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New to Mycobacterium Gordonae HELP needed

MAC & Bronchiectasis | Last Active: Apr 16, 2019 | Replies (19)

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@sueinmn

Has anyone else had this experience? I have had MAC and been under treatment since July 2018, the past 3 months taking the meds daily due to persistent positive cultures and evidence of growing spots on my latest CT. Now the past two cultures, in June and September, have grown both MAC and M Gordonae. The current plan is to repeat culture and CT in December and see my ID doc then.
What questions should I be asking? Is there a doc anywhere with experience with M gordonae?

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Replies to "Has anyone else had this experience? I have had MAC and been under treatment since July..."

Sorry that you have this new concern. M gordonae is common in tap water- I isolated some from a faucet in NYC when I had water tested, but it does not usually cause disease unless you have a compromised immune system. It could also be a contaminant in the culture although that seems less likely if found twice in succession, but anyhow, your ongoing MAC is a greater concern and if the gordonae is truly present should respond to the same treamtnets
I expect the ID doctor will be more focused on whether your MAC is showing any response to the daily meds and might want to tweak treatment. If you have not already had drug sensitivity testing on your MAC strain or found out the exact species, this might be a good time to do it to make informed treatment decisions

@sueinmn Hi Sue. Man, it stinks to learn that other 'bugs' take up residence in our lungs. It is not uncommon to pick up additional infections from various bacterias when you have mac and/or bronchiectasis. The same issue at hand that allowed mac to become an infection; holds true for other mycobacterias. I caught pseudomonas while into my third year on antibiotics. Fortunately, switching one of my antibiotics out and adding tobramycin got rid of it in 30 days. Mind you, I am still on maintenance meds to keep it away. That will be a good discussion for your I.D. dr. on whether it needs to be treated. Please keep me posted on what treatment path, if any; they put you on.

Thanks for the responses. Yes, they have identified exact species and done sensitivity testing - switched from clarithromycin to azithromycin many months ago because it showed better response. Doc is trying to hold tobramycin "in reserve" but we talked this week and he is getting closer to trying it if next CT doesn't show improvement and next sputum samples are still positive. I am truly getting frustrated, so it's great to hear from people here. I took a 30 minute medium paced walk this morning and was pleased that I could talk to my friend as we walked - 3 months ago that was impossible. Does anyone have a feeling for how much of my fatigue is MAC, and how much is these infernal antibiotics?