Les NFCF sine brosjyrer HER<\/a><\/strong><\/p>\n <\/p>\n
[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=»4.21.0″ _module_preset=»default» 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″ _module_preset=»default» header_font=»Poppins|600|||||||» header_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ custom_margin=»0px||-9px||false|false» custom_padding=»0px||0px||false|false» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22header_text_color%22%93}»]<\/p>\n
Life stages\u00a0<\/h1>\n
[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=»1_3,1_3,1_3″ _builder_version=»4.21.0″ _module_preset=»default» custom_padding=»6px|||||» global_colors_info=»{}»][et_pb_column type=»1_3″ _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][et_pb_image src=»https:\/\/cfnorge.bwod.dev\/wp-content\/uploads\/2023\/09\/hollie-santos-aUtvHsu8Uzk-unsplash-scaled.jpg» title_text=»hollie-santos-aUtvHsu8Uzk-unsplash» _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][\/et_pb_image][et_pb_button button_url=»@ET-DC@eyJkeW5hbWljIjp0cnVlLCJjb250ZW50IjoicG9zdF9saW5rX3VybF9wYWdlIiwic2V0dGluZ3MiOnsicG9zdF9pZCI6Ijk4MyJ9fQ==@» button_text=»Barn med CF» button_alignment=»center» _builder_version=»4.21.0″ _dynamic_attributes=»button_url» _module_preset=»default» custom_button=»on» button_text_size=»18px» button_text_color=»#FFFFFF» button_bg_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ button_border_width=»0px» button_border_color=»RGBA(255,255,255,0)» button_border_radius=»91px» button_icon=»||fa||900″ button_icon_color=»#FFFFFF» button_on_hover=»off» custom_margin=»||10px||false|false» custom_padding=»10px|40px|10px|20px|false|false» button_text_shadow_style=»preset1″ locked=»off» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22button_bg_color%22%93}»][\/et_pb_button][\/et_pb_column][et_pb_column type=»1_3″ _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][et_pb_image src=»https:\/\/cfnorge.bwod.dev\/wp-content\/uploads\/2023\/09\/helena-lopes-PGnqT0rXWLs-unsplash-scaled.jpg» title_text=»helena-lopes-PGnqT0rXWLs-unsplash» _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][\/et_pb_image][et_pb_button button_url=»@ET-DC@eyJkeW5hbWljIjp0cnVlLCJjb250ZW50IjoicG9zdF9saW5rX3VybF9wYWdlIiwic2V0dGluZ3MiOnsicG9zdF9pZCI6IjEwMTAifX0=@» button_text=»Ung med CF» button_alignment=»center» _builder_version=»4.21.0″ _dynamic_attributes=»button_url» _module_preset=»default» custom_button=»on» button_text_size=»18px» button_text_color=»#FFFFFF» button_bg_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ button_border_width=»0px» button_border_color=»RGBA(255,255,255,0)» button_border_radius=»91px» button_icon=»||fa||900″ button_icon_color=»#FFFFFF» button_on_hover=»off» custom_margin=»||10px||false|false» custom_padding=»10px|40px|10px|20px|false|false» button_text_shadow_style=»preset1″ locked=»off» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22button_bg_color%22%93}»][\/et_pb_button][\/et_pb_column][et_pb_column type=»1_3″ _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][et_pb_image src=»https:\/\/cfnorge.bwod.dev\/wp-content\/uploads\/2024\/06\/iStock-1284869697.jpg» title_text=»Senior woman with lovely girl wearing face mask at park» _builder_version=»4.21.0″ _module_preset=»default» global_colors_info=»{}»][\/et_pb_image][et_pb_button button_url=»@ET-DC@eyJkeW5hbWljIjp0cnVlLCJjb250ZW50IjoicG9zdF9saW5rX3VybF9wYWdlIiwic2V0dGluZ3MiOnsicG9zdF9pZCI6Ijk5OSJ9fQ==@» button_text=»Voksen med CF» button_alignment=»center» _builder_version=»4.21.0″ _dynamic_attributes=»button_url» _module_preset=»default» custom_button=»on» button_text_size=»18px» button_text_color=»#FFFFFF» button_bg_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ button_border_width=»0px» button_border_color=»RGBA(255,255,255,0)» button_border_radius=»69px» button_icon=»||divi||400″ button_icon_color=»#FFFFFF» button_on_hover=»off» custom_margin=»||10px||false|false» custom_padding=»10px|40px|10px|20px|false|false» button_text_shadow_style=»preset1″ locked=»off» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22button_bg_color%22%93}»][\/et_pb_button][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=»4.21.0″ _module_preset=»default» custom_margin=»42px|auto||auto||» custom_margin_tablet=»42px|auto||auto||» custom_margin_phone=»0px|auto||auto|false|false» custom_margin_last_edited=»on|phone» 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″ _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» custom_padding=»|0px||||» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22text_text_color%22%93}»]<\/p>\n
