{"id":234,"date":"2023-09-05T13:44:22","date_gmt":"2023-09-05T11:44:22","guid":{"rendered":"https:\/\/cfnorge.bwod.dev\/?page_id=234"},"modified":"2025-12-12T15:51:25","modified_gmt":"2025-12-12T14:51:25","slug":"cf-norge","status":"publish","type":"page","link":"https:\/\/cfnorge.no\/en\/","title":{"rendered":"CF Norge"},"content":{"rendered":"

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CF and PCD<\/h1>\n

[\/et_pb_text][et_pb_text _builder_version=»4.21.0″ _module_preset=»default» text_font=»Poppins|300|||||||» text_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ text_font_size=»16px» text_line_height=»1.8em» header_3_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ custom_margin=»||20px|||» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22text_text_color%22,%22header_3_text_color%22%93}»]<\/p>\n

Cystic Fibrosis (CF) is a congenital, severe genetic disorder that causes thick mucus to build up in the lungs, making them prone to infections.<\/p>\n

Primary Ciliary Dyskinesia (PCD) is a rare congenital condition caused by defects in the structure and function of the cilia, leading to mucus accumulation in the upper and lower airways.<\/span><\/p>\n

The Norwegian Association for Cystic Fibrosis (NFCF) is an organization for individuals diagnosed with cystic fibrosis and primary ciliary dyskinesia, as well as their families and caregivers.\u00a0<\/span><\/p>\n

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CF and PCD<\/h1>\n

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Cystic Fibrosis (CF) is a congenital, severe genetic disorder that causes thick mucus to build up in the lungs, making them prone to infections.\u00a0<\/span><\/p>\n

[\/et_pb_text][et_pb_image src=»https:\/\/cfnorge.no\/wp-content\/uploads\/2024\/09\/lunger-nettside-CF-Mobil.png» title_text=»lunger-nettside-CF-Mobil» _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][\/et_pb_image][et_pb_text _builder_version=»4.21.0″ _module_preset=»default» text_font=»Poppins|300|||||||» text_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ text_font_size=»16px» text_line_height=»1.8em» header_3_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ max_width=»80%» module_alignment=»center» custom_margin=»||38px|||» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22text_text_color%22,%22header_3_text_color%22%93}»]<\/p>\n

Primary Ciliary Dyskinesia (PCD) is a rare congenital condition caused by defects in the structure and function of the cilia, leading to mucus accumulation in the upper and lower airways.<\/span><\/p>\n

The Norwegian Association for Cystic Fibrosis (NFCF) is an organization for individuals diagnosed with cystic fibrosis and primary ciliary dyskinesia, as well as their families and caregivers.\u00a0<\/span><\/p>\n

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NEWS AND ARTICLES<\/h2>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=»4.21.0″ _module_preset=»default» custom_margin=»|auto|0px|auto|false|false» custom_padding=»||0px||false|false» locked=»off» global_colors_info=»{}»][et_pb_column type=»4_4″ _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][et_pb_blog fullwidth=»off» posts_number=»2″ include_categories=»all» use_manual_excerpt=»off» excerpt_length=»180″ show_more=»on» show_author=»off» show_date=»off» show_categories=»off» show_pagination=»off» masonry_tile_background_color=»RGBA(255,255,255,0)» disabled_on=»on|off|on» _builder_version=»4.21.0″ _module_preset=»default» header_font=»Poppins||||||||» header_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ header_line_height=»1.2em» body_font=»Poppins|300|||||||» body_text_align=»left» body_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ meta_font=»|700||on|||||» meta_text_color=»gcid-f60bfea8-f451-489d-8bfd-27e12ee36365″ meta_font_size=»12px» read_more_font=»Poppins|||on|||||» read_more_text_color=»gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05″ read_more_font_size=»16px» read_more_line_height=»2.6em» body_link_font=»Poppins|600|||||||» background_color=»RGBA(255,255,255,0)» text_orientation=»left» border_width_all=»0px» border_radii_image=»off|15px|15px||» global_colors_info=»{%22gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05%22:%91%22read_more_text_color%22%93,%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22body_text_color%22,%22header_text_color%22%93,%22gcid-f60bfea8-f451-489d-8bfd-27e12ee36365%22:%91%22meta_text_color%22%93}»][\/et_pb_blog][et_pb_blog fullwidth=»off» posts_number=»3″ include_categories=»all» use_manual_excerpt=»off» excerpt_length=»180″ show_more=»on» show_author=»off» show_date=»off» show_categories=»off» show_pagination=»off» masonry_tile_background_color=»RGBA(255,255,255,0)» disabled_on=»off|on|off» _builder_version=»4.21.0″ _module_preset=»default» header_font=»Poppins||||||||» header_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ header_line_height=»1.2em» body_font=»Poppins|300|||||||» body_text_align=»left» body_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ meta_font=»|700||on|||||» meta_text_color=»gcid-f60bfea8-f451-489d-8bfd-27e12ee36365″ meta_font_size=»12px» read_more_font=»Poppins|||on|||||» read_more_text_color=»gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05″ read_more_font_size=»16px» read_more_line_height=»2.6em» body_link_font=»Poppins|600|||||||» background_color=»RGBA(255,255,255,0)» text_orientation=»left» border_width_all=»0px» border_radii_image=»off|15px|15px||» global_colors_info=»{%22gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05%22:%91%22read_more_text_color%22%93,%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22body_text_color%22,%22header_text_color%22%93,%22gcid-f60bfea8-f451-489d-8bfd-27e12ee36365%22:%91%22meta_text_color%22%93}»][\/et_pb_blog][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=»4.21.0″ _module_preset=»default» custom_margin=»0px||||false|false» custom_padding=»0px||||false|false» global_colors_info=»{}»][et_pb_column type=»4_4″ _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][et_pb_text _builder_version=»4.21.0″ _dynamic_attributes=»link_option_url» _module_preset=»default» link_font=»Poppins|700|||on||||» link_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ link_font_size=»16px» header_2_font=»Poppins|600|||||||» header_2_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ custom_margin=»1px|||||» link_option_url=»@ET-DC@eyJkeW5hbWljIjp0cnVlLCJjb250ZW50IjoicG9zdF9saW5rX3VybF9wYWdlIiwic2V0dGluZ3MiOnsicG9zdF9pZCI6IjI1NSJ9fQ==@» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22header_2_text_color%22,%22link_text_color%22%93}»]<\/p>\n

