA, New Zealand Amyloidosis Patient Association<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">New Zealand<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">La New Zealand Amyloidosis Patient Association (NZAPA) est une organisation \u00e0 but non lucratif qui \u0153uvre \u00e0 am\u00e9liorer la vie des personnes touch\u00e9es par toutes les formes d\u2019amylose, par la sensibilisation, l\u2019information, le plaidoyer\u2026 <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/nzapa-new-zealand-amyloidosis-patient-association\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: NZAPA, New Zealand Amyloidosis Patient Association<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-1784 aa_member type-aa_member status-publish has-post-thumbnail hentry\">\n\n<div class=\"wp-block-group aa-member-card is-layout-flow wp-block-group-is-layout-flow\">\n\t\t\t\t\n<figure class=\"aa-member-card__logo wp-block-post-featured-image\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/ttr-amyloidosis-canada\/\" target=\"_self\" ><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"500\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-ttr-amyloidosis-canada.jpg\" class=\"attachment-full size-full wp-post-image\" alt=\"TTR Amyloidosis Canada\" style=\"object-fit:contain;\" srcset=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-ttr-amyloidosis-canada.jpg 500w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-ttr-amyloidosis-canada-300x300.jpg 300w, https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/08\/member-ttr-amyloidosis-canada-150x150.jpg 150w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/><\/a><\/figure>\n\t\t\t\t\n<h3 class=\"aa-member-card__name wp-block-post-title\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/ttr-amyloidosis-canada\/\" target=\"_self\" >TTR Amyloidosis Canada<\/a><\/h3>\n\t\t\t\t\n\n<p class=\"aa-member-card__country wp-block-paragraph\">Canada<\/p>\n\n\t\t\t\t\n<div class=\"aa-member-card__intro wp-block-post-excerpt\"><p class=\"wp-block-post-excerpt__excerpt\">TTR Amyloidosis Canada est une organisation de patients qui agit pour les personnes vivant avec l\u2019amylose et leurs familles (Canada), et membre de l\u2019Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/ttr-amyloidosis-canada\/\" target=\"_self\">En savoir plus<span class=\"screen-reader-text\">\u00a0: TTR Amyloidosis Canada<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><\/ul>\n\t\t\t\n\n\t\t<\/div>\n\n\t\t\n\n<p class=\"aa-members__note wp-block-paragraph\">Nos membres sont les associations nationales de patients qui composent le r\u00e9seau. Ils se distinguent de nos partenaires, les entreprises et institutions qui soutiennent le travail de l\u2019Alliance.<\/p>\n\n\t<\/div>\n<\/section>\n\n<section id=\"become-a-member\" class=\"wp-block-group aa-section aa-section--cream aa-become is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-inner is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-columns aa-become__grid is-layout-flex wp-container-core-columns-is-layout-b2e659ba wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:48%\">\n<p class=\"aa-section-num wp-block-paragraph\">Devenir membre<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Votre organisation ne figure pas dans cette liste\u202f?<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">Les organisations de patients qui luttent contre l\u2019amylose, partout dans le monde, sont invit\u00e9es \u00e0 d\u00e9poser leur candidature. Les organisations cr\u00e9\u00e9es depuis moins d\u2019un an rejoignent l\u2019Alliance comme membres associ\u00e9s, le temps de trouver leurs marques.<\/p>\n\n\n\n<div class=\"wp-block-buttons aa-become__cta is-layout-flex wp-block-buttons-is-layout-flex\">\n<div class=\"wp-block-button aa-btn aa-btn--primary\"><a class=\"wp-block-button__link wp-element-button\" href=\"#apply\">Demander \u00e0 rejoindre l\u2019Alliance<\/a><\/div>\n<\/div>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:52%\">\n<div class=\"wp-block-group aa-checklist is-layout-flow wp-block-group-is-layout-flow\">\n<h3 class=\"wp-block-heading\">Comment \u00e7a marche<\/h3>\n\n\n\n<ul class=\"wp-block-list aa-checklist__items\">\n<li>Envoyez-nous une courte demande \u00e0 l\u2019aide du formulaire ci-dessous.<\/li>\n\n\n\n<li>Nous organisons un \u00e9change avec une personne de l\u2019Alliance, pour parler de votre organisation, de vos projets et de l\u00e0 o\u00f9 vous en \u00eates aujourd\u2019hui.