← Return to Bronchiectasis: New Diagnosis
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Replies to "Hi Carol. I was diagnosed with MAC and Pseudomonous early 2019 after bronchoscopy. Local pulmonary doc..."
@marellen. Sorry I could not finish my post this morning. When the pulmonary doc. said "You may just have to live with it" I was stunned and afraid. Also wanted to mention that he nor his staff ever gave me a single piece of literature about this disease or possible treatment. It so happens my sister in law is a retired nurse at Mayo in MN. In talking with her she knew about Mayo Connect and suggested that I get on line with the group to see it there was anything I could learn there. I read posts for a couple of days and then decided to post my experience to that point. Within a couple of days a woman in the Birmingham area sent me a message saying she had a similar experience with a doctor in Birmingham. She started reaching out and found a doctor in Atlanta. She had seen him twice and was extremely pleased with him. She shared his contact information with me. I felt I needed to try to get an appt. with this doctor. I called in August and they said it would be February before I could see him. OK, I'll try and live till then. Now here is where God took over. (He was really at work before that.) Anyway, the doctors office called me in just a few days and said, "Can you come Friday." Wow, you bet I can. I'm getting too wordy but it has been such an experience. I went to Atlanta and when I left I was walking on air. This doctor knew what he was doing. He said I probably should not have been on medication at all. I walked out of his office with a nebulizer and a prescription for 3% Sodium Chloride and a lot of printed literature. My first sputum to him grew out Pseudomonas (multiple colonies). I had to have a PICC line in place for 2 weeks and nebulize Tobramycin for 28 days. That cleared things for a period of months. I again tested positive for Pseudomonas in February 2020 but not as severe as last September and I'm finishing up another round of Tobramycin this next week. I will then send in more sputum to see if it is gone. Dealing with this disease at times is tiring, frustrating and mystifying. Don't be afraid of getting another opinion. I have learned so much from this group--thank God for each and every one of these wonderful folks who step up and share. Because of reading about the difference between 3% and 7% Sod. Chloride I contacted my doctor and asked if he would change my prescription--he did. OK, I gone through all I could think of and hope it was hopeful. We must be brave and advocate for ourselves through this journey we're on. May God bless you.
Faye
@fdixon63 I would be very interested in “what happened next.” irene5