OMG! Reading your post, I might have thought you were talking about me. When they told me back in August that the reason 3 months of IVs didn't work was because I had an infection that was "very difficult to treat". That being aspergillus. I seriously had NEVER heard of that, I was completely dumbfounded and depressed. I was admitted to hospital again, and treated with antibiotics, improved, but only for a short while. My IGE levels suggested that I may allergic to aspergillus (ABPA), but they did skin allergy tests that suggested I (mildly) was. Still, they believe that other combined factors suggest an ABPA diagnosis. I have since started taking anti-fungals, and am dreading the prednisone that may follow. All I know is I feel worse than ever in my life, the onset seemed quite quick (I went from 80% Fev1 to 35% in a matter of months), and it is affecting me tremendously. I, like you, cough till I feel my eyes might bulge out, I can't eat, I'm nauseous. And, I can not seem to get much info from the "experts". Can you tell I'm bitter? I would love to hear from you and hear how you are doing.
Kelly