{"id":4736,"date":"2023-06-06T07:41:00","date_gmt":"2023-06-06T05:41:00","guid":{"rendered":"https:\/\/www.amyloidosisalliance.org\/het-whf-forum-in-zwitserland\/"},"modified":"2026-11-03T10:32:48","modified_gmt":"2026-11-03T09:32:48","slug":"het-whf-forum-in-zwitserland","status":"publish","type":"post","link":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/","title":{"rendered":"Het WHF-forum in Zwitserland"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">De World Heart Federation (WHF) organiseerde op 17 en 18 mei 2023 in Gen\u00e8ve (Zwitserland) een speciaal forum met de titel \u201cSHINING A LIGHT ON RARE CARDIOVASCULAR DISEASES\u201d (zeldzame hart- en vaatziekten in de schijnwerpers), voorafgaand aan de World Heart Summit 2023 van 19 tot 21 mei. Pati\u00ebntvertegenwoordigers met eigen ervaring met vier zeldzame hart- en vaatziekten werden uitgenodigd om het perspectief van pati\u00ebnten in te brengen en mee vorm te geven aan de strategie\u00ebn van de WHF voor de diagnose en behandeling van deze zeldzame hart- en vaatziekten:<\/p>\n\n<h2 class=\"wp-block-heading\">Het panel bestond uit pati\u00ebntvertegenwoordigers voor de volgende vier zeldzame hart- en vaatziekten:\u00a0<\/h2>\n\n<div class=\"wp-block-group is-vertical is-layout-flex wp-container-core-group-is-layout-1bbac977 wp-block-group-is-layout-flex\">\n<ul class=\"wp-block-list\">\n<li>pulmonale arteri\u00eble hypertensie (PAH),\u00a0<\/li>\n\n\n\n<li>homozygote familiaire hypercholesterolemie (HoFH)\u00a0<\/li>\n\n\n\n<li>transthyretine-amylo\u00efde cardiomyopathie (ATTR-CM)\u00a0<\/li>\n\n\n\n<li>erfelijke hypertrofische cardiomyopathie\u00a0<\/li>\n<\/ul>\n<\/div>\n\n<p class=\"wp-block-paragraph\">Het forum werd geopend door dr. Daniel Pi\u00f1eiro, voorzitter van de WHF, die ons eraan herinnerde dat: \u00a0<\/p>\n\n<ul class=\"wp-block-list\">\n<li>Gezondheid een mensenrecht is, en alle pati\u00ebnten een langer leven en een betere levenskwaliteit verdienen.<\/li>\n\n\n\n<li>De stem van pati\u00ebnten zelf meer waard is dan artsen die namens pati\u00ebnten spreken.\u00a0<\/li>\n<\/ul>\n\n<p class=\"wp-block-paragraph\">Gespecialiseerde artsen voor elk van de vier zeldzame ziekten gaven een presentatie aan de groep. Dr. Nikki Bart, van de University of New South Wales (Australi\u00eb), nam op afstand deel aan het forum om de belangrijkste uitdagingen voor pati\u00ebnten met ATTR-CM te bespreken. Zij belichtte verschillende kernpunten in de diagnose en behandeling van ATTR-CM, waaronder vertraging in de diagnose en in de toegang tot behandeling.\u00a0<\/p>\n\n<p class=\"wp-block-paragraph\">Keith Dares uit Canada, lid van de Amyloidosis Alliance, is een pati\u00ebnt met ATTR-CM. Keith nam graag deel aan het forum om te vertellen over zijn weg naar de diagnose en over de invloed van ATTR-CM op zijn dagelijkse activiteiten. De workshops leidden tot veel groepsdiscussie, waarin verbeterpunten werden vastgesteld:\u00a0<\/p>\n\n<h2 class=\"wp-block-heading\">Wat is er nodig om de weg naar een juiste diagnose te verkorten?\u00a0<\/h2>\n\n<p class=\"wp-block-paragraph\">Hoe kunnen huisartsen beter worden toegerust om gemiste of onjuiste diagnoses te voorkomen: kunnen we aanmoedigen om amylo\u00efdose eerder, en niet later, in de diagnostische protocollen \u201cuit te sluiten\u201d? Kunnen we een hulpmiddel ontwikkelen dat alarmsignalen markeert, voor een vroegere diagnose?\u00a0<\/p>\n\n<div class=\"wp-block-group is-vertical is-layout-flex wp-container-core-group-is-layout-1bbac977 wp-block-group-is-layout-flex\">\n<p class=\"wp-block-paragraph\">Hoe pakken we de ongelijkheid in diagnose bij vrouwelijke pati\u00ebnten aan?<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Welke modellen bestaan er voor \u201cexpertisecentra\u201d? Hoe kunnen we een betere toegang tot betere zorg bereiken?