See all news and articles here ><\/a><\/p>\n

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Number of people with CF in Norway<\/h3>\n

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18 years or older<\/span><\/h3>\n

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Children<\/h3>\n

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\"Being a grandmother is a gift. My grandchild is cheerful and full of life, despite cystic fibrosis which affects the lungs and stomach. We delight in his smile, but worry about treatments and infections. We adapt our lives to protect him, washing hands and being careful. Everything for our grandchild.\"<\/span><\/p>\n

- Grandmother to a child with CF<\/p>\n

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Number of people with PCD in Noray<\/h3>\n

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18 years or older<\/span><\/h3>\n

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Children<\/h3>\n

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Being a parent to a child with PCD means a lot of extra planning and care, but it also teaches you to appreciate the moments that are completely ordinary for others.<\/span><\/p>\n

\u2013 Father of a child with PCD<\/p>\n

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Need someone to talk to?<\/strong><\/h2>\n

NFCF has a nationwide network of contact persons, which we callpeers<\/a>. They are available for anyone who needs someone to talk to. They are either parents of children with CF or adults living with CF themselves. You can contact one of our peer supporters directly. We also have closed Facebook groups where you can chat with like-minded people.<\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=»1_4,1_4,1_4,1_4″ use_custom_gutter=»on» custom_padding_last_edited=»on|tablet» _builder_version=»4.21.0″ _module_preset=»default» custom_margin=»51px|auto||auto||» custom_padding=»68px|||||» custom_padding_tablet=»20px||||false|false» custom_padding_phone=»20px||||false|false» border_width_top=»1px» border_color_top=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22border_color_top%22%93}»][et_pb_column type=»1_4″ _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][et_pb_image src=»https:\/\/cfnorge.no\/wp-content\/uploads\/2024\/06\/Logo-NSCF-3.png» title_text=»Logo-NSCF-3″ url=»https:\/\/www.oslo-universitetssykehus.no\/fag-og-forskning\/nasjonale-og-regionale-tjenester\/norsk-senter-for-cystisk-fibrose» url_new_window=»on» _builder_version=»4.21.0″ _module_preset=»default» max_width_tablet=»80%» max_width_phone=»60%» max_width_last_edited=»on|phone» module_alignment=»center» custom_margin_tablet=»» custom_margin_phone=»-80px||||false|false» custom_margin_last_edited=»on|phone» custom_padding_tablet=»» custom_padding_phone=»0px||||false|false» custom_padding_last_edited=»on|phone» global_colors_info=»{}»][\/et_pb_image][\/et_pb_column][et_pb_column type=»1_4″ _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][et_pb_image src=»https:\/\/cfnorge.no\/wp-content\/uploads\/2024\/06\/Organdonasjon-logo-3.png» title_text=»Organdonasjon-logo-3″ url=»https:\/\/organdonasjon.no\/» url_new_window=»on» _builder_version=»4.21.0″ _module_preset=»default» max_width_tablet=»80%» max_width_phone=»60%» max_width_last_edited=»on|phone» module_alignment=»center» custom_margin_tablet=»-80px||||false|false» custom_margin_phone=»-80px||||false|false» custom_margin_last_edited=»on|phone» global_colors_info=»{}»][\/et_pb_image][\/et_pb_column][et_pb_column type=»1_4″ _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][et_pb_image src=»https:\/\/cfnorge.no\/wp-content\/uploads\/2024\/06\/Stiftelsen-DAM-logo.png» title_text=»Stiftelsen-DAM-logo» url=»https:\/\/dam.no\/» url_new_window=»on» _builder_version=»4.21.0″ _module_preset=»default» max_width_tablet=»80%» max_width_phone=»60%» max_width_last_edited=»on|phone» module_alignment=»center» custom_margin_tablet=»-80px||||false|false» custom_margin_phone=»-80px||||false|false» custom_margin_last_edited=»on|phone» global_colors_info=»{}»][\/et_pb_image][\/et_pb_column][et_pb_column type=»1_4″ _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][et_pb_image src=»https:\/\/cfnorge.no\/wp-content\/uploads\/2024\/06\/Viatris-logo.png» title_text=»Viatris-logo» url=»https:\/\/www.creon.no\/nb-no\/instruksjonsvideo?utm_medium=&utm_campaign=&utm_source=&utm_content=&utm_term=» url_new_window=»on» _builder_version=»4.21.0″ _module_preset=»default» max_width_tablet=»80%» max_width_phone=»60%» max_width_last_edited=»on|phone» module_alignment=»center» custom_margin_tablet=»-80px||||false|false» custom_margin_phone=»-80px||||false|false» custom_margin_last_edited=»on|phone» custom_padding=»||65px|||» custom_padding_tablet=»||65px|||» custom_padding_phone=»||0px||false|false» custom_padding_last_edited=»on|phone» global_colors_info=»{}»][\/et_pb_image][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=»1″ disabled_on=»on|on|off» _builder_version=»4.21.0″ _module_preset=»default» background_color=»gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05″ custom_padding=»21px||0px||false|false» locked=»off» global_colors_info=»{%22gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05%22:%91%22background_color%22%93}»][et_pb_row column_structure=»1_2,1_2″ _builder_version=»4.21.0″ _module_preset=»default» custom_margin=»13px|auto|0px|auto|false|false» custom_padding=»||0px||false|false» global_colors_info=»{}»][et_pb_column type=»1_2″ _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][et_pb_image src=»https:\/\/cfnorge.no\/wp-content\/uploads\/2023\/08\/Stott-oss-illustrasjon-CF-2-1.png» title_text=»St\u00f8tt-oss-illustrasjon-CF-2″ _builder_version=»4.21.0″ _module_preset=»default» width=»70%» module_alignment=»right» global_colors_info=»{}»][\/et_pb_image][\/et_pb_column][et_pb_column type=»1_2″ _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][et_pb_text _builder_version=»4.21.0″ _module_preset=»default» header_2_font=»Poppins|600|||||||» header_2_text_color=»#FFFFFF» header_2_font_size=»30px» header_3_font=»Poppins||||||||» header_3_text_color=»#FFFFFF» header_3_font_size=»20px» header_3_line_height=»1.5em» custom_margin=»86px|||||» global_colors_info=»{}»]<\/p>\n

