I have a disease called Cystic Fibrosis or (CF). Cystic Fibrosis is a life-limiting disease that affects the lungs and digestive system. Thick, sticky mucus builds up in my lungs, pancreas, and other vital organs of my body. On the outside, I look like an average college student, but behind the scenes, there are many things I have to do to maintain my health. I do daily treatments consisting of inhaled medications and airway clearance, as well as take a variety of medications and supplements in order to improve the absorption of calories and vital nutrients --all of which are done just when I am healthy!
The life expectancy of CF is in the mid to late forty’s. I do many activities, and I do not let this limit my capabilities or life goals. I plan to have a very successful career, have a family, and live my life to the fullest. Many of you may be reading this and wondering why I am sharing this with a blog. This blog is all about my professional and personal life. Cf is one small part of who I am but not all of me. There have been many great opportunities that have come from this diagnosis. I can use all of my tools to help others not only in the cf community but others around me. If you ever have any questions feel free to ask, I am open and happy to educate my peers and others around me.
The life expectancy of CF is in the mid to late forty’s. I do many activities, and I do not let this limit my capabilities or life goals. I plan to have a very successful career, have a family, and live my life to the fullest. Many of you may be reading this and wondering why I am sharing this with a blog. This blog is all about my professional and personal life. Cf is one small part of who I am but not all of me. There have been many great opportunities that have come from this diagnosis. I can use all of my tools to help others not only in the cf community but others around me. If you ever have any questions feel free to ask, I am open and happy to educate my peers and others around me.
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