← Return to Tell us how you "Live Life Fully" with Bronchiectasis and MAC
DiscussionTell us how you "Live Life Fully" with Bronchiectasis and MAC
MAC & Bronchiectasis | Last Active: Jun 27 7:01pm | Replies (55)Comment receiving replies
Replies to "@annagh Interesting to me. You were diagnosed in 2015 with BE and in 2022 with MAC...."
@blm1007blm1007
My primary care doctor made the bronchiectasis diagnosis after several bouts of walking pnemonia. It took a while to get to a pulmonologist as I was in the process of relocating. He suspected MAC (2017), but I didn’t yet know how to get a good sputum sample and he opted not to do a bronchoscopy, saying my CT Scan actually showed some improvement, and he’d rather not treat me due to the potential side effects of the drugs. Unfortunately, he didn’t offer nebulizing or airway clearance and I basically lived with the cough. It was H-influenza that finally made me sick enough, that the broncoscopy revealed MAC. From you posts I see that you are very diligent about investigations and self-care, which is admirable. Good for you! We each have our own comfort levels and ways of achieving them
Anna.
Connect

@blm1007blm1007 I saw this on this site a couple of years ago. It should help clear the lungs properly. Watch till the end as the doctor recommends the cheaper version of these methods.