{"id":26140,"date":"2026-04-30T09:00:40","date_gmt":"2026-04-30T13:00:40","guid":{"rendered":"https:\/\/www.emilysentourage.org\/?p=26140"},"modified":"2026-04-30T16:48:01","modified_gmt":"2026-04-30T20:48:01","slug":"cf-unseen-a-new-perspective-for-cf-awareness-month","status":"publish","type":"post","link":"https:\/\/www.emilysentourage.org\/sv\/cf-unseen-a-new-perspective-for-cf-awareness-month\/","title":{"rendered":"CF, Osynlig: Ett nytt perspektiv f\u00f6r medvetenhetsm\u00e5naden f\u00f6r cystisk fibros"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">M\u00e5naden f\u00f6r medvetenhet om cystisk fibros (CFA) b\u00f6rjar idag \u2013 och p\u00e5 Emily\u2019s Entourage (EE) bjuder vi in dig att titta n\u00e4rmare.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Eftersom n\u00e4r det g\u00e4ller cystisk fibros (CF), <\/span><b>Det du ser \u00e4r bara en del av historien.<\/b><\/p>\n<p><img fetchpriority=\"high\" decoding=\"async\" class=\"aligncenter wp-image-26145\" src=\"https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Header-Graphic-3.png\" alt=\"\" width=\"834\" height=\"417\" srcset=\"https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Header-Graphic-3.png 1024w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Header-Graphic-3-300x150.png 300w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Header-Graphic-3-768x384.png 768w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Header-Graphic-3-18x9.png 18w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Header-Graphic-3-600x300.png 600w\" sizes=\"(max-width: 834px) 100vw, 834px\" \/><\/p>\n<p><span style=\"font-weight: 400;\">CF \u00e4r en osynlig sjukdom. De verkligheter som pr\u00e4glar livet med CF \u2013 dagliga behandlingar, den fysiska p\u00e5frestningen, den mentala b\u00f6rdan, os\u00e4kerheten, r\u00e4dslan \u2013 \u00e4r ofta dolda f\u00f6r \u00f6gat. <\/span><b>Men bara f\u00f6r att dessa upplevelser inte alltid \u00e4r synliga g\u00f6r det dem inte mindre verkliga.<\/b><\/p>\n<p><span style=\"font-weight: 400;\">\u00c4ven om utvecklingen av livr\u00e4ddande, mutationsriktade behandlingar har f\u00f6r\u00e4ndrat livet f\u00f6r n\u00e4stan 90% personer med cystisk fibros, v\u00e4ntar fortfarande de \u00e5terst\u00e5ende 10% som inte har nytta av dessa behandlingar. De lever fortfarande p\u00e5 l\u00e5nad tid. De k\u00e4mpar fortfarande med samma f\u00f6r\u00f6dande sjukdom som cystisk fibros alltid har varit. De k\u00e4mpar fortfarande med alla krafter f\u00f6r att h\u00e5lla fast vid hoppet.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Varje \u00e5r, under cystisk fibros-informationsm\u00e5nad i maj, samlas vi kring v\u00e5rt st\u00f6rsta och dj\u00e4rvaste m\u00e5l: att <\/span><b>#CrossOutCF \u2013 f\u00f6r 100% i CF-gemenskapen, en g\u00e5ng f\u00f6r alla.<\/b><\/p>\n<p><span style=\"font-weight: 400;\">Den h\u00e4r m\u00e5naden \u00e5teruppfinner vi vad det inneb\u00e4r.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Vi stryker antaganden.<\/span><span style=\"font-weight: 400;\"><br \/>\n<\/span><span style=\"font-weight: 400;\">Vi stryker ytliga uppfattningar.<\/span><span style=\"font-weight: 400;\"><br \/>\n<\/span><span style=\"font-weight: 400;\">Vi stryker \u00f6ver det v\u00e4rlden tror sig veta om CF \u2013<\/span><span style=\"font-weight: 400;\"><br \/>\n<\/span><span style=\"font-weight: 400;\">och avsl\u00f6ja vad som d\u00f6ljer sig bakom kulisserna.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Du kanske f\u00e5r se ett leende.<\/span><span style=\"font-weight: 400;\"><br \/>\n<\/span><span style=\"font-weight: 400;\">Men du ser inte de fyra timmarna av dagliga behandlingar bakom det.