\u00a0<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Hoe verminderen we de drempels om de toegang tot behandelingen te vergroten?\u00a0<\/p>\n<\/div>\n\n<p class=\"wp-block-paragraph\">Bij de presentatie van de eindverslagen op de tweede dag was het interessant om te zien met welke gemeenschappelijke uitdagingen de vier pati\u00ebntengemeenschappen te maken hebben. Interessant was ook het potentieel, dat momenteel wordt onderzocht, van artifici\u00eble intelligentie en \u201cmachine learning\u201d om de tijd tot diagnose te helpen verkorten. <\/p>\n\n<p class=\"wp-block-paragraph\">De World Heart Federation wil de informatie die de pati\u00ebnten hebben gedeeld gebruiken om een werkplan op te stellen dat de uitdagingen aanpakt in de diagnose, behandeling en zorg van mensen met zeldzame hart- en vaatziekten.<\/p>\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2023\/06\/10.png\" alt=\"\" class=\"wp-image-6805\"\/><\/figure>\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" src=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2023\/06\/11.png\" alt=\"\" class=\"wp-image-6806\"\/><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>Op een forum van de World Heart Federation in Gen\u00e8ve in mei 2023 namen pati\u00ebntvertegenwoordigers, onder meer voor ATTR-cardiomyopathie, het woord over zeldzame hartziekten.<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[107],"tags":[],"class_list":["post-4736","post","type-post","status-publish","format-standard","hentry","category-uncategorized-nl"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Het WHF-forum in Zwitserland<\/title>\n<meta name=\"description\" content=\"Op een forum van de World Heart Federation in Gen\u00e8ve in mei 2023 namen pati\u00ebntvertegenwoordigers, onder meer voor ATTR-cardiomyopathie, het woord over zeldzame hartziekten.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/\" \/>\n<meta property=\"og:locale\" content=\"nl_NL\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Het WHF-forum in Zwitserland\" \/>\n<meta property=\"og:description\" content=\"Op een forum van de World Heart Federation in Gen\u00e8ve in mei 2023 namen pati\u00ebntvertegenwoordigers, onder meer voor ATTR-cardiomyopathie, het woord over zeldzame hartziekten.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/\" \/>\n<meta property=\"og:site_name\" content=\"Amyloidosis Alliance\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/AmyloidosisAlliance\/\" \/>\n<meta property=\"article:published_time\" content=\"2023-06-06T05:41:00+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2026-11-03T09:32:48+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/09\/amyloidosisalliance.png\" \/>\n\t<meta property=\"og:image:width\" content=\"1200\" \/>\n\t<meta property=\"og:image:height\" content=\"675\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@amyloidosisa\" \/>\n<meta name=\"twitter:site\" content=\"@amyloidosisa\" \/>\n<meta name=\"twitter:label1\" content=\"Geschatte leestijd\" \/>\n\t<meta name=\"twitter:data1\" content=\"2 minuten\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/\"},\"author\":{\"name\":\"Amyloidosis Alliance\",\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/#organization\"},\"headline\":\"Het WHF-forum in Zwitserland\",\"datePublished\":\"2023-06-06T05:41:00+00:00\",\"dateModified\":\"2026-11-03T09:32:48+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/\"},\"wordCount\":471,\"commentCount\":0,\"publisher\":{\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/#organization\"},\"image\":{\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2023\\\/06\\\/10.png\",\"inLanguage\":\"nl-NL\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/\",\"url\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/\",\"name\":\"Het WHF-forum in Zwitserland\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/#primaryimage\"},\"image\":{\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2023\\\/06\\\/10.png\",\"datePublished\":\"2023-06-06T05:41:00+00:00\",\"dateModified\":\"2026-11-03T09:32:48+00:00\",\"description\":\"Op een forum van de World Heart Federation in Gen\u00e8ve in mei 2023 namen pati\u00ebntvertegenwoordigers, onder meer voor ATTR-cardiomyopathie, het woord over zeldzame hartziekten.