Incidence and Diagnosis
<\/strong>Each year, 8-10 children are born with cystic fibrosis (CF) in Norway, and as of 2018, around 370 people in the country are living with the disease. Diagnosing CF can be a lengthy process involving various tests and may occur at any age. Since 2012, CF has been included in Norway's expanded newborn screening program. The diagnosis relies on genetic testing, sweat tests, and clinical evaluation of symptoms.<\/p>\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» custom_padding=»|0px||||» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22text_text_color%22%93}»]<\/p>\n
Genetics
<\/strong>The CF gene, located on chromosome 7, was discovered in 1989. This gene contains a mutation that leads to cystic fibrosis. It is responsible for producing the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein, which plays a crucial role in regulating salt and water transport across cell membranes in the lungs and digestive system. The mutation impairs the CFTR protein's function, resulting in thick, sticky mucus in the airways and intestines. These areas experience the most severe effects of the disease. As of 2023, over 2,500 genetic variants of the CF gene have been identified, categorized into five classes based on the severity of the disease.<\/p>\n <\/p>\n
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Recent discoveries have identified new mutations that cause milder or atypical forms of cystic fibrosis (CF). As a result, we now differentiate between \"classic cystic fibrosis\" and \"atypical cystic fibrosis.\"<\/p>\n
Atypical CF is a less severe form of the disease linked to mutations in the CFTR gene. Unlike classic CF, individuals with atypical CF often experience mild dysfunction in only one organ system, rather than multiple systems. They may or may not have elevated chloride (salt) levels in their sweat. Atypical CF can vary widely in how it affects different organ systems.<\/p>\n
While our resources primarily cover classic CF, our services are available to everyone with CF, regardless of the form or severity. We plan to provide more information on atypical CF in the future.<\/p>\n
[\/et_pb_toggle][et_pb_toggle title=»Lungekomplikasjon\u202f- seigt sekret og infeksjoner » open_toggle_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ open_toggle_background_color=»RGBA(255,255,255,0)» closed_toggle_background_color=»gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05″ icon_color=»gcid-def3f79a-900d-4425-86b8-efdc1c9633a6″ toggle_icon=»P||divi||400″ use_icon_font_size=»on» icon_font_size=»20px» open_icon_color=»gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05″ open_toggle_icon=»O||divi||400″ open_use_icon_font_size=»on» open_icon_font_size=»20px» _builder_version=»4.21.0″ _module_preset=»default» title_text_color=»#FFFFFF» title_font=»|600|||||||» title_font_size=»18px» title_line_height=»1.4em» body_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ body_link_text_color=»gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05″ custom_margin=»10px||10px||false|false» custom_padding=»||||false|false» border_width_all=»0px» locked=»off» global_colors_info=»{%22gcid-def3f79a-900d-4425-86b8-efdc1c9633a6%22:%91%22icon_color%22%93,%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22open_toggle_text_color%22,%22body_text_color%22%93,%22gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05%22:%91%22open_icon_color%22,%22closed_toggle_background_color%22,%22body_link_text_color%22%93}»]<\/p>\n
The most serious complication of cystic fibrosis (CF) involves the lungs. Due to the defective protein, the mucus in the lungs becomes unusually thick and sticky, making it difficult for the body to clear it effectively. This trapped mucus creates an ideal environment for bacteria to grow, leading to frequent lung infections. These infections require aggressive treatment with antibiotics, guided by microbiological cultures and resistance patterns.\u00a0<\/span>\u00a0<\/span><\/p>\nRepeated or chronic lung infections are particularly dangerous because they cause scarring of the lung tissue and reduce lung capacity over time. For some individuals, the lung damage becomes so severe that a lung transplant is needed for survival. Since 1990, more than 40 people with cystic fibrosis have undergone lung transplantation.