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@sueinmn

Cystic fibrosis and cystic bronchiectasis are completely sepaeeate conditions.

With Cystic bronchiectasis, you need to be aware of any changes in your lung health - congestion, cough, mucus, fatigue, weight loss and and loss of appetite. These are indications of lung infection, which should be diagnosed with a sputum culture to determine which "bug" is invading your lungs.

Cystic fibrosis, on the other hand, is a genetic disorder which is typically diagnosed fairly early in life due to numerous lung infections and digestive issues.

So the caveat here is - if you have a respiratory illness see your pulmonologist ASAP.

How is your breathing and lung function now?
Sue

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Replies to "Cystic fibrosis and cystic bronchiectasis are completely sepaeeate conditions. With Cystic bronchiectasis, you need to be..."

Thanks so much for the information! My CT showed scarring in rt medial lobe and mucoid impaction.
I've had asthma since my teens so I have Albuterol that I use with exercise. I still have lingering cough. I have an appointment in two weeks so hopefully I can get more information. I really appreciate your information!