\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/#breadcrumb\"},\"inLanguage\":\"nl-NL\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"nl-NL\",\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/#primaryimage\",\"url\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2023\\\/06\\\/10.png\",\"contentUrl\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2023\\\/06\\\/10.png\"},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/het-whf-forum-in-zwitserland\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/home\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Het WHF-forum in Zwitserland\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/#website\",\"url\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/\",\"name\":\"Amyloidosis Alliance\",\"description\":\"\",\"publisher\":{\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"nl-NL\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/#organization\",\"name\":\"Amyloidosis Alliance\",\"url\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"nl-NL\",\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/09\\\/logo.png\",\"contentUrl\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/wp-content\\\/uploads\\\/2026\\\/09\\\/logo.png\",\"width\":252,\"height\":252,\"caption\":\"Amyloidosis Alliance\"},\"image\":{\"@id\":\"https:\\\/\\\/www.amyloidosisalliance.org\\\/nl\\\/#\\\/schema\\\/logo\\\/image\\\/\"},\"sameAs\":[\"https:\\\/\\\/www.facebook.com\\\/AmyloidosisAlliance\\\/\",\"https:\\\/\\\/x.com\\\/amyloidosisa\"]}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Het WHF-forum in Zwitserland","description":"Op een forum van de World Heart Federation in Gen\u00e8ve in mei 2023 namen pati\u00ebntvertegenwoordigers, onder meer voor ATTR-cardiomyopathie, het woord over zeldzame hartziekten.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/","og_locale":"nl_NL","og_type":"article","og_title":"Het WHF-forum in Zwitserland","og_description":"Op een forum van de World Heart Federation in Gen\u00e8ve in mei 2023 namen pati\u00ebntvertegenwoordigers, onder meer voor ATTR-cardiomyopathie, het woord over zeldzame hartziekten.","og_url":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/","og_site_name":"Amyloidosis Alliance","article_publisher":"https:\/\/www.facebook.com\/AmyloidosisAlliance\/","article_published_time":"2023-06-06T05:41:00+00:00","article_modified_time":"2026-11-03T09:32:48+00:00","og_image":[{"width":1200,"height":675,"url":"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/09\/amyloidosisalliance.png","type":"image\/png"}],"twitter_card":"summary_large_image","twitter_creator":"@amyloidosisa","twitter_site":"@amyloidosisa","twitter_misc":{"Geschatte leestijd":"2 minuten"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/#article","isPartOf":{"@id":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/"},"author":{"name":"Amyloidosis Alliance","@id":"https:\/\/www.amyloidosisalliance.org\/nl\/#organization"},"headline":"Het WHF-forum in Zwitserland","datePublished":"2023-06-06T05:41:00+00:00","dateModified":"2026-11-03T09:32:48+00:00","mainEntityOfPage":{"@id":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/"},"wordCount":471,"commentCount":0,"publisher":{"@id":"https:\/\/www.amyloidosisalliance.org\/nl\/#organization"},"image":{"@id":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/#primaryimage"},"thumbnailUrl":"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2023\/06\/10.png","inLanguage":"nl-NL"},{"@type":"WebPage","@id":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/","url":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/","name":"Het