{"id":46397,"date":"2025-09-27T08:27:11","date_gmt":"2025-09-27T08:27:11","guid":{"rendered":"https:\/\/www.newsbeep.com\/ie\/46397\/"},"modified":"2025-09-27T08:27:11","modified_gmt":"2025-09-27T08:27:11","slug":"im-living-and-loving-after-my-cf-diagnosis","status":"publish","type":"post","link":"https:\/\/www.newsbeep.com\/ie\/46397\/","title":{"rendered":"I\u2019m living and loving after my CF diagnosis"},"content":{"rendered":"<p>I grew up in India, where newborn screening and genetic testing weren\u2019t widely available. For years, I lived in uncertainty, never knowing why my body was failing me. By age 10, I was misdiagnosed with tuberculosis \u2014 a common conclusion in India when constant coughing and <a href=\"https:\/\/www.mayoclinic.org\/symptoms\/coughing-up-blood\/basics\/causes\/sym-20050934\" rel=\"nofollow noopener\" target=\"_blank\">hemoptysis<\/a> appear.<\/p>\n<p>Later, I was also <a href=\"http:\/\/cysticfibrosisnewstoday.com\/cystic-fibrosis-diagnosis\/\" rel=\"nofollow noopener\" target=\"_blank\">diagnosed<\/a> with <a href=\"https:\/\/aafa.org\/asthma\/asthma-triggers-causes\/health-conditions-that-trigger-asthma\/allergic-bronchopulmonary-aspergillosis\/\" rel=\"nofollow noopener\" target=\"_blank\">allergic bronchopulmonary aspergillosis<\/a>, <a href=\"https:\/\/apfed.org\/about-ead\/eosinophilic-asthma\/\" rel=\"nofollow noopener\" target=\"_blank\">eosinophilic asthma<\/a>, and <a href=\"https:\/\/my.clevelandclinic.org\/health\/diseases\/21144-bronchiectasis\" rel=\"nofollow noopener\" target=\"_blank\">bronchiectasis<\/a>, but never with the root cause. <a href=\"http:\/\/cysticfibrosisnewstoday.com\/symptoms-of-cystic-fibrosis\/\" rel=\"nofollow noopener\" target=\"_blank\">Symptoms<\/a> others consider urgent became my normal.<\/p>\n<p>In 2021, I moved to the United States to study biology and pursue a career in healthcare. Within three months, I was hospitalized with an active lung <a href=\"https:\/\/cysticfibrosisnewstoday.com\/upper-respiratory-tract-infections-vs-lower-respiratory-tract-infections\/\" rel=\"nofollow noopener\" target=\"_blank\">infection<\/a>. During rounds in the critical care unit, a pulmonologist suggested <a href=\"https:\/\/cysticfibrosisnewstoday.com\/genetic-testing\/\" rel=\"nofollow noopener\" target=\"_blank\">testing<\/a> for <a href=\"http:\/\/cysticfibrosisnewstoday.com\/cystic-fibrosis-overview\/\" rel=\"nofollow noopener\" target=\"_blank\">cystic fibrosis<\/a> (CF). When the results came back positive, everything shifted. At 19 years old, I finally had an answer: a rare genetic disorder had been shaping my life all along. For the first time, I understood that my suffering wasn\u2019t my fault.<\/p>\n<p>  Recommended Reading<\/p>\n<p>      <img decoding=\"async\" src=\"https:\/\/www.newsbeep.com\/ie\/wp-content\/uploads\/2025\/09\/NewintheNews-150x0-c-default.png\" alt=\"The words \" new=\"\" in=\"\" the=\"\" news=\"\" are=\"\" highlighted=\"\" this=\"\" announcement=\"\" illustration.=\"\"\/><\/p>\n<p>But before that moment of clarity, I\u2019d lived through years of <a href=\"https:\/\/cysticfibrosisnewstoday.com\/columns\/fear-unknown-harder-fighting-disease\/\" rel=\"nofollow noopener\" target=\"_blank\">fear<\/a> and hopelessness. I had attempted to end my life four times. Self-harm had been an addiction since I was just 13, a way to cope with the unexplainable decline of my body. My CF may be considered \u201cmild to moderate\u201d today, but growing up with no diagnosis, deteriorating health, and no hope for answers, I thought about death more than life.<\/p>\n<p>And yet, I survived.<\/p>\n<p>Living a life of meaning<\/p>\n<p>\t\t\t<img fetchpriority=\"high\" decoding=\"async\" class=\"wp-image-97509 size-medium\" src=\"https:\/\/www.newsbeep.com\/ie\/wp-content\/uploads\/2025\/09\/20241218_185155-380x185.jpeg\" alt=\"A woman poses for a photo in front of a river at nighttime. The buildings across the water are lit up and casting reflections on the river's surface.\" width=\"380\" height=\"185\" data-wp-pid=\"97509\"  \/><\/p>\n<p class=\"bio-type-body--small\">Devanshi Dubey visited her home in Kota, Rajasthan, India, in December 2024, but she lives in the United States where she received her CF diagnosis. (Courtesy of Devanshi Dubey)<\/p>\n<p>Today, I\u2019m living the healthiest, happiest life I\u2019ve ever known. 2024 was the year I began not just surviving, but truly living. I went skydiving and completed my longest hike. In 2025, I ran my first 5K and took a two-week solo trip to Boston with no itinerary. These weren\u2019t just milestones; they were proof of a life I once believed impossible.<\/p>\n<p>Now, I live with overwhelming love that sometimes brings me to tears. The thought of having missed this, of never feeling this joy, is unbearable. My family and four closest friends are the reason I\u2019m still here. They give me countless reasons to keep going, and because of them, I get to give all the love I once thought I\u2019d never have the chance to share.