{"id":11324,"date":"2024-05-15T10:45:41","date_gmt":"2024-05-15T10:45:41","guid":{"rendered":"https:\/\/jamaicahospital.org\/newsletter\/?p=11324"},"modified":"2024-05-15T10:45:41","modified_gmt":"2024-05-15T10:45:41","slug":"cystic-fibrosis-awareness-month","status":"publish","type":"post","link":"https:\/\/jamaicahospital.org\/newsletter\/cystic-fibrosis-awareness-month\/","title":{"rendered":"Cystic Fibrosis Awareness Month"},"content":{"rendered":"<p><span style=\"font-weight: 400\"><a href=\"https:\/\/jamaicahospital.org\/newsletter\/wp-content\/uploads\/2024\/05\/GettyImages-1082582778.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-11325 alignright\" src=\"https:\/\/jamaicahospital.org\/newsletter\/wp-content\/uploads\/2024\/05\/GettyImages-1082582778-300x200.jpg\" alt=\"A child being tested for cystic fibrosis.\" width=\"344\" height=\"234\" \/><\/a>May is Cystic Fibrosis Awareness Month. During this time, Jamaica Hospital Medical Center is working to provide important information about this disease for our patients, including its symptoms, potential complications, and current available treatments.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400\">Cystic fibrosis (CF) is a hereditary disease that affects the mucus-producing cells in your body.\u00a0 CF occurs when there is a mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This mutation disables cells from moving chloride (a component of salt) to their surfaces. Without the movement of chloride, cells cannot hydrate properly, causing your body to produce thicker, stickier mucus.<\/span><\/p>\n<p><span style=\"font-weight: 400\">The buildup of heavy mucus caused by CF can damage the digestive system, lungs, and other organs that depend on mucus to function by obstructing the ducts, tubes or passageways of these organs. Those living with cystic fibrosis also often have abnormally high levels of salt in their sweat. Other symptoms that may develop as a result of the disease include:<\/span><\/p>\n<ul>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Frequent lung infections, such as recurrent pneumonia or bronchitis<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Persistent cough with thick mucus<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Frequent sinus infections<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Wheezing<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Shortness of breath<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Nasal polyps<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Fatigue<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Delayed growth or puberty<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Bowel movements that produce greasy, bulky stool<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Severe constipation<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Male infertility<\/span><\/li>\n<\/ul>\n<p><span style=\"font-weight: 400\">All babies born in the United States are screened for cystic fibrosis by testing small blood samples. If someone is suspected to have CF, their doctor can also order a sweat test to determine if their chloride levels are normal.<\/span><\/p>\n<p><span style=\"font-weight: 400\">Currently, there is no cure for CF; treatment generally focuses on alleviating symptoms and reducing complications. Treatment may include:\u00a0<\/span><\/p>\n<ul>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Medications, such as antibiotics for lung infections, anti-inflammatory medications, stool softeners, mucus-thinning drugs, medications that assist in nutrient absorption, and medications that treat gene mutations<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Physical therapy<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Pulmonary rehabilitation<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Surgery<\/span><\/li>\n<\/ul>\n<p><span style=\"font-weight: 400\">To learn more about cystic fibrosis or to make an appointment with a <\/span><a href=\"https:\/\/jamaicahospital.org\/clinical-services\/pulmonary-medicine\/\"><span style=\"font-weight: 400\">pulmonologist<\/span><\/a><span style=\"font-weight: 400\"> at Jamaica Hospital Medical Center, please call (718) 206-7126.<\/span><\/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>May is Cystic Fibrosis Awareness Month. During this time, Jamaica Hospital Medical Center is working to provide important information about this disease for our patients, including its symptoms, potential complications, and current available treatments.\u00a0 Cystic fibrosis (CF) is a hereditary &hellip; <a href=\"https:\/\/jamaicahospital.org\/newsletter\/cystic-fibrosis-awareness-month\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":42,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[1611,2063],"class_list":["post-11324","post","type-post","status-publish","format-standard","hentry","category-health","tag-cystic-fibrosis","tag-cystic-fibrosis-awareness-month"],"_links":{"self":[{"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/posts\/11324","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\/42"}],"replies":[{"embeddable":true,"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/comments?post=11324"}],"version-history":[{"count":1,"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/posts\/11324\/revisions"}],"predecessor-version":[{"id":11326,"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/posts\/11324\/revisions\/11326"}],"wp:attachment":[{"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/media?parent=11324"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/categories?post=11324"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/jamaicahospital.org\/newsletter\/wp-json\/wp\/v2\/tags?post=11324"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}