Extreme fatigue with MAC
Good Morning, I am new here so this may have been discussed before. I was diagnosed with MAC in 2012 after I was diagnosed with breast cancer. I had a biopsy and lung wedge resection...both confirmed the MAC. In 2015 I had a bronchoscope done which again confirmed the MAC and bronchiectasis. I have seen a Pulmonologist, infectious disease and my primary care doctor. Everyone seems up in the air whether to treat or not. They seem to be leaving the decision up to me. I don't have a cough, I do have some shortness of breath occasionally but I am always tired. No matter how much I rest or sleep.....I am tired and sometimes exhausted after minor activity. Is fatigue a main symptom of the disease. Would treatment help my fatigue or make is worse. Thank you!
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What pills were these?
The one that effect my hearing was azithromycin.Luckily when I stopped it my hearing came back. I am now on Etibi ,Rofact and moxifloxacin I think I will be changing the moxifloxacin as it was recently on the news about how it can cause problems with the aorta .
Just checking to see if I can get in.
Jane,
Im so sorry to hear of all your going through. I can tell you of my experience with MAC that the exhaustion has had serious bouts to the point of barely wanting to or being able to move. My last bout of it I went off the big 3 as prescribed and it seemed to stop the cycle. I think only a pulmy with experience in MAC could tell you whether to get treated. I have a feeling its the meds that cause the fatigue .I could be wrong. ONly the truth is the meds are very strong and everyone has there ways of adapting/ or not, biologically that is. For me I think the meds cause the fatigue only if I get the flu and Im not on the meds I dont pick up again and usually its a sign that the bacteria are still lurking around. The other thing that helps with the fatigue is finding just the right balance of exercise and good solid rest are I think top priorities in steering clear of possible problematic side effects.
I hope you are under good care that you trust and keep up the work, its worth every moment.
Deborah
I was told there is the possibility that you can get over it on your own. My guess would be that would only be the case if a person had a mild case....but it’s just a guess. Is this not true?
What are the usual symptoms of bronchiectasis?
I went to their web page and found it to be confusing. I didn’t see anything about treating MAC. I must have navigated wrong???. And I did not see how you can get to see someone.... somehow it looked to me like it was all research.
@debminuet The meds knocked me out also for around 18mths then I adjusted a bit, still tired but able to do more, pretty bad, but worth it to this point. Take care
@sylvermoon8 I looked up NIH, and I guess they are strictly research. Not sure if they take patients in like Mayo does. They do have a number for patients wanting to be included in research. I received successful treatment at Mayo Clinic; but I know that they use my medical records for their research. Here is the number for patient intake at NIH. You can ask about treatment there, or ask for recommendations for nearby clinics that may be a spin-off from them. Here is the number: 1-800-411-1222
NIH is a federal government agency, whose charge is biomedical & public health research. In general, it sponsors studies done in other venues, or collects and analyzes data from studies, journals and reports. NIH is not (as far as I know) doing primary patient care, but through your physician you may be a participant in one of their studies. I look to NIH as a source for scientifically vetted information. Perhaps the previous poster was referring to "NJH," short for National Jewish Health, which is a big & well-respected provider of care for lung ailments, does a lot of research on the issues, and hosts an annual(?) conference on Bronchiectasis and related infections.