{"id":1608,"date":"2018-09-19T11:04:43","date_gmt":"2018-09-19T01:04:43","guid":{"rendered":"https:\/\/lungfoundation.com.au\/?page_id=1608"},"modified":"2023-04-05T15:08:32","modified_gmt":"2023-04-05T05:08:32","slug":"child","status":"publish","type":"page","link":"https:\/\/lungfoundation.com.au\/health-professionals\/conditions\/child\/","title":{"rendered":"Childhood Interstitial Lung Disease (chILD)"},"content":{"rendered":"","protected":false},"excerpt":{"rendered":"","protected":false},"author":1,"featured_media":6725,"parent":1497,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-1608","page","type-page","status-publish","has-post-thumbnail","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Childhood Interstitial Lung Disease (chILD) - Lung Foundation Australia<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/lungfoundation.com.au\/health-professionals\/conditions\/child\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Childhood Interstitial Lung Disease (chILD) - 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We know that families dealing with a rare disease, such as childhood interstitial lung disease (chILD) face very similar challenges including:<\/p>\n<ul class=\"ul1\">\n<li class=\"li2\"><span class=\"s1\">Delays in diagnosis and treatment due to limited awareness of their condition <\/span><\/li>\n<li class=\"li2\"><span class=\"s1\">Difficulty accessing information, the best service and treatment, either because of locality or because one does not exist<\/span><\/li>\n<li class=\"li2\"><span class=\"s1\">Difficulty navigating the health system and accessing support, whether this is in the form of equipment, financial or peer support<\/span><\/li>\n<li class=\"li1\"><span class=\"s1\">Difficulty finding a doctor to transition a child with a rare disease to appropriate adult services.<\/span><\/li>\n<\/ul>\n","button_display_setting":true,"button":{"":null,"button_type":"Link Button","link":{"title":"Find out more about chILD","url":"https:\/\/lungfoundation.com.au\/patients-carers\/living-with-a-lung-disease\/childhood-lung-disease\/overview\/","target":""},"email":"","file":false,"modal_trigger":"","button_text":""},"background_colour":"transparent","column_image":false,"youtube_video_url":""},{"column_type":"video","heading_text":"","paragraph_text":"","button_display_setting":false,"button":{"":null,"button_type":"Link Button","link":null,"email":"","file":false,"modal_trigger":"","button_text":""},"background_colour":"transparent","column_image":{"ID":2681,"id":2681,"title":"Prof Adam Jaffe","filename":"Prof-Adam-Jaffe.jpg","filesize":42498,"url":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe.jpg","link":"https:\/\/lungfoundation.com.au\/health-professionals\/conditions\/child\/prof-adam-jaffe\/","alt":"","author":"3","description":"","caption":"","name":"prof-adam-jaffe","status":"inherit","uploaded_to":1608,"date":"2018-09-24 07:44:36","modified":"2018-09-24 07:44:36","menu_order":0,"mime_type":"image\/jpeg","type":"image","subtype":"jpeg","icon":"https:\/\/lungfoundation.com.au\/wp-includes\/images\/media\/default.png","width":850,"height":583,"sizes":{"thumbnail":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe-150x150.jpg","thumbnail-width":150,"thumbnail-height":150,"medium":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe-300x206.jpg","medium-width":300,"medium-height":206,"medium_large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe-768x527.jpg","medium_large-width":768,"medium_large-height":527,"large":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe.jpg","large-width":850,"large-height":583,"1536x1536":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe.jpg","1536x1536-width":850,"1536x1536-height":583,"2048x2048":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe.jpg","2048x2048-width":850,"2048x2048-height":583,"xxlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe.jpg","xxlarge-width":850,"xxlarge-height":583,"xlarge":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe.jpg","xlarge-width":850,"xlarge-height":583,"header-navigation":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe-480x583.jpg","header-navigation-width":480,"header-navigation-height":583,"link-category":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe-380x256.jpg","link-category-width":380,"link-category-height":256,"card":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe-450x450.jpg","card-width":450,"card-height":450,"gform-image-choice-sm":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe.jpg","gform-image-choice-sm-width":300,"gform-image-choice-sm-height":206,"gform-image-choice-md":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe.jpg","gform-image-choice-md-width":400,"gform-image-choice-md-height":274,"gform-image-choice-lg":"https:\/\/lungfoundation.com.au\/wp-content\/uploads\/2018\/09\/Prof-Adam-Jaffe.jpg","gform-image-choice-lg-width":600,"gform-image-choice-lg-height":412}},"youtube_video_url":"https:\/\/www.youtube.com\/watch?v=Qa7uzWQ7N78"}]},{"acf_fc_layout":"wysiwyg_content_area","heading":"","content":"<p>Lung Foundation Australia is working to fill these gaps through a range of resources and initiatives outlined below.