<\/li>\n\n\n\n<li>Nous vous demandons ensuite une courte pr\u00e9sentation de votre organisation (3 \u00e0 4 lignes), l\u2019adresse de votre site web, les liens vers vos comptes sur les r\u00e9seaux sociaux, une brochure de pr\u00e9sentation au format PDF si vous en avez une, et votre logo au format PNG en haute qualit\u00e9, de pr\u00e9f\u00e9rence sur fond transparent.<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/section>\n\n<section id=\"apply\" class=\"wp-block-group aa-section aa-section--white aa-formsection is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-inner is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-formsection__panel is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-centered-head is-layout-flow wp-block-group-is-layout-flow\">\n<p class=\"aa-eyebrow wp-block-paragraph\">Demande d\u2019adh\u00e9sion<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Demander \u00e0 rejoindre l\u2019Alliance<\/h2>\n\n\n\n<div class=\"aa-divider-dot\"><\/div>\n\n\n\n<p class=\"wp-block-paragraph\">Pr\u00e9sentez-nous votre organisation. Une personne de l\u2019Alliance reviendra vers vous pour organiser un \u00e9change.<\/p>\n<\/div>\n\n\n\n<div class=\"wpcf7 no-js\" id=\"wpcf7-f1889-o1\" lang=\"fr-FR\" dir=\"ltr\" data-wpcf7-id=\"1889\">\n<div class=\"screen-reader-response\"><p role=\"status\" aria-live=\"polite\" aria-atomic=\"true\"><\/p> <ul><\/ul><\/div>\n<form action=\"\/fr\/wp-json\/wp\/v2\/pages\/1401#wpcf7-f1889-o1\" method=\"post\" class=\"wpcf7-form init\" aria-label=\"Formulaire de contact\" novalidate=\"novalidate\" data-status=\"init\">\n<fieldset class=\"hidden-fields-container\"><input type=\"hidden\" name=\"_wpcf7\" value=\"1889\" \/><input type=\"hidden\" name=\"_wpcf7_version\" value=\"6.1.7\" \/><input type=\"hidden\" name=\"_wpcf7_locale\" value=\"fr_FR\" \/><input type=\"hidden\" name=\"_wpcf7_unit_tag\" value=\"wpcf7-f1889-o1\" \/><input type=\"hidden\" name=\"_wpcf7_container_post\" value=\"0\" \/><input type=\"hidden\" name=\"_wpcf7_posted_data_hash\" value=\"\" \/>\n<\/fieldset>\n<div class=\"aa-form__grid\">\n\t<p class=\"aa-form__field\"><label for=\"aa-join-name\">Votre nom <span class=\"aa-form__req\">*<\/span><\/label><br \/>\n<span class=\"wpcf7-form-control-wrap\" data-name=\"your-name\"><input size=\"40\" maxlength=\"400\" class=\"wpcf7-form-control wpcf7-text wpcf7-validates-as-required\" id=\"aa-join-name\" autocomplete=\"name\" aria-required=\"true\" aria-invalid=\"false\" value=\"\" type=\"text\" name=\"your-name\" \/><\/span>\n\t<\/p>\n\t<p class=\"aa-form__field\"><label for=\"aa-join-email\">Votre e-mail <span class=\"aa-form__req\">*<\/span><\/label><br \/>\n<span class=\"wpcf7-form-control-wrap\" data-name=\"your-email\"><input size=\"40\" maxlength=\"400\" class=\"wpcf7-form-control wpcf7-email wpcf7-validates-as-required wpcf7-text wpcf7-validates-as-email\" id=\"aa-join-email\" autocomplete=\"email\" aria-required=\"true\" aria-invalid=\"false\" value=\"\" type=\"email\" name=\"your-email\" \/><\/span>\n\t<\/p>\n\t<p class=\"aa-form__field\"><label for=\"aa-join-org\">Votre organisation <span class=\"aa-form__req\">*<\/span><\/label><br \/>\n<span class=\"wpcf7-form-control-wrap\" data-name=\"organisation\"><input size=\"40\" maxlength=\"400\" class=\"wpcf7-form-control wpcf7-text wpcf7-validates-as-required\" id=\"aa-join-org\" aria-required=\"true\" aria-invalid=\"false\" value=\"\" type=\"text\" name=\"organisation\" \/><\/span>\n\t<\/p>\n\t<p class=\"aa-form__field\"><label for=\"aa-join-country\">Pays <span class=\"aa-form__req\">*<\/span><\/label><br \/>\n<span class=\"wpcf7-form-control-wrap\" data-name=\"country\"><input size=\"40\" maxlength=\"400\" class=\"wpcf7-form-control wpcf7-text wpcf7-validates-as-required\" id=\"aa-join-country\" autocomplete=\"country-name\" aria-required=\"true\" aria-invalid=\"false\" value=\"\" type=\"text\" name=\"country\" \/><\/span>\n\t<\/p>\n<\/div>\n<p class=\"aa-form__field\"><label for=\"aa-join-website\">Le site web de votre organisation<\/label><br \/>\n<span class=\"wpcf7-form-control-wrap\" data-name=\"website\"><input size=\"40\" maxlength=\"400\" class=\"wpcf7-form-control wpcf7-url wpcf7-text wpcf7-validates-as-url\" id=\"aa-join-website\" aria-invalid=\"false\" placeholder=\"https:\/\/\" value=\"\" type=\"url\" name=\"website\" \/><\/span>\n<\/p>\n<p