Support us<\/h2>\n

We are grateful for all
contributions to our work.<\/h3>\n

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Support us<\/h2>\n

We are grateful for all
contributions to our work.<\/h3>\n

[\/et_pb_text][et_pb_button button_url=»@ET-DC@eyJkeW5hbWljIjp0cnVlLCJjb250ZW50IjoicG9zdF9saW5rX3VybF9wYWdlIiwic2V0dGluZ3MiOnsicG9zdF9pZCI6IjQ1NyJ9fQ==@» button_text=»LES HVORDAN HER» _builder_version=»4.21.0″ _dynamic_attributes=»button_url» _module_preset=»default» custom_button=»on» button_text_size=»16px» button_text_color=»#FFFFFF» button_bg_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ button_border_width=»0px» button_border_radius=»100px» custom_margin=»||11px|||» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22button_bg_color%22%93}»][\/et_pb_button][et_pb_image src=»https:\/\/cfnorge.no\/wp-content\/uploads\/2023\/08\/Stott-oss-illustrasjon-CF-2-1.png» title_text=»St\u00f8tt-oss-illustrasjon-CF-2″ _builder_version=»4.21.0″ _module_preset=»default» max_width=»64%» max_width_tablet=»50%» max_width_phone=»50%» max_width_last_edited=»on|tablet» module_alignment=»right» custom_margin_tablet=»-40px||||false|false» custom_margin_phone=»-40px||||false|false» custom_margin_last_edited=»on|tablet» global_colors_info=»{}»][\/et_pb_image][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>","protected":false},"excerpt":{"rendered":"

CF og PCDCystisk fibrose (CF) er en medf\u00f8dt, alvorlig genetisk multiorgansykdom som f\u00f8rer til seigt slim i lungene, som skaper grobunn for infeksjoner. Prim\u00e6r cili\u00e6r dyskinesi (PCD) er en sjelden og medf\u00f8dt sykdom som skyldes en feil i de bevegelige flimmerh\u00e5renes oppbygning og funksjon og f\u00f8rer til opphopning av slim i \u00f8vre og nedre luftveier. […]<\/p>","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"class_list":["post-234","page","type-page","status-publish","hentry"],"yoast_head":"\nCF Norge |\u00a0Norsk forening for cystisk fibrose<\/title>\n<meta name=\"description\" content=\"Norsk forening for cystisk fibrose er en medlemsorganisasjon for personer med diagnosene cystisk fibrose og prim\u00e6r cili\u00e6r dyskinesi.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/cfnorge.no\/en\/\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"CF Norge |\u00a0Norsk forening for cystisk fibrose\" \/>\n<meta property=\"og:description\" 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