{"id":2453,"date":"2026-07-29T15:16:01","date_gmt":"2026-07-29T13:16:01","guid":{"rendered":"https:\/\/www.amyloidosisalliance.org\/miembros-de-la-alianza\/"},"modified":"2026-10-22T15:58:32","modified_gmt":"2026-10-22T13:58:32","slug":"miembros","status":"publish","type":"page","link":"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/","title":{"rendered":"Miembros de la Alianza"},"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=\"\/\">Inicio<\/a><span class=\"aa-breadcrumb__sep\">\u203a<\/span><a href=\"https:\/\/www.amyloidosisalliance.org\/es\/quienes-somos\/\">La Alianza<\/a><span class=\"aa-breadcrumb__sep\">\u203a<\/span><span class=\"aa-breadcrumb__current\">Miembros de la Alianza<\/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\">La Alianza<\/p>\n\n\n\n<h1 class=\"wp-block-heading\">Miembros de la Alianza<\/h1>\n\n\n\n<p class=\"aa-lead wp-block-paragraph\">Asociaciones de todo el mundo. Nuestros miembros son las organizaciones de pacientes que hacen de la Alianza una voz verdaderamente mundial en la lucha contra la amiloidosis.<\/p>\n\n\n\n<p class=\"aa-page-hero__body wp-block-paragraph\">Cada una acompa\u00f1a a los pacientes y las familias de su pa\u00eds y, juntas, comparten conocimientos, recursos y campa\u00f1as m\u00e1s all\u00e1 de las fronteras.<\/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\">D\u00f3nde estamos<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Una red en todo el mundo<\/h2>\n\n\n\n<div class=\"aa-divider-dot\"><\/div>\n\n\n\n<p class=\"wp-block-paragraph\">Cada punto se\u00f1ala un pa\u00eds donde una organizaci\u00f3n miembro lucha contra la amiloidosis. Haga clic en un punto para ver las organizaciones que tienen all\u00ed su 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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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, asociaci\\u00f3n belga de la amiloidosis&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/es\\\/miembros\\\/amybel-asociacion-belga-de-la-amiloidosis\\\/&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, fundaci\\u00f3n neerlandesa de la amiloidosis&quot;,&quot;url&quot;:&quot;https:\\\/\\\/www.amyloidosisalliance.org\\\/es\\\/miembros\\\/amyloidose-nederland-fundacion-neerlandesa-de-la-amiloidosis\\\/&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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\\\/es\\\/miembros\\\/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\">Asociaciones de todo el mundo<\/p>\n\n\t\t\t\n\n<h2 class=\"wp-block-heading\">Los miembros de la Alianza<\/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\">Haga clic en una organizaci\u00f3n para leer su presentaci\u00f3n, visitar su sitio web y encontrar sus cuentas en redes sociales.<\/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-2597 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\/es\/miembros\/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\/es\/miembros\/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\">ABeA es la Asociaci\u00f3n Balear en Amiloidosis, una organizaci\u00f3n sin \u00e1nimo de lucro dedicada a mejorar la calidad de vida de las personas afectadas por la amiloidosis y de sus familias. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/abea-asociacion-balear-en-amiloidosis\/\" target=\"_self\">M\u00e1s informaci\u00f3n<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-2587 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\/es\/miembros\/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\/es\/miembros\/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\">Fundada en 1989, ABPAR (Associa\u00e7\u00e3o Brasileira de Amiloidose) es una organizaci\u00f3n sin \u00e1nimo de lucro dedicada a apoyar a los pacientes y a sus familias mediante la concienciaci\u00f3n, la informaci\u00f3n y la incidencia en&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/abpar-associacao-brasileira-de-amiloidose\/\" target=\"_self\">M\u00e1s informaci\u00f3n<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-2602 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\/es\/miembros\/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\/es\/miembros\/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\">La Association Fran\u00e7aise contre l\u2019Amylose re\u00fane a pacientes, familias y cuidadores afectados por la amiloidosis en Francia. Informa y acompa\u00f1a a los pacientes reci\u00e9n diagnosticados y trabaja junto a los profesionales sanitarios para acortar&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/afca-association-francaise-contre-lamylose\/\" target=\"_self\">M\u00e1s informaci\u00f3n<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-2544 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n de pacientes que trabaja por las personas que viven con amiloidosis y sus familias (Spain), y miembro de la Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/amilo\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: Amilo<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2591 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\/es\/miembros\/amybel-asociacion-belga-de-la-amiloidosis\/\" 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, asociaci\u00f3n belga de la amiloidosis\" 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\/es\/miembros\/amybel-asociacion-belga-de-la-amiloidosis\/\" target=\"_self\" >Amybel, asociaci\u00f3n belga de la amiloidosis<\/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 es una asociaci\u00f3n de pacientes joven pero en r\u00e1pido crecimiento, para las personas con cualquier forma de amiloidosis en B\u00e9lgica. Se centra en ofrecer apoyo e informaci\u00f3n a los pacientes y en dar&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/amybel-asociacion-belga-de-la-amiloidosis\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: Amybel, asociaci\u00f3n belga de la amiloidosis<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2571 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\/es\/miembros\/amyloidose-nederland-fundacion-neerlandesa-de-la-amiloidosis\/\" 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, fundaci\u00f3n neerlandesa de la amiloidosis\" 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\/es\/miembros\/amyloidose-nederland-fundacion-neerlandesa-de-la-amiloidosis\/\" target=\"_self\" >Amylo\u00efdose Nederland, fundaci\u00f3n neerlandesa de la amiloidosis<\/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 Fundaci\u00f3n Neerlandesa de la Amiloidosis (Stichting Amylo\u00efdose Nederland) defiende los intereses de los pacientes con amiloidosis. Para ello, ofrece informaci\u00f3n fiable sobre la enfermedad tanto a pacientes como a profesionales, organiza encuentros para&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/amyloidose-nederland-fundacion-neerlandesa-de-la-amiloidosis\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: Amylo\u00efdose Nederland, fundaci\u00f3n neerlandesa de la amiloidosis<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2560 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n de pacientes que trabaja por las personas que viven con amiloidosis y sus familias (the United States), y miembro de la Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/amyloidosis-support-groups\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: Amyloidosis Support Groups<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2594 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n ben\u00e9fica dirigida por pacientes que conecta a las personas, comparte conocimientos, defiende a las personas afectadas por la amiloidosis y da a conocer la enfermedad en todo el Reino&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/amyloidosis-uk\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: Amyloidosis UK<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2566 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n de pacientes que trabaja por las personas que viven con amiloidosis y sus familias (Spain), y miembro de la Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/asvea\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: ASVEA<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2563 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n de pacientes que trabaja por las personas que viven con amiloidosis y sus familias (Ireland), y miembro de la Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/attr-amyloidosis-all-ireland\/\" target=\"_self\">M\u00e1s informaci\u00f3n<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-2538 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n de pacientes que trabaja por las personas que viven con amiloidosis y sus familias (Australia), y miembro de la Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/australian-amyloidosis-network\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: Australian Amyloidosis Network<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2556 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\/es\/miembros\/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\/es\/miembros\/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. es una organizaci\u00f3n sin \u00e1nimo de lucro, registrada a nivel federal y formada \u00edntegramente por voluntarios, comprometida con mejorar la vida de los pacientes y cuidadores afectados por&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/canadian-amyloidosis-support-network\/\" target=\"_self\">M\u00e1s informaci\u00f3n<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-2605 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\/es\/miembros\/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\/es\/miembros\/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 apoya a los pacientes y familias que viven con amiloidosis hereditaria por transtiretina