WHF-forum in Zwitserland","isPartOf":{"@id":"https:\/\/www.amyloidosisalliance.org\/nl\/#website"},"primaryImageOfPage":{"@id":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/#primaryimage"},"image":{"@id":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/#primaryimage"},"thumbnailUrl":"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2023\/06\/10.png","datePublished":"2023-06-06T05:41:00+00:00","dateModified":"2026-11-03T09:32:48+00:00","description":"Op een forum van de World Heart Federation in Gen\u00e8ve in mei 2023 namen pati\u00ebntvertegenwoordigers, onder meer voor ATTR-cardiomyopathie, het woord over zeldzame hartziekten.","breadcrumb":{"@id":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/#breadcrumb"},"inLanguage":"nl-NL","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/"]}]},{"@type":"ImageObject","inLanguage":"nl-NL","@id":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/#primaryimage","url":"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2023\/06\/10.png","contentUrl":"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2023\/06\/10.png"},{"@type":"BreadcrumbList","@id":"https:\/\/www.amyloidosisalliance.org\/nl\/het-whf-forum-in-zwitserland\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.amyloidosisalliance.org\/nl\/home\/"},{"@type":"ListItem","position":2,"name":"Het WHF-forum in Zwitserland"}]},{"@type":"WebSite","@id":"https:\/\/www.amyloidosisalliance.org\/nl\/#website","url":"https:\/\/www.amyloidosisalliance.org\/nl\/","name":"Amyloidosis Alliance","description":"","publisher":{"@id":"https:\/\/www.amyloidosisalliance.org\/nl\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.amyloidosisalliance.org\/nl\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"nl-NL"},{"@type":"Organization","@id":"https:\/\/www.amyloidosisalliance.org\/nl\/#organization","name":"Amyloidosis Alliance","url":"https:\/\/www.amyloidosisalliance.org\/nl\/","logo":{"@type":"ImageObject","inLanguage":"nl-NL","@id":"https:\/\/www.amyloidosisalliance.org\/nl\/#\/schema\/logo\/image\/","url":"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/09\/logo.png","contentUrl":"https:\/\/www.amyloidosisalliance.org\/wp-content\/uploads\/2026\/09\/logo.png","width":252,"height":252,"caption":"Amyloidosis Alliance"},"image":{"@id":"https:\/\/www.amyloidosisalliance.org\/nl\/#\/schema\/logo\/image\/"},"sameAs":["https:\/\/www.facebook.com\/AmyloidosisAlliance\/","https:\/\/x.com\/amyloidosisa"]}]}},"_links":{"self":[{"href":"https:\/\/www.amyloidosisalliance.org\/nl\/wp-json\/wp\/v2\/posts\/4736","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.amyloidosisalliance.org\/nl\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.amyloidosisalliance.org\/nl\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.amyloidosisalliance.org\/nl\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.amyloidosisalliance.org\/nl\/wp-json\/wp\/v2\/comments?post=4736"}],"version-history":[{"count":1,"href":"https:\/\/www.amyloidosisalliance.org\/nl\/wp-json\/wp\/v2\/posts\/4736\/revisions"}],"predecessor-version":[{"id":4737,"href":"https:\/\/www.amyloidosisalliance.org\/nl\/wp-json\/wp\/v2\/posts\/4736\/revisions\/4737"}],"wp:attachment":[{"href":"https:\/\/www.amyloidosisalliance.org\/nl\/wp-json\/wp\/v2\/media?parent=4736"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.amyloidosisalliance.org\/nl\/wp-json\/wp\/v2\/categories?post=4736"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.amyloidosisalliance.org\/nl\/wp-json\/wp\/v2\/tags?post=4736"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}