Aspergillus with MAC
Has anyone else picked up aspergillus (pulmonary fungal infection) while being treated for MAC? MY ID doc has it on watch because it can't be treated while I am being treated for the MAC, due to drug interactions. It doesn't help that my local clinic threw out my last two culture specimens for fungus because there was not enough for AFB cultures even though I wrote on big Sharpie twice on the second one was for fungus. I also have colonized pseudomonas, and am not currently being treated for that.
If you do have this situation, how has your doc been handling it?
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
My answer above got cut off, I see. My cat must have been helping me type.
@windwalker we appreciate you!
@windwalker I know you can do this and get better again, I will look forward to it.
I also have a CF gene. I was diagnosed with Bronchiectasis, nocardia and Mac in 2003 at National Jewish Research Center. I was on the three meds for a year. Then was treated with bactram for a year for the nocardia. Been treated off and on thru the years for Nocardia. I finished another year on bactram about 6 months ago and have just recently been diagnosed with Mac again. So I’m back on the big 3 meds. I seem to tolerate the meds ok - just getting tired of always being on ‘something’. Sure glad I found this site . It does help to read and compare - especially how we all react to the meds. What works and what doesn’t.
@windwalker - I second this -- your positive attitude and knowledge and assistance have gotten me through my journey with my positive attitude in place -- thank you!
@marilynk I am sick of being of meds too, however think im in it for the long haul!
Just had to add cipro to the mix as doc thinks t may have pseudomonas-started coughing blood and yellow sputum. Just three doses and doing better already so that’s encouraging.
@glendamoseley did you get the chart?
@glendamoseley, can you see this post with the saline chart? Click on the blue highlighted conversation above and the chart will open.
Thanks for this article. I see that a number of people are using 7% saline in their nebulizer but the doctors I have seen have only recommended 3%. Would be interested in comments on this. Also for brigby, there are devices that can help you clear your airways more easily, even if you have limited pulmonary function and also medications to help liquefy sputum and clear your lungs. I wonder whether you were able to discuss this with your doctor?