en el norte de Suecia, donde la enfermedad tiene una presencia especialmente alta. La asociaci\u00f3n organiza encuentros entre pacientes&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/famy-norrbotten\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: FaMY Norrbotten<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2547 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n de pacientes que trabaja por las personas que viven con amiloidosis y sus familias (Italy), y miembro de la Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/famy-associazione-italiana-amiloidosi-familiare-onlus\/\" target=\"_self\">M\u00e1s informaci\u00f3n<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-2550 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n de pacientes que trabaja por las personas que viven con amiloidosis y sus familias (Germany), y miembro de la Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/fap-ev\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: FAP-eV<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2568 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n de pacientes que trabaja por las personas que viven con amiloidosis y sus familias (Mexico), y miembro de la Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/ffam\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: FFAM<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2577 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\/es\/miembros\/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\/es\/miembros\/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) es una fundaci\u00f3n sin \u00e1nimo de lucro dedicada a mejorar la calidad de vida y la esperanza de vida de las personas y familias afectadas por enfermedades&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/funcolehf-fundacion-colombiana-para-enfermedades-huerfanas\/\" target=\"_self\">M\u00e1s informaci\u00f3n<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-2541 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n de pacientes que trabaja por las personas que viven con amiloidosis y sus familias (South Korea), y miembro de la Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/hereditary-amyloidosis-hwanwoohoe\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: Hereditary Amyloidosis Hwanwoohoe<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2574 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\/es\/miembros\/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\/es\/miembros\/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\">La Israel Amyloidosis Association fue fundada en 2016 por un grupo de pacientes con amiloidosis AL, movidos por un esp\u00edritu de colaboraci\u00f3n y responsabilidad y por la convicci\u00f3n de que los pacientes y sus&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/israel-amyloidosis-association\/\" target=\"_self\">M\u00e1s informaci\u00f3n<span class=\"screen-reader-text\">: Israel Amyloidosis Association<\/span><\/a>\n\t\t\t<\/div>\n\n<\/li><li class=\"wp-block-post post-2584 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n nacional dirigida por pacientes que apoya a las personas que viven con amiloidosis y a sus familias. Fundada en 2019, se compromete a dar a&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/leben-mit-amyloidose-amyloidosis-austria\/\" target=\"_self\">M\u00e1s informaci\u00f3n<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-2580 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\/es\/miembros\/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\/es\/miembros\/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) es una organizaci\u00f3n sin \u00e1nimo de lucro dedicada a mejorar la vida de las personas afectadas por todas las formas de amiloidosis mediante la concienciaci\u00f3n, la informaci\u00f3n,&hellip; <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/nzapa-new-zealand-amyloidosis-patient-association\/\" target=\"_self\">M\u00e1s informaci\u00f3n<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-2553 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\/es\/miembros\/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\/es\/miembros\/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 es una organizaci\u00f3n de pacientes que trabaja por las personas que viven con amiloidosis y sus familias (Canada), y miembro de la Amyloidosis Alliance. <\/p><\/div>\n\t\t\t\t\n<a class=\"aa-member-card__more wp-block-read-more\" href=\"https:\/\/www.amyloidosisalliance.org\/es\/miembros\/ttr-amyloidosis-canada\/\" target=\"_self\">M\u00e1s informaci\u00f3n<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\">Nuestros miembros son las asociaciones nacionales de pacientes que forman la red. Se distinguen de nuestros colaboradores, las empresas e instituciones que apoyan el trabajo de la Alianza.