lightNlife
New member
Hi Nonnie,
Although most of what you hear about cystic fibrosis is that it affects the lungs, the truth is it affects the entire exocrine system. The thick, sticky mucus that gets stuck in our airways and makes it hard for us to breathe, also causes problems in our intestines and pancreas and can affect how well (if at all) we absorb the food we eat. Every body system is affected in some way by cystic fibrosis. There is nothing this disease leaves untouched. Some people are fortunate to enjoy long stretches of relatively mild symptoms, but since the disease is progressive, there comes a point when the body is simply over-taken and worn out.
If you'd like to learn more about cystic fibrosis, I have written several articles about the different aspects of it. Just click on this link: <a target=_blank class=ftalternatingbarlinklarge href="http://www.associatedcontent.com/user/28077/lauren_beyenhof.html
">http://www.associatedcontent.c.../lauren_beyenhof.html
</a>
Be warned that this is a lot of heavy duty information, and with everyone's specific set of symptoms, there's a lot of difference. Some people have only mild digestive problems, others may die young from complications of a bowel obstruction. As doctors and researchers learn more, there are new treatments that are becoming available to us that may help us live longer, more productive lives. And perhaps one day, a cure will be found.
If you find yourself overwhelmed or becoming emotional about all it involves, just take a step back and let it sink in. If your sister-in-law is willing to discuss CF with you, (and perhaps she's very private about CF) maybe ask her what things she does each day to help fight the symptoms of CF. She may not want to talk, and that's okay. At least you'll have learned enough from this site to be someone who is a least a little bit familiar with CF.
Happy "snooping". <img src="i/expressions/face-icon-small-smile.gif" border="0">
Although most of what you hear about cystic fibrosis is that it affects the lungs, the truth is it affects the entire exocrine system. The thick, sticky mucus that gets stuck in our airways and makes it hard for us to breathe, also causes problems in our intestines and pancreas and can affect how well (if at all) we absorb the food we eat. Every body system is affected in some way by cystic fibrosis. There is nothing this disease leaves untouched. Some people are fortunate to enjoy long stretches of relatively mild symptoms, but since the disease is progressive, there comes a point when the body is simply over-taken and worn out.
If you'd like to learn more about cystic fibrosis, I have written several articles about the different aspects of it. Just click on this link: <a target=_blank class=ftalternatingbarlinklarge href="http://www.associatedcontent.com/user/28077/lauren_beyenhof.html
">http://www.associatedcontent.c.../lauren_beyenhof.html
</a>
Be warned that this is a lot of heavy duty information, and with everyone's specific set of symptoms, there's a lot of difference. Some people have only mild digestive problems, others may die young from complications of a bowel obstruction. As doctors and researchers learn more, there are new treatments that are becoming available to us that may help us live longer, more productive lives. And perhaps one day, a cure will be found.
If you find yourself overwhelmed or becoming emotional about all it involves, just take a step back and let it sink in. If your sister-in-law is willing to discuss CF with you, (and perhaps she's very private about CF) maybe ask her what things she does each day to help fight the symptoms of CF. She may not want to talk, and that's okay. At least you'll have learned enough from this site to be someone who is a least a little bit familiar with CF.
Happy "snooping". <img src="i/expressions/face-icon-small-smile.gif" border="0">