{"id":15,"date":"2025-10-06T21:56:40","date_gmt":"2025-10-06T19:56:40","guid":{"rendered":"https:\/\/aliancamillionsmissing.org\/?page_id=15"},"modified":"2026-05-20T15:17:54","modified_gmt":"2026-05-20T14:17:54","slug":"inicio","status":"publish","type":"page","link":"https:\/\/aliancamillionsmissing.org\/en\/","title":{"rendered":"Home"},"content":{"rendered":"
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An association of patients, family members, and allies<\/h2><\/div>\n\n\n\n

We work to give a voice to people with Myalgic Encephalomyelitis (ME\/CFS), Long COVID, and other acute-onset post-infectious syndromes (PAIS).<\/p>\n\n\n\n

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How to participate<\/a><\/div>\n\n\n\n
Support<\/a><\/div>\n<\/div>\n<\/div>\n\n\n\n
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About us<\/h2><\/div>\n<\/div>\n\n\n\n
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Alian\u00e7a Millions Missing is a non-profit organization that advocates for the rights of people with Myalgic Encephalomyelitis (ME\/CFS), Long COVID, and other acute-onset post-infectious syndromes.<\/p>\n\n\n\n

Created in 2018 and formalized in 2025, AMM operates in Portugal, Brazil, and Portuguese-speaking communities, promoting scientific research, professional training, effective public policies, and awareness campaigns.<\/p>\n\n\n\n

What sets us apart<\/strong>: AMM is led by patients, ensuring that all decisions are based on the real experiences of those affected, in close collaboration with the scientific community.<\/p>\n\n\n\n

No one chooses to have these diseases. That is why AMM ensures that all services and support are provided free of charge and universally, whether or not patients are registered as members.<\/p>\n<\/div>\n<\/div>\n<\/div><\/div>\n\n\n\n

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Join us<\/h3><\/div>\n\n\n\n

AMM is open to all individuals and entities who want to contribute to its mission. You can register as a Member or as a Friend.<\/p>\n<\/div>\n\n\n\n

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Learn more<\/h3><\/div>\n\n\n\n

Information about diseases. AMM works on several fronts to transform scientific knowledge into real impact on patients' lives.<\/p>\n<\/div>\n\n\n\n

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Resources<\/h3><\/div>\n\n\n\n

AMM guides patients, families, professionals, and civil society to current and credible sources of clinical, scientific, and support information.<\/p>\n<\/div>\n<\/div><\/div>\n\n\n\n

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\"2\u00aa<\/figure><\/div>\n<\/div>\n\n\n\n
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2\u00aa CONFER\u00caNCIA INTERNACIONAL
Avan\u00e7os Cl\u00ednicos e Cient\u00edficos em
ENCEFALOMIELITE MI\u00c1LGICA e COVID Longa<\/strong><\/h2><\/div>\n<\/div>\n<\/div>\n\n\n\n
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NOVEMBER<\/h3><\/div>\n\n\n\n

12-13<\/h2>
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2025<\/h3><\/div>\n<\/div>\n\n\n\n
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AT<\/h3><\/div>\n\n\n\n

ORDEM
DOS M\u00c9DICOS<\/strong><\/h3><\/div>\n\n\n\n

NO PORTO<\/strong><\/h3><\/div>\n<\/div>\n\n\n\n
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More info<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n
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 \u201cEvery voice counts.
Together, we are stronger.\u201d<\/h2><\/div>\n<\/div>\n\n\n\n
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We invite everyone to
join us.<\/h2>\n\n\n\n

Join our community.
You can sign up as a Member (symbolic annual fee + voting rights at the General Meeting) or as a Friend (supporting member).<\/p>\n\n\n\n

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I Want to Register<\/a><\/div>\n<\/div>\n<\/div><\/div>\n<\/div>\n\n\n\n
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<\/p>\n\n\n\n

Pol\u00edtica de Privacidade<\/a><\/p>\n\n\n\n

<\/p>","protected":false},"excerpt":{"rendered":"

Uma associa\u00e7\u00e3o de doentes, familiares e aliados Trabalhamos para dar voz \u00e0s pessoas com Encefalomielite Mi\u00e1lgica (EM\/SFC), COVID Longa e outras s\u00edndromes p\u00f3s-infecciosas de instala\u00e7\u00e3o aguda (PAIS). Sobre n\u00f3s A Associa\u00e7\u00e3o Alian\u00e7a Millions Missing (AMM) \u00e9 uma organiza\u00e7\u00e3o sem fins lucrativos que defende os direitos das pessoas com Encefalomielite Mi\u00e1lgica (EM\/SFC), COVID Longa e outras… Home<\/span><\/a><\/p>","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_uag_custom_page_level_css":"","neve_meta_sidebar":"","neve_meta_container":"","neve_meta_enable_content_width":"on","neve_meta_content_width":100,"neve_meta_title_alignment":"","neve_meta_author_avatar":"","neve_post_elements_order":"","neve_meta_disable_header":"","neve_meta_disable_footer":"","neve_meta_disable_title":"on","_themeisle_gutenberg_block_has_review":false,"footnotes":""},"class_list":["post-15","page","type-page","status-publish","hentry"],"uagb_featured_image_src":{"full":false,"thumbnail":false,"medium":false,"medium_large":false,"large":false,"1536x1536":false,"2048x2048":false,"trp-custom-language-flag":false,"neve-blog":false},"uagb_author_info":{"display_name":"AMM","author_link":"https:\/\/aliancamillionsmissing.org\/en\/author\/amm\/"},"uagb_comment_info":0,"uagb_excerpt":"Uma associa\u00e7\u00e3o de doentes, familiares e aliados Trabalhamos para dar voz \u00e0s pessoas com Encefalomielite Mi\u00e1lgica (EM\/SFC), COVID Longa e outras s\u00edndromes p\u00f3s-infecciosas de instala\u00e7\u00e3o aguda (PAIS). Sobre n\u00f3s A Associa\u00e7\u00e3o Alian\u00e7a Millions Missing (AMM) \u00e9 uma organiza\u00e7\u00e3o sem fins lucrativos que defende os direitos das pessoas com Encefalomielite Mi\u00e1lgica (EM\/SFC), COVID Longa e outras… In\u00edcio","_links":{"self":[{"href":"https:\/\/aliancamillionsmissing.org\/en\/wp-json\/wp\/v2\/pages\/15","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/aliancamillionsmissing.org\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/aliancamillionsmissing.org\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/aliancamillionsmissing.org\/en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/aliancamillionsmissing.org\/en\/wp-json\/wp\/v2\/comments?post=15"}],"version-history":[{"count":290,"href":"https:\/\/aliancamillionsmissing.org\/en\/wp-json\/wp\/v2\/pages\/15\/revisions"}],"predecessor-version":[{"id":1500,"href":"https:\/\/aliancamillionsmissing.org\/en\/wp-json\/wp\/v2\/pages\/15\/revisions\/1500"}],"wp:attachment":[{"href":"https:\/\/aliancamillionsmissing.org\/en\/wp-json\/wp\/v2\/media?parent=15"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}