<\/p>\n<h3>Young Lungs Program<\/h3>\n<p>Our Young Lungs Program brings national experts together with parents of patients and other key stakeholders around the country to raise awareness and increase support for children with chILD and other rare lung diseases. To find out more, please <a href=\"https:\/\/lungfoundation.com.au\/contact\/\">contact us<\/a>.<\/p>\n","link":""},{"acf_fc_layout":"featured_posts_static","heading":"Resources","view_more_link":"","posts":[{"ID":1845,"post_author":"3","post_date":"2018-09-20 09:59:18","post_date_gmt":"2018-09-19 23:59:18","post_content":"<!-- wp:paragraph -->\n<p>This resource introduces Childhood Interstitial Lung Disease (chILD) and discusses the following topics:<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:list -->\n<ul><li>Disease subtypes<\/li><li>Symptoms<\/li><li>Causes<\/li><li>Diagnosis<\/li><li>Experience<\/li><li>Treatment<\/li><li>Management strategies<br>For further information on chILD you can visit our <a href=\"https:\/\/lungfoundation.com.au\/patients-carers\/living-with-a-lung-disease\/childhood-lung-disease\/overview\/\">website<\/a> or contact our Information and Support Centre on<a href=\"Tel:1800654301\"> 1800 654 301.<\/a><\/li><\/ul>\n<!-- \/wp:list -->\n\n<!-- wp:paragraph -->\n<p><\/p>\n<!-- \/wp:paragraph -->","post_title":"Childhood Interstitial Lung Disease","post_excerpt":"The Childhood Interstitial Lung Disease (chILD) fact sheet provides an overview of the disease, symptoms, causes, diagnosis, treatment, and management.","post_status":"publish","comment_status":"open","ping_status":"closed","post_password":"","post_name":"childrens-interstitial-lung-disease-child-fact-sheet","to_ping":"","pinged":"","post_modified":"2021-03-17 10:53:58","post_modified_gmt":"2021-03-17 00:53:58","post_content_filtered":"","post_parent":0,"guid":"https:\/\/lungfoundation.com.au\/?post_type=resource&#038;p=1845","menu_order":0,"post_type":"resource","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":11938,"post_author":"85","post_date":"2020-12-15 09:54:26","post_date_gmt":"2020-12-14 23:54:26","post_content":"<!-- wp:paragraph -->\n<p>This is a standard operating procedure (SOP) for biopsy practice in childhood interstitial lung disease (chILD). <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>This SOP has been developed by experts in paediatric rare lung disease using current chILD literature in line with ratified SOPs for broader paediatric practice. <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>It provides a checklist on diagnostic findings and references used. <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>For further information contact our&nbsp;<a href=\"https:\/\/lungfoundation.com.au\/patients-carers\/support-services\/support\/\">Information and Support Centre<\/a>&nbsp;on&nbsp;<a href=\"tel:1800654301\">1800 654 301.<\/a><\/p>\n<!-- \/wp:paragraph -->","post_title":"chILD Standardised Operating Procedure \u2013 Biopsy","post_excerpt":"This SOP documents best biopsy practice in chILD. This resource was developed in line with ratified SOP's for broader paediatric practice.","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"child-standardised-operating-procedure-biopsy","to_ping":"","pinged":"","post_modified":"2021-05-14 10:01:12","post_modified_gmt":"2021-05-14 00:01:12","post_content_filtered":"","post_parent":0,"guid":"http:\/\/lungfoundation.com.au\/?post_type=resource&#038;p=11938","menu_order":0,"post_type":"resource","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":11941,"post_author":"85","post_date":"2020-12-15 09:57:49","post_date_gmt":"2020-12-14 23:57:49","post_content":"<!-- wp:paragraph -->\n<p>This is a standard operating procedure (SOP) for bronchoscopy and bronchoalveolar lavage (BAL) practice in childhood interstitial lung disease (chILD). <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>This SOP has been developed by experts in paediatric rare lung disease using current chILD literature in line with ratified SOPs for broader paediatric practice. <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>It provides a checklist on diagnostic findings and references used. <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>For further information contact our I<a href=\"https:\/\/lungfoundation.com.au\/patients-carers\/support-services\/support\/\">nformation and Support Centre<\/a> on <a href=\"Tel:1800654301\">1800 654 301.<\/a><\/p>\n<!