← Return to Bronchiectasis: Is nebulizing helpful?
DiscussionBronchiectasis: Is nebulizing helpful?
MAC & Bronchiectasis | Last Active: Oct 21, 2021 | Replies (76)Comment receiving replies
Replies to "Thanks to everyone for their humour and support when it comes to living with bronchiectasis and..."
That's wonderful, Kathy. Thank you for sharing that! Can you briefly share your other lifestyle and dietary changes? Was it gluten free changes?
Very interesting to me because as I have posted in the past, my pulmonologist doesn't believe nebulizing is necessary. He stated as long as I use my inhaler prior to doing my smart vest, I will get the same results. I'm having a problem with this mindset. Any input from those who may have dealt with the same thinking from their doctor?? Thank you !! Toni
I have been following this discussion for many months & appreciate all who post. I was quickly diagnosed nearly 4 yrs ago with bronchiectasis & MAC. My symptoms have been mild with the exception of hemoptysis which originally led me to the ER & later to the brink of the “big 3”. My pulmonologist suggested nebulizing 3% sodium chloride about 16 months ago which I did faithfully. My hemoptysis continued with incidents occurring more often. In February after discussion with my pulmonologist, I started mixing 3% & 7% & eventually was able to easily tolerate 7%. When I saw my pulmonary Dr. in April, she recommended treatment with the big 3 as my hemoptysis continued every few weeks. At her referral, I also saw an infectious disease Dr. & he did not believe my symptoms warranted antibiotic treatment. I told them both that I expected to cough up blood or clots in the next day or two, but otherwise I had no challenging symptoms (ha?). That was nearly 3 months ago. I believe the 7% sodium chloride has made the difference & I owe its use to all of you who share your wisdom & experience.
Great news! How do you feel compared to a yar ago?
Sue