New to MAC and considering treatments options: What did you do?
Hi all,
I started getting chest pains and breathing difficulties early May and after much testing and a biopsy, I was diagnosed with MAC. My doctor did not give me much information. He only told me that my symptoms were not severe enough for treatment and just said we would get a chest x-ray once a year to monitor it. Is that normal? Unfortunately, this was a phone call and he was in a rush to hang up and did not seem to want to answer my questions (I had to ask him to stay on the phone and then asked if this is just a chronic thing I will have now or if it will go away eventually and was told "I don't have a crystal ball.") He gave me zero resources and no recommendations for what to do/avoid. Is there a good place I can learn about this? I only see stuff about the year plus of three antibiotics which he said we don't need to do right now and nothing about day to day life. Is there something I can do to make sure it doesn't get worse/slow its progress? Any direction would help. Thanks!
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Hi! I was recent diagnosed in April with MAC after living with mild Bronchiectasis since 2018.
I started treatment with the Big 3 in June. However, treatment isn’t necessarily as bad as symptoms even though I read the same things. After 2 months, I feel 50% better than I did before. Mind you, the side effects produce some of the same symptoms as the disease -but for me, on a smaller scale and more tolerable. You should definitely sign up for the virtual seminar sent by men 08. You can sign up by listing yourself under education speciality. This worked for me and someone emailed me directly concerning attendance. My best piece of advice// Get educated on your disease!! The medical community is just not well versed in this and you have to be your own health advocate. Really hope this helps!
What are the big 3 specifically?
Either azithromycin (Zithromax) OR clarithromycin (Biaxin),
Ethambutol (Myambutol), &
Rifampin (Rifadin, Rimactane)
They thought my MAC was from silent aspiration. Coincidentally, I too have choking episodes, even on my own spit. I was referred to GI dr. They did 24 hr monitoring with impedance, Manometry and EGD. Results were good, except I have Ineffective esophageal motility. My sister, mother, cousin, etc have. I just make sure I chew food very well and always have water when eating.
Can you list the specific meds. Thank you.
Someone recently posted a tincture they use that helps with symptoms. I can’t find post. I think it was maybe echinacea and something. Anyone remember?
Thank you
Are all protocols different. Do you take iv antibiotics or orally. Are they taken all at once or alternate?
I was on Azithromycin, Ethambutol, Rifampin - Mon/Wed/Fri. This regimen didn't result in sputum conversion (except for one month), so I am now on them daily and also just started Arikayce. So far, Arikayce has resulted in hoarse voice, no other side effects to report.
Thank you!