I saw my GP today. Struggling for breath, wheezing etc. I'd started my rescue pack and had both steroids and amoxicillin bust hadn't felt either worked. Now I've been diagnosed for 5.5 years with bronchiectasis (and sarcoidosis) but as I was saying to my GP I have no idea why it is like to have bronchiectasis. I rarely cough, when I do it's dry. Phlegm is almost non-existent. My lungs feel dry ( that might be the PF). So my question is, does this description resonate with fellow bronchiectasis sufferers? Or should I speak to my consultant?