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Det kan h\u00e4nda att du ser n\u00e5gon som verkar leva sitt allra b\u00e4sta liv.<\/span><span style=\"font-weight: 400;\"><br \/>\n<\/span><span style=\"font-weight: 400;\">Men du ser inte det h\u00e5rda arbete och den uth\u00e5llighet som kr\u00e4vs bara f\u00f6r att dyka upp.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Du kanske st\u00f6ter p\u00e5 en rubrik som v\u00e4cker uppm\u00e4rksamhet.<\/span><span style=\"font-weight: 400;\"><br \/>\n<\/span><span style=\"font-weight: 400;\">Men man ser inte alla de \u00e5r av forskning som har gjort det m\u00f6jligt.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Vi lyfter p\u00e5 sl\u00f6jan \u2013 vi delar med oss av de r\u00e5a, m\u00e4nskliga verkligheterna i livet med cystisk fibros och ger r\u00f6st \u00e5t dem som alltf\u00f6r ofta inte blir h\u00f6rda.\u00a0<\/span><\/p>\n<h3><b>En m\u00e5nad med verkliga ber\u00e4ttelser, verkliga r\u00f6ster och verkliga liv med cystisk fibros<\/b><\/h3>\n<p><span style=\"font-weight: 400;\">Under hela maj m\u00e5nad s\u00e4tter vi ljuset p\u00e5 de upplevelser som formar vardagslivet med cystisk fibros f\u00f6r att visa det som ofta f\u00f6rblir osynligt:<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Ber\u00e4ttelser fr\u00e5n m\u00e4nniskor som lever med cystisk fibros i resurssvaga delar av v\u00e4rlden.<\/span><span style=\"font-weight: 400;\"><br \/>\n<\/span><span style=\"font-weight: 400;\">Ber\u00e4ttelser fr\u00e5n personer som lever med komplexa komorbiditeter som f\u00f6rsv\u00e5rar en redan utmanande sjukdom.<\/span><span style=\"font-weight: 400;\"><br \/>\n<\/span><span style=\"font-weight: 400;\">Ber\u00e4ttelser fr\u00e5n m\u00e4nniskor som har genomg\u00e5tt en transplantation \u2013 tv\u00e5 g\u00e5nger.<\/span><span style=\"font-weight: 400;\"><br \/>\n<\/span><span style=\"font-weight: 400;\">Ber\u00e4ttelser fr\u00e5n de sista 10%, som forts\u00e4tter att h\u00e5lla fast vid hoppet medan vetenskapen arbetar f\u00f6r att hinna ikapp.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Dessa r\u00f6ster speglar djupet, motst\u00e5ndskraften och m\u00e5ngfalden i CF-gemenskapen \u2013 och p\u00e5minner oss om att \u00e4ven om CF kan vara osynligt, \u00e4r dess inverkan allt annat \u00e4n det.<\/span><\/p>\n<h3><b>Hur du kan engagera dig<\/b><\/h3>\n<p><span style=\"font-weight: 400;\">Denna m\u00e5nad handlar om medvetenhet, gemenskap och samh\u00f6righet. Varje ber\u00e4ttelse som delas, varje perspektiv som lyfts fram och varje konversation som v\u00e4cks hj\u00e4lper till att synligg\u00f6ra verkligheten med cystisk fibros \u2013 och f\u00f6r oss n\u00e4rmare varandra <\/span><b>mot en framtid d\u00e4r det finns livr\u00e4ddande behandlingar f\u00f6r 100% inom cystisk fibros-gruppen och ingen l\u00e4mnas utanf\u00f6r.<\/b><\/p>\n<p><img decoding=\"async\" class=\"aligncenter wp-image-26147\" src=\"https:\/\/www.emilysentourage.org\/wp-content\/uploads\/Kickoff-Post-B-2-819x1024.png\" alt=\"\" width=\"490\" height=\"614\" srcset=\"https:\/\/www.emilysentourage.org\/wp-content\/uploads\/Kickoff-Post-B-2-819x1024.png 819w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/Kickoff-Post-B-2-240x300.png 240w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/Kickoff-Post-B-2-768x960.png 768w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/Kickoff-Post-B-2-10x12.png 10w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/Kickoff-Post-B-2-440x550.png 440w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/Kickoff-Post-B-2-600x750.png 600w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/Kickoff-Post-B-2.png 1080w\" sizes=\"(max-width: 