{"id":2791,"date":"2026-07-29T15:16:01","date_gmt":"2026-07-29T13:16:01","guid":{"rendered":"https:\/\/www.amyloidosisalliance.org\/membri-dellalleanza\/"},"modified":"2026-11-02T11:57:25","modified_gmt":"2026-11-02T10:57:25","slug":"membri","status":"publish","type":"page","link":"https:\/\/www.amyloidosisalliance.org\/it\/membri\/","title":{"rendered":"Membri dell\u2019Alleanza"},"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=\"\/\">Home<\/a><span class=\"aa-breadcrumb__sep\">\u203a<\/span><a href=\"https:\/\/www.amyloidosisalliance.org\/it\/chi-siamo\/\">L\u2019Alleanza<\/a><span class=\"aa-breadcrumb__sep\">\u203a<\/span><span class=\"aa-breadcrumb__current\">Membri dell\u2019Alleanza<\/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\u2019Alleanza<\/p>\n\n\n\n<h1 class=\"wp-block-heading\">Membri dell\u2019Alleanza<\/h1>\n\n\n\n<p class=\"aa-lead wp-block-paragraph\">Associazioni da tutto il mondo. I nostri membri sono le organizzazioni di pazienti che fanno dell\u2019Alleanza una voce davvero mondiale nella lotta contro l\u2019amiloidosi.<\/p>\n\n\n\n<p class=\"aa-page-hero__body wp-block-paragraph\">Ognuna sostiene i pazienti e le famiglie del proprio paese e, insieme, condividono conoscenze, risorse e campagne al di l\u00e0 dei confini.<\/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\">Dove siamo<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Una rete in tutto il mondo<\/h2>\n\n\n\n<div class=\"aa-divider-dot\"><\/div>\n\n\n\n<p class=\"wp-block-paragraph\">Ogni punto indica un paese in cui un\u2019associazione membro lotta contro l\u2019amiloidosi. Cliccate su un punto per visualizzare le organizzazioni che vi hanno sede.<\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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, associazione belga per l\\u2019amiloidosi&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/it\\\/membri\\\/amybel-associazione-belga-per-lamiloidosi\\\/&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, fondazione olandese per l\\u2019amiloidosi&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/it\\\/membri\\\/amyloidose-nederland-fondazione-olandese-per-lamiloidosi\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/Publication-type-e1786715454575-150x150.png&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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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\\\/it\\\/membri\\\/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;Austria&quot;,&quot;lat&quot;:48.21,&quot;lng&quot;:16.37,&quot;members&quot;:[{&quot;title&quot;:&quot;Leben mit Amyloidose \\u2013 Amyloidosis Austria&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/it\\\/membri\\\/leben-mit-amyloidose-amyloidosis-austria\\\/&quot;,&quot;logo&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/08\\\/Logo_LMA-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\\\/it\\\/membri\\\/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\">Associazioni da tutto il mondo<\/p>\n\n\t\t\t\n\n<h2 class=\"wp-block-heading\">I membri dell\u2019Alleanza<\/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\">Cliccate su un\u2019organizzazione per leggerne la presentazione, visitarne il sito web e trovarne i profili sui social network.<\/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-2967 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\/it\/membri\/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\/it\/membri\/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 \u00e8 l\u2019associazione per l\u2019amiloidosi delle Isole Baleari, un\u2019organizzazione senza scopo di lucro che si impegna a migliorare la qualit\u00e0 di vita delle persone colpite dall\u2019amiloidosi e delle loro famiglie. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/abea-asociacion-balear-en-amiloidosis\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: ABeA, Asociaci\u00f3n Balear en Amiloidosis<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2957 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\/it\/membri\/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\/it\/membri\/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\">Fondata nel 1989, l\u2019ABPAR (Associa\u00e7\u00e3o Brasileira de Amiloidose) \u00e8 un\u2019organizzazione senza scopo di lucro che sostiene i pazienti e le famiglie promuovendo la sensibilizzazione, l\u2019informazione e l\u2019advocacy sull\u2019amiloidosi. Animata da volontari, pazienti e caregiver,&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/abpar-associacao-brasileira-de-amiloidose\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: ABPAR, Associa\u00e7\u00e3o Brasileira de Amiloidose<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2972 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\/it\/membri\/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\/it\/membri\/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 riunisce pazienti, famiglie e caregiver colpiti dall\u2019amiloidosi in Francia. Informa e accompagna i pazienti che hanno appena ricevuto la diagnosi e lavora al fianco dei professionisti sanitari per accorciare il&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/afca-association-francaise-contre-lamylose\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: AFCA, Association Fran\u00e7aise contre l\u2019Amylose<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2914 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\/it\/membri\/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\/it\/membri\/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 \u00e8 un\u2019organizzazione di pazienti che si impegna per le persone che vivono con l\u2019amiloidosi e per le loro famiglie (Spain), e