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@songfeijun

I have yet to see a pulmonologist next week and an ID next week too. I am not sure I will go with bronchoscopy and lung wash even if they suggest so for just a "firm diagnosis of MAC", unless they have other strong arguments to do that.

my thinking is that if they can for sure confirm the MAC with all the details, I will just leave it with neb saline to control it. I will come back next week on the doctor visit. Thanks.

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Replies to "I have yet to see a pulmonologist next week and an ID next week too. I..."

I agree with @bee1950. I've coughed up about 2-3 TBS blood twice over the past 4 years (a combination of red blood and clots). The first time, I went to the ER and that, eventually, led (after about 1 ½ yrs) to the diagnosis of bronchiectasis and MAC. I cough in the mornings, but don’t really have any other symptoms and don’t take any antibiotics. I exercise/walk 2-3 miles daily and nebulize 7% saline. I've been investigating whether coughing up blood may actually be a good thing in MAC. In my reading of MAC articles, I found one called "Retrospective study of the predictors of mortality and radiographic deterioration in 782 patients with nodular/brochiectatic MAC lung disease" by Gochi et al. ( https://www.ncbi.nlm.nih.gov/pubmed/26246077 ) From the article, very few people seemed to die of MAC-related issues. The women with bloody sputum fared the best. I'm trying to find out why.

Hi! Just wanted to throw out there that my pulmonologist felt I had MAC (and bronchiectasis) from my CT scan. I did have a bronchoscopy ( isn't bad at all ) and did not have MAC in any of my tests. Was glad that the results of MAC did not show up in the biopsy/washings. From this forum began using the 7% saline and basically have been "healthy" ever since I received the bronchiectasis diagnosis.