<\/span>\u00a0<\/span><\/p>\n[\/et_pb_toggle][et_pb_toggle title=»Tarmene\u202f- viktig med god ern\u00e6ringsstatus » open_toggle_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ open_toggle_background_color=»RGBA(255,255,255,0)» closed_toggle_background_color=»gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05″ icon_color=»gcid-def3f79a-900d-4425-86b8-efdc1c9633a6″ toggle_icon=»P||divi||400″ use_icon_font_size=»on» icon_font_size=»20px» open_icon_color=»gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05″ open_toggle_icon=»O||divi||400″ open_use_icon_font_size=»on» open_icon_font_size=»20px» _builder_version=»4.21.0″ _module_preset=»default» title_text_color=»#FFFFFF» title_font=»|600|||||||» title_font_size=»18px» title_line_height=»1.4em» body_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ body_link_text_color=»gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05″ custom_margin=»10px||10px||false|false» custom_padding=»||||false|false» border_width_all=»0px» locked=»off» global_colors_info=»{%22gcid-def3f79a-900d-4425-86b8-efdc1c9633a6%22:%91%22icon_color%22%93,%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22open_toggle_text_color%22,%22body_text_color%22%93,%22gcid-edcc47c2-e936-4ba2-8e6c-8ca8cb2c2a05%22:%91%22open_icon_color%22,%22closed_toggle_background_color%22,%22body_link_text_color%22%93}»]<\/p>\n
The genetic defect associated with cystic fibrosis (CF) disrupts the absorption of proteins and fats in the intestines, which can make it difficult to maintain weight and height and lead to overall poor health. To address this, many people with CF need to take digestive enzyme supplements with their meals to help their bodies absorb nutrients more effectively. The disease can also lead to CF-related diabetes and liver issues. Therefore, maintaining a proper and balanced diet is crucial for managing CF and ensuring optimal nutritional status.<\/span>\u00a0<\/span><\/p>\n[\/et_pb_toggle][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=»1″ _builder_version=»4.21.0″ _module_preset=»default» custom_padding=»39px||79px|||» global_colors_info=»{}»][et_pb_row column_structure=»1_2,1_2″ _builder_version=»4.21.0″ _module_preset=»default» custom_margin=»0px|auto|23px|auto|false|false» custom_padding=»0px||||false|false» locked=»off» global_colors_info=»{}»][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_font=»Poppins|600|||||||» header_text_color=»gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24″ custom_margin=»0px||0px||false|false» custom_padding=»0px||0px||false|false» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22header_text_color%22%93}»]<\/p>\n
Living with CF<\/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» custom_margin=»||||false|false» global_colors_info=»{%22gcid-26e97d0d-b127-4ce1-b597-0df3fb01df24%22:%91%22text_text_color%22%93}»]<\/p>\n
Dealing with a chronic and serious illness like cystic fibrosis (CF) affects both individuals and their families, and the period around diagnosis can be particularly challenging. CF impacts many areas of life and can sometimes lead to feelings of difficulty, isolation, and loss. However, with proper management and attention to health, people with CF can still experience many of life\u2019s joys, such as traveling, working, and starting a family.<\/p>\n
Har du sp\u00f8rsm\u00e5l eller \u00f8nsker du \u00e5 h\u00f8re andres erfaringer om hvordan de l\u00f8ser sm\u00e5 og store utfordringer med \u00e5 kombinere CF med hverdagen? Bruk v\u00e5re lukkede\u00a0 facebookgrupper, eller ta kontakt med en av v\u00e5re likepersoner som gjerne deler sin erfaring fra \u00e5 leve med eller rundt CF. Medlemskap i gruppene gis etter invitasjon eller ved foresp\u00f8rsel, og du m\u00e5 enten ha CF selv, eller v\u00e6re n\u00e6r p\u00e5r\u00f8rende av noen med CF. Vi oppfordrer alle som blir tatt opp i gruppene til \u00e5 bli medlem i NFCF.<\/p>\n
<\/p>\n
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Informasjon om sykdommenCystisk fibrose er en medf\u00f8dt, alvorlig arvelig multiorgansykdom som skyldes mutasjoner som gir feil i salt- og vanntransporten i kroppens celler. Denne feilen f\u00f8rer blant annet til seigt slim i lungene som skaper grobunn for infeksjoner. Dette p\u00e5virker fremfor alt lungene, bukspyttkjertelen og mage-tarmkanalen. Sykdommen kan gi pustebesv\u00e6r, infeksjoner i lungene og d\u00e5rlig […]<\/p>","protected":false},"author":1,"featured_media":0,"parent":265,"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-270","page","type-page","status-publish","hentry"],"yoast_head":"\n
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