membro dell\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\/it\/membri\/amilo\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: Amilo<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2961 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\/it\/membri\/amybel-associazione-belga-per-lamiloidosi\/\" 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, associazione belga per l\u2019amiloidosi\" 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\/it\/membri\/amybel-associazione-belga-per-lamiloidosi\/\" target=\"_self\" >Amybel, associazione belga per l\u2019amiloidosi<\/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 \u00e8 un\u2019associazione di pazienti giovane ma in rapida crescita, per le persone con qualsiasi forma di amiloidosi in Belgio. Si dedica a offrire sostegno e informazioni ai pazienti e a fare conoscere l\u2019amiloidosi&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/amybel-associazione-belga-per-lamiloidosi\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: Amybel, associazione belga per l\u2019amiloidosi<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2941 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\/it\/membri\/amyloidose-nederland-fondazione-olandese-per-lamiloidosi\/\" 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, fondazione olandese per l\u2019amiloidosi\" 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\/it\/membri\/amyloidose-nederland-fondazione-olandese-per-lamiloidosi\/\" target=\"_self\" >Amylo\u00efdose Nederland, fondazione olandese per l\u2019amiloidosi<\/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 Fondazione olandese per l\u2019amiloidosi (Stichting Amylo\u00efdose Nederland) tutela gli interessi dei pazienti affetti da amiloidosi. Lo fa fornendo informazioni affidabili sulla malattia sia ai pazienti sia ai professionisti, organizzando incontri per i pazienti&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/amyloidose-nederland-fondazione-olandese-per-lamiloidosi\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: Amylo\u00efdose Nederland, fondazione olandese per l\u2019amiloidosi<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2930 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\/it\/membri\/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\/it\/membri\/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 \u00e8 un\u2019organizzazione di pazienti che si impegna per le persone che vivono con l\u2019amiloidosi e per le loro famiglie (the United States), e membro dell\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\/it\/membri\/amyloidosis-support-groups\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: Amyloidosis Support Groups<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2964 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\/it\/membri\/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\/it\/membri\/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 \u00e8 un\u2019associazione benefica guidata da pazienti che mette in contatto le persone, condivide conoscenze, difende chi \u00e8 colpito dall\u2019amiloidosi e fa conoscere la malattia in tutto il Regno Unito. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/amyloidosis-uk\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: Amyloidosis UK<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2936 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\/it\/membri\/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\/it\/membri\/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 \u00e8 un\u2019organizzazione di pazienti che si impegna per le persone che vivono con l\u2019amiloidosi e per le loro famiglie (Spain), e membro dell\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\/it\/membri\/asvea\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: ASVEA<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2933 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\/it\/membri\/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\/it\/membri\/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 \u00e8 un\u2019organizzazione di pazienti che si impegna per le persone che vivono con l\u2019amiloidosi e per le loro famiglie (Ireland), e membro dell\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\/it\/membri\/attr-amyloidosis-all-ireland\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: ATTR Amyloidosis All Ireland<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2908 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\/it\/membri\/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\/it\/membri\/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 \u00e8 un\u2019organizzazione di pazienti che si impegna per le persone che vivono con l\u2019amiloidosi e per le loro famiglie (Australia), e membro dell\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\/it\/membri\/australian-amyloidosis-network\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: Australian Amyloidosis Network<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2926 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\/it\/membri\/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\/it\/membri\/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\">La Canadian Amyloidosis Support Network, Inc. \u00e8 un\u2019organizzazione senza scopo di lucro, registrata a livello federale e composta interamente da volontari, impegnata a migliorare concretamente la vita dei pazienti e dei caregiver colpiti dall\u2019amiloidosi&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/canadian-amyloidosis-support-network\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: Canadian Amyloidosis Support Network<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2975 