490px) 100vw, 490px\" \/><\/p>\n<ul>\n<li style=\"font-weight: 400;\" aria-level=\"1\"><b>H\u00e5ll dig uppkopplad<\/b><b><br \/>\n<\/b><span style=\"font-weight: 400;\">F\u00f6lj med p\u00e5 <a href=\"https:\/\/www.facebook.com\/EmilysEntourage\" target=\"_blank\" rel=\"noopener\">Facebook,<\/a> <a href=\"https:\/\/www.instagram.com\/emilysentourage\/\" target=\"_blank\" rel=\"noopener\">Instagram<\/a>, <a href=\"https:\/\/www.linkedin.com\/company\/emilysentourage\/\" target=\"_blank\" rel=\"noopener\">LinkedIn<\/a>, och <a href=\"https:\/\/x.com\/EmilysEntourage\/\" target=\"_blank\" rel=\"noopener\">X<\/a> Under hela maj m\u00e5nad kommer vi att lyfta fram olika perspektiv fr\u00e5n hela CF-gemenskapen \u2013 allt fr\u00e5n egna erfarenheter och personliga ber\u00e4ttelser till banbrytande forskning och v\u00e4garna mot nya behandlingar. Gl\u00f6m inte att <a href=\"https:\/\/www.emilysentourage.org\/sv\/eeupdates\/\" target=\"_blank\" rel=\"noopener\">anm\u00e4l dig till v\u00e5r <em>EE Insider<\/em> nyhetsbrev<\/a>!<\/span><\/li>\n<li style=\"font-weight: 400;\" aria-level=\"1\"><b>Delta i konversationen<\/b><b><br \/>\n<\/b><span style=\"font-weight: 400;\">Din r\u00f6st \u00e4r viktig. Dela din CF-ber\u00e4ttelse \u2013 eller hj\u00e4lp till att f\u00f6rst\u00e4rka andras \u2013 med hj\u00e4lp av <\/span><b>#CrossOutCF<\/b><span style=\"font-weight: 400;\"> och <\/span><b>#SpeakUpCF<\/b><span style=\"font-weight: 400;\">. Hj\u00e4lp oss att belysa hur livet med cystisk fibros verkligen ser ut \u2013 och varf\u00f6r livr\u00e4ddande genombrott inte kan v\u00e4nta. Dina gillamarkeringar, dina kommentarer och dina delningar betyder mycket!!\u00a0<\/span><\/li>\n<li style=\"font-weight: 400;\" aria-level=\"1\"><b>Vidta \u00e5tg\u00e4rder<\/b><b><br \/>\n<\/b><b>Donera, engagera dig, sprid budskapet. Varje insats <\/b><span style=\"font-weight: 400;\">lyfter fram de upplevelser som alltf\u00f6r ofta f\u00f6rblir osynliga och f\u00f6r oss n\u00e4rmare det slutgiltiga m\u00e5let.\u00a0<\/span><\/li>\n<\/ul>\n<p><span style=\"font-weight: 400;\">Eftersom vi n\u00e4r vi avsl\u00f6jar hela bilden av CF st\u00e4rker v\u00e5r gemenskap och r\u00f6r oss n\u00e4rmare en framtid d\u00e4r vi <\/span><b>#CrossOutCF till alla s\u00e5 snart som m\u00f6jligt. Den framtiden kan inte b\u00f6rja f\u00f6rr!<\/b><\/p>\n<h3 style=\"text-align: center;\"><b>Tack till v\u00e5ra sponsorer f\u00f6r CF Awareness Month<\/b><\/h3>\n<p><span style=\"font-weight: 400;\">Vi vill tacka v\u00e5ra gener\u00f6sa sponsorer f\u00f6r kampanjen \u201dCystic Fibrosis Awareness Month 2026\u201d. Ert st\u00f6d hj\u00e4lper oss att ge r\u00f6sten \u00e5t CF-gemenskapen och p\u00e5skynda livr\u00e4ddande genombrott f\u00f6r den sista 10%.<\/span><\/p>\n<p><img decoding=\"async\" class=\"wp-image-26143 size-large aligncenter\" src=\"https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Sponsors-Updated--1024x950.png\" alt=\"\" width=\"960\" height=\"891\" srcset=\"https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Sponsors-Updated--1024x950.png 1024w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Sponsors-Updated--300x278.png 300w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Sponsors-Updated--768x712.png 768w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Sponsors-Updated--1536x1425.png 1536w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Sponsors-Updated--2048x1900.png 2048w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Sponsors-Updated--13x12.png 13w, https:\/\/www.emilysentourage.org\/wp-content\/uploads\/2026-CFA-Sponsors-Updated--600x557.png 600w\" sizes=\"(max-width: 960px) 100vw, 960px\" \/><br style=\"font-weight: 