-- \/wp:paragraph -->","post_title":"chILD Standardised Operating Procedure \u2013 Bronchoscopy and BAL","post_excerpt":"This SOP documents best Bronchoscopy and BAL practice in chILD. The resource was developed in line with ratified SOPs for broader paediatric practice.\n","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"child-standardised-operating-procedure-bronchoscopy-and-bal","to_ping":"","pinged":"","post_modified":"2021-03-16 08:51:53","post_modified_gmt":"2021-03-15 22:51:53","post_content_filtered":"","post_parent":0,"guid":"http:\/\/lungfoundation.com.au\/?post_type=resource&#038;p=11941","menu_order":0,"post_type":"resource","post_mime_type":"","comment_count":"0","filter":"raw"}]},{"acf_fc_layout":"featured_posts_static","heading":"","view_more_link":null,"posts":[{"ID":11937,"post_author":"85","post_date":"2020-12-15 09:53:27","post_date_gmt":"2020-12-14 23:53:27","post_content":"<!-- wp:paragraph -->\n<p>This is a standard operating procedure (SOP) for genetic testing practice in childhood interstitial lung disease (chILD). <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>This SOP has been developed by experts in paediatric rare lung disease using current chILD literature in line with ratified SOPs for broader paediatric practice. <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>It provides a checklist on diagnostic findings and references used. <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>For further information contact our\u00a0<a href=\"https:\/\/lungfoundation.com.au\/patients-carers\/support-services\/support\/\">Information and Support Centre<\/a>\u00a0on\u00a0<a href=\"tel:1800654301\">1800 654 301.<\/a><\/p>\n<!-- \/wp:paragraph -->","post_title":"chILD Standardised Operating Procedure \u2013 Genetic Testing","post_excerpt":"This SOP documents best genetic testing practice in chILD. The resource was developed in line with ratified SOPs for broader paediatric practice.\n","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"child-standardised-operating-procedure-genetic-testing","to_ping":"","pinged":"","post_modified":"2021-03-16 09:26:14","post_modified_gmt":"2021-03-15 23:26:14","post_content_filtered":"","post_parent":0,"guid":"http:\/\/lungfoundation.com.au\/?post_type=resource&#038;p=11937","menu_order":0,"post_type":"resource","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":11930,"post_author":"85","post_date":"2020-12-15 09:52:18","post_date_gmt":"2020-12-14 23:52:18","post_content":"<!-- wp:paragraph -->\n<p>This is a standard operating procedure (SOP) for radiology practice in childhood interstitial lung disease (chILD). <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>This SOP has been developed by experts in paediatric rare lung disease using current chILD literature in line with ratified SOPs for broader paediatric practice. <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>It provides a checklist on diagnostic findings and references used. <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>For further information contact our\u00a0<a href=\"https:\/\/lungfoundation.com.au\/patients-carers\/support-services\/support\/\">Information and Support Centre<\/a>\u00a0on\u00a0<a href=\"tel:1800654301\">1800 654 301.<\/a><\/p>\n<!-- \/wp:paragraph -->","post_title":"chILD Standardised Operating Procedure \u2013 Radiology","post_excerpt":"This SOP documents best radiology practice in chILD. The resource was developed in line with ratified SOPs for broader paediatric practice.\n","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"child-standardised-operating-procedure-radiology","to_ping":"","pinged":"","post_modified":"2021-03-16 09:20:40","post_modified_gmt":"2021-03-15 23:20:40","post_content_filtered":"","post_parent":0,"guid":"http:\/\/lungfoundation.com.au\/?post_type=resource&#038;p=11930","menu_order":0,"post_type":"resource","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":11939,"post_author":"85","post_date":"2020-12-15 09:55:34","post_date_gmt":"2020-12-14 23:55:34","post_content":"<!-- wp:paragraph -->\n<p>This is a standard operating procedure (SOP) for spirometry practice in childhood interstitial lung disease (chILD). <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>This SOP has been developed by experts in paediatric rare lung disease using current chILD literature in line with ratified SOPs for broader paediatric practice. <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>This resource provides a checklist on diagnostic findings and references used. <\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>For further information contact our <a href=\"https:\/\/lungfoundation.com.au\/patients-carers\/support-services\/support\/\">Information and Support Centre<\/a> on <a href=\"tel:1800654301\">1800 654 301.<\/a><\/p>\n<!-- \/wp:paragraph -->","post_title":"chILD Standardised Operating Procedure \u2013 Spirometry","post_excerpt":"This SOP documents best spirometry practice in chILD. 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