{"id":6398,"date":"2019-04-09T20:58:09","date_gmt":"2019-04-09T20:58:09","guid":{"rendered":"http:\/\/jamaicahospital.org\/newsletter\/?p=6398"},"modified":"2019-04-09T21:07:20","modified_gmt":"2019-04-09T21:07:20","slug":"learn-the-facts-about-cystic-fibrosis","status":"publish","type":"post","link":"https:\/\/jamaicahospital.org\/newsletter\/learn-the-facts-about-cystic-fibrosis\/","title":{"rendered":"Learn The Facts About Cystic Fibrosis"},"content":{"rendered":"<p>Cystic fibrosis (CF) is a hereditary disease that affects the cells in your body that make mucus. \u00a0CF occurs when there is a mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The mutation disables cells from moving chloride (a component of salt) to their surfaces.\u00a0 Without the movement of chloride, cells cannot hydrate properly. \u00a0This leads to the production of mucus that is thicker and stickier than normal.<a href=\"http:\/\/jamaicahospital.org\/newsletter\/wp-content\/uploads\/2019\/04\/cystic-fibrosis-538052760.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-6399 alignright\" src=\"http:\/\/jamaicahospital.org\/newsletter\/wp-content\/uploads\/2019\/04\/cystic-fibrosis-538052760.jpg\" alt=\"\" width=\"309\" height=\"208\" \/><\/a><\/p>\n<p>CF can result in damage to the digestive system, lungs, and other organs that utilize mucus to function.\u00a0 The buildup of mucus can obstruct the ducts, tubes or passageways of these organs.<\/p>\n<p>Those living with cystic fibrosis often have abnormally high levels of salt in their sweat. \u00a0Other complications or symptoms that may develop as a result of the disease include:<\/p>\n<ul>\n<li>Frequent lung infections, including recurrent\u00a0 pneumonia or bronchitis<\/li>\n<li>Persistent cough with thick mucus<\/li>\n<li>Frequent sinus infections<\/li>\n<li>Wheezing<\/li>\n<li>Shortness of breath<\/li>\n<li>Nasal polyps<\/li>\n<li>Fatigue<\/li>\n<li>Delayed growth or puberty<\/li>\n<li>Poor weight gain<\/li>\n<li>Bowel movements of greasy bulky stools<\/li>\n<li>Severe constipation<\/li>\n<li>Male infertility<\/li>\n<\/ul>\n<p>All babies born in the United States are screened for cystic fibrosis by testing small blood samples. In other cases, if someone is suspected to have CF, their doctor can order a sweat test to determine if chloride levels are normal.<\/p>\n<p>Currently, there is no cure for CF. However; treatment is focused on alleviating symptoms and reducing complications. Treatment may include medications, physical therapy, pulmonary rehabilitation or surgery.<\/p>\n<p>To learn more about cystic fibrosis or to make an appointment with a pulmonologist at Jamaica Hospital Medical Center, please call\u00a0\u00a0 718 206 7126.<\/p>\n<p>&nbsp;<\/p>\n<p class=\"disclaimer\">All content of this newsletter is intended for general information purposes only and is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment.  Please consult a medical professional before adopting any of the suggestions on this page.   You must never disregard professional medical advice or delay seeking medical treatment based upon any content of this newsletter.<strong>  PROMPTLY CONSULT YOUR PHYSICIAN OR CALL 911 IF YOU BELIEVE YOU HAVE A MEDICAL EMERGENCY.<\/strong> <\/p>","protected":false},"excerpt":{"rendered":"<p>Cystic fibrosis (CF) is a hereditary disease that affects the cells in your body that make mucus. \u00a0CF occurs when there is a mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The mutation disables cells from moving chloride &hellip; <a href=\"https:\/\/jamaicahospital.org\/newsletter\/learn-the-facts-about-cystic-fibrosis\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[12],"tags":[1611],"class_list":["post-6398","post","type-post","status-publish","format-standard","hentry","category-pulmonary-medicine","tag-cystic-fibrosis"],"_links":{"self":[{"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/posts\/6398","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/users\/8"}],"replies":[{"embeddable":true,"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/comments?post=6398"}],"version-history":[{"count":3,"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/posts\/6398\/revisions"}],"predecessor-version":[{"id":6402,"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/posts\/6398\/revisions\/6402"}],"wp:attachment":[{"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/media?parent=6398"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/categories?post=6398"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/tags?post=6398"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}