<\/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\">Hacerse miembro<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">\u00bfSu organizaci\u00f3n no figura en esta lista?<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">Las organizaciones de pacientes que luchan contra la amiloidosis, en cualquier parte del mundo, est\u00e1n invitadas a presentar su candidatura. Las organizaciones creadas hace menos de un a\u00f1o se unen a la Alianza como miembros asociados, mientras se consolidan.<\/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\">Solicite unirse a la Alianza<\/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\">C\u00f3mo funciona<\/h3>\n\n\n\n<ul class=\"wp-block-list aa-checklist__items\">\n<li>Env\u00edenos una breve solicitud mediante el formulario que aparece a continuaci\u00f3n.<\/li>\n\n\n\n<li>Organizamos una conversaci\u00f3n con una persona de la Alianza, para conocer su organizaci\u00f3n, sus proyectos y su situaci\u00f3n actual.<\/li>\n\n\n\n<li>Despu\u00e9s le pedimos una breve presentaci\u00f3n de su organizaci\u00f3n (de 3 a 4 l\u00edneas), la direcci\u00f3n de su sitio web, los enlaces a sus cuentas en redes sociales, un folleto de presentaci\u00f3n en formato PDF si dispone de uno, y su logotipo en formato PNG de alta calidad, preferiblemente con fondo transparente.<\/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\">Solicitud de adhesi\u00f3n<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Solicite unirse a la Alianza<\/h2>\n\n\n\n<div class=\"aa-divider-dot\"><\/div>\n\n\n\n<p class=\"wp-block-paragraph\">Pres\u00e9ntenos su organizaci\u00f3n. Una persona de la Alianza se pondr\u00e1 en contacto con usted para organizar una conversaci\u00f3n.<\/p>\n<\/div>\n\n\n\n<div class=\"wpcf7 no-js\" id=\"wpcf7-f2507-o1\" lang=\"es-ES\" dir=\"ltr\" data-wpcf7-id=\"2507\">\n<div class=\"screen-reader-response\"><p role=\"status\" aria-live=\"polite\" aria-atomic=\"true\"><\/p> <ul><\/ul><\/div>\n<form action=\"\/es\/wp-json\/wp\/v2\/pages\/2453#wpcf7-f2507-o1\" method=\"post\" class=\"wpcf7-form init\" aria-label=\"Formulario de contacto\" novalidate=\"novalidate\" data-status=\"init\">\n<fieldset class=\"hidden-fields-container\"><input type=\"hidden\" name=\"_wpcf7\" value=\"2507\" \/><input type=\"hidden\" name=\"_wpcf7_version\" value=\"6.1.7\" \/><input type=\"hidden\" name=\"_wpcf7_locale\" value=\"es_ES\" \/><input type=\"hidden\" name=\"_wpcf7_unit_tag\" value=\"wpcf7-f2507-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\">Su nombre <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\">Su correo electr\u00f3nico <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\">Su organizaci\u00f3n <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\">Pa\u00eds <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\">El sitio web de su organizaci\u00f3n<\/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\">Pres\u00e9ntenos su organizaci\u00f3n<\/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\">Acepto que la informaci\u00f3n enviada a trav\u00e9s de este formulario sea utilizada por la Amyloidosis Alliance para tramitar mi solicitud. Nunca se ceder\u00e1 a terceros.<\/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=\"Enviar su 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\">Ir m\u00e1s all\u00e1<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">La Alianza<\/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\/es\/quienes-somos\/\">Sobre nosotros<\/a><\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Qui\u00e9nes somos, c\u00f3mo naci\u00f3 la Alianza y qu\u00e9 une a nuestros miembros.<\/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\/es\/nuestros-colaboradores\/\">Nuestros colaboradores<\/a><\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Las empresas e instituciones cuyo apoyo nos ayuda a llevar a cabo nuestros proyectos en todo el mundo.<\/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\/es\/unase-a-nosotros\/\">\u00danase a nosotros<\/a><\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Incorpore su asociaci\u00f3n a la red y luche contra la amiloidosis a nuestro lado.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/section>\n","protected":false},"excerpt":{"rendered":"<p>Inicio\u203aLa Alianza\u203aMiembros de la Alianza La Alianza Miembros de la Alianza Asociaciones de todo el mundo. Nuestros miembros son las organizaciones de pacientes que hacen de la Alianza una voz verdaderamente mundial en la lucha contra la amiloidosis. Cada una acompa\u00f1a a los pacientes y las familias de su pa\u00eds y, juntas, comparten conocimientos, recursos [&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-2453","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>Organizaciones de pacientes con amiloidosis en todo el mundo<\/title>\n<meta name=\"description\" content=\"Encuentre una organizaci\u00f3n de pacientes con amiloidosis cerca de usted. 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