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\/it\/membri\/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\/it\/membri\/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 sostiene i pazienti e le famiglie che convivono con l\u2019amiloidosi ereditaria da transtiretina nel nord della Svezia, dove la malattia \u00e8 particolarmente diffusa. L\u2019associazione organizza incontri tra pazienti e diffonde nella propria&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/famy-norrbotten\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: FaMY Norrbotten<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2917 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\/it\/membri\/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\/it\/membri\/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 \u00e8 un\u2019organizzazione di pazienti che si impegna per le persone che vivono con l\u2019amiloidosi e per le loro famiglie (Italy), e membro dell\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\/it\/membri\/famy-associazione-italiana-amiloidosi-familiare-onlus\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: FAMY, Associazione Italiana Amiloidosi Familiare Onlus<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2920 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\/it\/membri\/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\/it\/membri\/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 \u00e8 un\u2019organizzazione di pazienti che si impegna per le persone che vivono con l\u2019amiloidosi e per le loro famiglie (Germany), e membro dell\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\/it\/membri\/fap-ev\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: FAP-eV<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2938 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\/it\/membri\/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\/it\/membri\/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 \u00e8 un\u2019organizzazione di pazienti che si impegna per le persone che vivono con l\u2019amiloidosi e per le loro famiglie (Mexico), e membro dell\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\/it\/membri\/ffam\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: FFAM<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2947 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\/it\/membri\/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\/it\/membri\/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) \u00e8 una fondazione senza scopo di lucro che si impegna a migliorare la qualit\u00e0 e l\u2019aspettativa di vita delle persone e delle famiglie colpite da malattie rare,&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/funcolehf-fundacion-colombiana-para-enfermedades-huerfanas\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: FUNCOLEHF, Fundaci\u00f3n Colombiana para Enfermedades Hu\u00e9rfanas<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2911 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\/it\/membri\/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\/it\/membri\/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 \u00e8 un\u2019organizzazione di pazienti che si impegna per le persone che vivono con l\u2019amiloidosi e per le loro famiglie (South Korea), e membro dell\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\/it\/membri\/hereditary-amyloidosis-hwanwoohoe\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: Hereditary Amyloidosis Hwanwoohoe<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2944 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\/it\/membri\/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\/it\/membri\/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 \u00e8 stata fondata nel 2016 da un gruppo di pazienti affetti da amiloidosi AL, per spirito di collaborazione e di responsabilit\u00e0 e nella convinzione che i pazienti e le loro famiglie&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/israel-amyloidosis-association\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: Israel Amyloidosis Association<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2954 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\/it\/membri\/leben-mit-amyloidose-amyloidosis-austria\/\" 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=\"Leben mit Amyloidose \u2013 Amyloidosis Austria\" 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\/it\/membri\/leben-mit-amyloidose-amyloidosis-austria\/\" target=\"_self\" >Leben mit Amyloidose \u2013 Amyloidosis Austria<\/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 \u00e8 un\u2019organizzazione nazionale guidata da pazienti che sostiene le persone che convivono con l\u2019amiloidosi e le loro famiglie. Fondata nel 2019, si impegna a fare conoscere la malattia,&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/leben-mit-amyloidose-amyloidosis-austria\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: Leben mit Amyloidose \u2013 Amyloidosis Austria<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2950 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\/it\/membri\/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\/it\/membri\/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) \u00e8 un\u2019organizzazione senza scopo di lucro che si impegna a migliorare la vita delle persone colpite da tutte le forme di amiloidosi attraverso la sensibilizzazione, l\u2019informazione, l\u2019advocacy&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/it\/membri\/nzapa-new-zealand-amyloidosis-patient-association\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: NZAPA, New Zealand Amyloidosis Patient Association<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2923 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\/it\/membri\/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\/it\/membri\/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 \u00e8 un\u2019organizzazione di pazienti che si impegna per le persone che vivono con l\u2019amiloidosi e per le loro famiglie (Canada), e membro dell\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\/it\/membri\/ttr-amyloidosis-canada\/\" target=\"_self\">Per saperne di pi\u00f9<span class=\"screen-reader-text\">: 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\">I nostri membri sono le associazioni nazionali di pazienti che compongono la rete. Si distinguono dai nostri partner, le aziende e le istituzioni che sostengono il lavoro dell\u2019Alleanza.