400;\" \/><br style=\"font-weight: 400;\" \/><\/p>","protected":false},"excerpt":{"rendered":"<p>Cystic Fibrosis Awareness (CFA) Month begins today\u2014and at Emily\u2019s Entourage (EE), we\u2019re inviting you to look closer. Because when it comes to cystic fibrosis (CF), what you see is only part of the story. CF is an invisible disease. The realities that shape life with CF\u2014daily treatments, the physical toll, the mental load, the uncertainty,&#8230; <\/p>\n<div class=\"clear\"><\/div>\n<p><a href=\"https:\/\/www.emilysentourage.org\/sv\/cf-unseen-a-new-perspective-for-cf-awareness-month\/\" class=\"excerpt-read-more\">L\u00e4s mer om<\/a><\/p>","protected":false},"author":1719,"featured_media":26153,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_seopress_titles_title":"%%post_title%%","_seopress_titles_desc":"%%post_excerpt%%","_seopress_robots_index":"","_seopress_robots_follow":"","_seopress_robots_imageindex":"","_seopress_robots_snippet":"","_seopress_robots_primary_cat":"none","_seopress_robots_breadcrumbs":"","_seopress_robots_freeze_modified_date":"","_seopress_robots_custom_modified_date":"","_seopress_robots_canonical":"","_seopress_social_fb_title":"","_seopress_social_fb_desc":"","_seopress_social_fb_img":"","_seopress_social_fb_img_attachment_id":0,"_seopress_social_fb_img_width":0,"_seopress_social_fb_img_height":0,"_seopress_social_twitter_title":"","_seopress_social_twitter_desc":"","_seopress_social_twitter_img":"","_seopress_social_twitter_img_attachment_id":0,"_seopress_social_twitter_img_width":0,"_seopress_social_twitter_img_height":0,"_seopress_redirections_value":"","_seopress_redirections_enabled":"","_seopress_redirections_enabled_regex":"","_seopress_redirections_logged_status":"both","_seopress_redirections_param":"","_seopress_redirections_type":301,"_seopress_analysis_target_kw":"","_monsterinsights_skip_tracking":false,"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_feature_clip_id":0,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_post_was_ever_published":false},"categories":[1],"tags":[214,213,137],"class_list":["post-26140","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized","tag-cfa-month","tag-cystic-fibrosis-awareness","tag-cystic-fibrosis-awareness-month"],"acf":[],"jetpack_sharing_enabled":true,"jetpack_featured_media_url":"https:\/\/www.emilysentourage.org\/wp-content\/uploads\/WordPress-Featured-Image-11.png","post_mailing_queue_ids":[],"_links":{"self":[{"href":"https:\/\/www.emilysentourage.org\/sv\/wp-json\/wp\/v2\/posts\/26140","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.emilysentourage.org\/sv\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.emilysentourage.org\/sv\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.emilysentourage.org\/sv\/wp-json\/wp\/v2\/users\/1719"}],"replies":[{"embeddable":true,"href":"https:\/\/www.emilysentourage.org\/sv\/wp-json\/wp\/v2\/comments?post=26140"}],"version-history":[{"count":5,"href":"https:\/\/www.emilysentourage.org\/sv\/wp-json\/wp\/v2\/posts\/26140\/revisions"}],"predecessor-version":[{"id":26152,"href":"https:\/\/www.emilysentourage.org\/sv\/wp-json\/wp\/v2\/posts\/26140\/revisions\/26152"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.emilysentourage.org\/sv\/wp-json\/wp\/v2\/media\/26153"}],"wp:attachment":[{"href":"https:\/\/www.emilysentourage.org\/sv\/wp-json\/wp\/v2\/media?parent=26140"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.emilysentourage.org\/sv\/wp-json\/wp\/v2\/categories?post=26140"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.emilysentourage.org\/sv\/wp-json\/wp\/v2\/tags?post=26140"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}