class=\"aa-form__field\"><label for=\"aa-join-message\">Pr\u00e9sentez-nous votre organisation<\/label><br \/>\n<span class=\"wpcf7-form-control-wrap\" data-name=\"your-message\"><textarea cols=\"40\" rows=\"6\" maxlength=\"2000\" class=\"wpcf7-form-control wpcf7-textarea\" id=\"aa-join-message\" aria-invalid=\"false\" name=\"your-message\"><\/textarea><\/span>\n<\/p>\n<p class=\"aa-form__consent\"><span class=\"wpcf7-form-control-wrap\" data-name=\"consent\"><span class=\"wpcf7-form-control wpcf7-acceptance\"><span class=\"wpcf7-list-item\"><label><input type=\"checkbox\" name=\"consent\" value=\"1\" aria-invalid=\"false\" \/><span class=\"wpcf7-list-item-label\">J\u2019accepte que les informations transmises par ce formulaire soient utilis\u00e9es par l\u2019Amyloidosis Alliance pour traiter ma demande. Elles ne seront jamais transmises \u00e0 des tiers.<\/span><\/label><\/span><\/span><\/span>\n<\/p>\n<div class=\"wpcf7-turnstile cf-turnstile\" data-sitekey=\"0x4AAAAAAFDaUgHfDVUpK-9I\" data-response-field-name=\"_wpcf7_turnstile_response\"><\/div>\n<p class=\"aa-form__submit\"><input class=\"wpcf7-form-control wpcf7-submit has-spinner aa-form__button\" type=\"submit\" value=\"Envoyer votre candidature\" \/>\n<\/p><div class=\"wpcf7-response-output\" aria-hidden=\"true\"><\/div>\n<\/form>\n<\/div>\n\n<\/div>\n<\/div>\n<\/section>\n\n<section class=\"wp-block-group aa-next aa-next--split is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-inner is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-next__head is-layout-flow wp-block-group-is-layout-flow\">\n<p class=\"aa-section-num wp-block-paragraph\">Aller plus loin<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">L\u2019Alliance<\/h2>\n<\/div>\n\n\n\n<div class=\"wp-block-group aa-next__grid is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-group aa-next-card is-layout-flow wp-block-group-is-layout-flow\">\n<h3 class=\"wp-block-heading\"><a href=\"https:\/\/www.amyloidosisalliance.org\/about-us\/\">\u00c0 propos<\/a><\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Qui nous sommes, comment l\u2019Alliance est n\u00e9e et ce qui rassemble nos membres.<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-group aa-next-card is-layout-flow wp-block-group-is-layout-flow\">\n<h3 class=\"wp-block-heading\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/nos-partenaires\/\">Nos partenaires<\/a><\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Les entreprises et institutions dont le soutien nous aide \u00e0 mener nos projets dans le monde entier.<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-group aa-next-card is-layout-flow wp-block-group-is-layout-flow\">\n<h3 class=\"wp-block-heading\"><a href=\"https:\/\/www.amyloidosisalliance.org\/fr\/nous-rejoindre\/\">Nous rejoindre<\/a><\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Faites entrer votre association dans le r\u00e9seau et luttez contre l\u2019amylose \u00e0 nos c\u00f4t\u00e9s.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/section>\n","protected":false},"excerpt":{"rendered":"<p>Accueil\u203aL\u2019Alliance\u203aMembres de l\u2019Alliance L\u2019Alliance Membres de l\u2019Alliance Des associations du monde entier. Nos membres sont les organisations de patients qui font de l\u2019Alliance une voix v\u00e9ritablement mondiale dans la lutte contre l\u2019amylose. Chacune accompagne les patients et les familles de son pays, et ensemble elles partagent connaissances, ressources et campagnes par-del\u00e0 les fronti\u00e8res. O\u00f9 nous [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-1401","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Organisations de patients atteints d\u2019amylose dans le monde<\/title>\n<meta name=\"description\" content=\"Trouvez une organisation de patients atteints d\u2019amylose pr\u00e8s de chez vous. Des organisations membres dans 19 pays, qui accompagnent chacune les patients et les familles de leur pays.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.amyloidosisalliance.org\/fr\/membres\/\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Organisations de patients atteints d\u2019amylose dans le monde\" \/>\n<meta property=\"og:description\" content=\"Trouvez une organisation de patients atteints d\u2019amylose pr\u00e8s de chez vous. 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