<\/p>\n<p>I dream of running a marathon, publishing the book I\u2019ve started writing, and advocating for global access to <a href=\"http:\/\/cysticfibrosisnewstoday.com\/cystic-fibrosis-treatment\/\" rel=\"nofollow noopener\" target=\"_blank\">CF treatments<\/a> and true equity in healthcare. I don\u2019t want to \u201cchange the world\u201d in the abstract sense. I want to change the world for the people I meet \u2014 the ones who cross my path, even briefly. I want them to feel seen, safe, and inspired simply through how I choose to live.<\/p>\n<p>Because today, <a href=\"https:\/\/cysticfibrosisnewstoday.com\/living-with-cystic-fibrosis-2\/\" rel=\"nofollow noopener\" target=\"_blank\">I am living<\/a>. And I refuse to take a single breath for granted. Having lived what many call an \u201cextraordinary\u201d life, even the smallest moments and victories feel rich and almost unreal.<\/p>\n<p>But sometimes I wonder if maybe I\u2019m just too sensitive, if I take life too seriously. I\u2019ve often been told, \u201cDon\u2019t overthink,\u201d or \u201cJust ignore it.\u201d But how do you ignore something that shapes every part of your existence? How do you stop thinking about the one thing that has dictated everything you could or couldn\u2019t do?<\/p>\n<p>Growing up, my world was consumed by managing my health and keeping up with school. I tried many things \u2014 dancing, tae kwon do, and other hobbies \u2014 but I always had to quit. I\u2019ve tried almost every activity, but my body never allowed me to master any one skill. I became good at things that didn\u2019t demand physical strength, which I\u2019m proud of, but I still feel the weight of everything I couldn\u2019t do.<\/p>\n<p>I never had time to pursue passions fully. I can\u2019t swim to save my life, and I\u2019ve missed out on so many simple experiences that help people connect and socialize, all because sickness filled the space where childhood, hobbies, and skills should have been.<\/p>\n<p>Now that I\u2019m healthier than ever, I\u2019m finally chasing the things I once thought I\u2019d never get to do. The road is long, but I\u2019m learning to be patient with myself. Along the way, I\u2019ve realized that everyone is on their own journey, moving at their own pace. Our paths may not always cross, and that\u2019s OK. What matters is that I\u2019m finally walking mine.<\/p>\n<p>And yet, I often come across people who are not on the same wavelength as me \u2014 people who don\u2019t take life as seriously, who cannot keep up with the intensity I live with. I\u2019m drawn to those who carry the same fire, the same zest for life and love that I do. People who want to live with meaning and wake up each morning determined to do so.<\/p>\n<p>Today, I live each day aware of every breath, every moment. I live a life of meaning, love, and purpose, and I know that\u2019s enough to change the world.<\/p>\n<p>To submit your own Guest Voice for publication on <a href=\"https:\/\/cysticfibrosisnewstoday.com\/\" rel=\"nofollow noopener\" target=\"_blank\">Cystic Fibrosis News Today<\/a>, please email your idea to our columns manager at <a href=\"http:\/\/cysticfibrosisnewstoday.com\/cdn-cgi\/l\/email-protection#650d040916001c4b07090a060d001725070c0a0b0012164b060a08\" rel=\"nofollow noopener\" target=\"_blank\">[email\u00a0protected]<\/a> with the following included in the subject line: \u201cGuest Voice: Cystic Fibrosis News Today.\u201d<\/p>\n<p>Note: Cystic Fibrosis News Today\u00a0is strictly a news and information website about the disease. It does not provide medical advice,\u00a0diagnosis, or\u00a0treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of\u00a0Cystic Fibrosis News Today\u00a0or its parent company, Bionews, and are intended to spark discussion about issues pertaining to cystic fibrosis.<\/p>\n","protected":false},"excerpt":{"rendered":"I grew up in India, where newborn screening and genetic testing weren\u2019t widely available. For years, I lived&hellip;\n","protected":false},"author":2,"featured_media":46398,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[34],"tags":[103,397,396,61,60],"class_list":{"0":"post-46397","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-healthcare","8":"tag-health","9":"tag-health-care","10":"tag-healthcare","11":"tag-ie","12":"tag-ireland"},"_links":{"self":[{"href":"https:\/\/www.newsbeep.com\/ie\/wp-json\/wp\/v2\/posts\/46397","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.newsbeep.com\/ie\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.newsbeep.com\/ie\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/ie\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/ie\/wp-json\/wp\/v2\/comments?post=46397"}],"version-history":[{"count":0,"href":"https:\/\/www.newsbeep.com\/ie\/wp-json\/wp\/v2\/posts\/46397\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/ie\/wp-json\/wp\/v2\/media\/46398"}],"wp:attachment":[{"href":"https:\/\/www.newsbeep.com\/ie\/wp-json\/wp\/v2\/media?parent=46397"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.newsbeep.com\/ie\/wp-json\/wp\/v2\/categories?post=46397"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.newsbeep.com\/ie\/wp-json\/wp\/v2\/tags?post=46397"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}