<\/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\">Diventare membro<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">La vostra organizzazione non compare in questo elenco?<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">Le organizzazioni di pazienti che lottano contro l\u2019amiloidosi, in qualsiasi parte del mondo, sono invitate a presentare la propria candidatura. Le organizzazioni nate da meno di un anno entrano nell\u2019Alleanza come membri associati, il tempo di consolidarsi.<\/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\">Chiedete di aderire all\u2019Alleanza<\/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\">Come funziona<\/h3>\n\n\n\n<ul class=\"wp-block-list aa-checklist__items\">\n<li>Inviateci una breve richiesta tramite il modulo qui sotto.<\/li>\n\n\n\n<li>Organizziamo un colloquio con una persona dell\u2019Alleanza, per conoscere la vostra organizzazione, i vostri progetti e la vostra situazione attuale.<\/li>\n\n\n\n<li>Vi chiediamo poi una breve presentazione della vostra organizzazione (3-4 righe), l\u2019indirizzo del vostro sito web, i link ai vostri profili sui social network, una brochure di presentazione in formato PDF se disponibile, e il vostro logo in formato PNG ad alta qualit\u00e0, preferibilmente su sfondo trasparente.<\/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\">Domanda di adesione<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Chiedete di aderire all\u2019Alleanza<\/h2>\n\n\n\n<div class=\"aa-divider-dot\"><\/div>\n\n\n\n<p class=\"wp-block-paragraph\">Presentateci la vostra organizzazione. Una persona dell\u2019Alleanza vi ricontatter\u00e0 per organizzare un colloquio.<\/p>\n<\/div>\n\n\n\n<div class=\"wpcf7 no-js\" id=\"wpcf7-f2870-o1\" lang=\"it-IT\" dir=\"ltr\" data-wpcf7-id=\"2870\">\n<div class=\"screen-reader-response\"><p role=\"status\" aria-live=\"polite\" aria-atomic=\"true\"><\/p> <ul><\/ul><\/div>\n<form action=\"\/it\/wp-json\/wp\/v2\/pages\/2791#wpcf7-f2870-o1\" method=\"post\" class=\"wpcf7-form init\" aria-label=\"Modulo di contatto\" novalidate=\"novalidate\" data-status=\"init\">\n<fieldset class=\"hidden-fields-container\"><input type=\"hidden\" name=\"_wpcf7\" value=\"2870\" \/><input type=\"hidden\" name=\"_wpcf7_version\" value=\"6.1.7\" \/><input type=\"hidden\" name=\"_wpcf7_locale\" value=\"it_IT\" \/><input type=\"hidden\" name=\"_wpcf7_unit_tag\" value=\"wpcf7-f2870-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\">Il vostro nome <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\">Il vostro indirizzo 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\">La vostra organizzazione <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\">Paese <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\">Il sito web della vostra organizzazione<\/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\">Presentateci la vostra organizzazione<\/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\">Accetto che le informazioni inviate tramite questo modulo siano utilizzate dall\u2019Amyloidosis Alliance per gestire la mia richiesta. Non saranno mai comunicate a terzi.<\/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=\"Inviate la vostra candidatura\" \/>\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\">Per saperne di pi\u00f9<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">L\u2019Alleanza<\/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\/it\/chi-siamo\/\">Chi siamo<\/a><\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Chi siamo, come \u00e8 nata l\u2019Alleanza e cosa unisce i nostri membri.<\/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\/it\/i-nostri-partner\/\">I nostri partner<\/a><\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Le aziende e le istituzioni il cui sostegno ci aiuta a portare avanti i nostri progetti in tutto il mondo.<\/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\/it\/unitevi-a-noi\/\">Unitevi a noi<\/a><\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Fate entrare la vostra associazione nella rete e lottate contro l\u2019amiloidosi al nostro fianco.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/section>\n","protected":false},"excerpt":{"rendered":"<p>Home\u203aL\u2019Alleanza\u203aMembri dell\u2019Alleanza L\u2019Alleanza Membri dell\u2019Alleanza Associazioni da tutto il mondo. I nostri membri sono le organizzazioni di pazienti che fanno dell\u2019Alleanza una voce davvero mondiale nella lotta contro l\u2019amiloidosi. Ognuna sostiene i pazienti e le famiglie del proprio paese e, insieme, condividono conoscenze, risorse e campagne al di l\u00e0 dei confini. Dove siamo Una rete [&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-2791","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>Organizzazioni di pazienti con amiloidosi nel mondo<\/title>\n<meta name=\"description\" content=\"Trovate un\u2019organizzazione di pazienti con amiloidosi vicino a voi. 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