← Return to A-Fib and MAC

Discussion

A-Fib and MAC

MAC & Bronchiectasis | Last Active: Jan 10, 2022 | Replies (41)

Comment receiving replies
@anonymous217382

Dear Sounder27, You Just imparted some great knowledge my way!!! Thank-you. I will surely pass along any information too. My Infectious Disease doctor was not in today, so will know tomorrow why I was never tested for MAC. As for the Pulmonologist, after the Bronchoscopy, he never answers calls. It is really weird, like what happened? It is always an answering machine, so I left a message kindly asking if he could test me for MAC. No response. Guess it is time to find a human-being for a Pulmonologist!

Jump to this post


Replies to "Dear Sounder27, You Just imparted some great knowledge my way!!! Thank-you. I will surely pass along..."

Connie, your experience with a response-phobic Pulmo reminds me of my experience with two Pulmos. Although I like them both the first one arranged for me to get a percussion vest, and concurrently started me nebulizing 0.09% saline. At that time I hadn't discovered the Mayo Connect Treasure Trove of useful treatment info for our maladies. The Pulmo didn't mention that 0.09 is but one of multiple saline concentrations and I was too dumb to question his choice.
After he bailed out of his practice I transferred to his office colleague who continued on the same regimen for months and months, up until the time I mentioned to him that I had learned of the availability of a 7% solution which was reputed to kill or at least make life miserable for MAC infections. He gave no indication that he had ever heard that good news, but happily complied with my request to amp up my saline Rx to 7%. And I've lived happily ever after...sorta. Don