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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Very well stated!
Thanks!
I’ve heard this before @alleycatkate but I’m really struggling trying to find a way to lessen the pain in my foot (pretty much a constant 5). I certainly do NOT want to complicate my lung issues AT ALL! I’m doing physical therapy for my foot and my ability to walk improves, but the pain level will not abate yet. I guess I better not take any chances but find other ways to lessen foot pain through some other means........I am going to the bronchiectasis workshop in Denver next weekend and I am excited to learn as much as I can about this illness.
I still can’t get my email to do what you are saying here. The only way that is seemingly working is to go to the group site and click on the bell, which brings up all the messages. I’m not the best at technology, but it used to work swimmingly....
Tell me more about this bronchiectasis workshop in Denver. How did you find out about it?
@frananthony I read about last year’s workshop on this site somewhere. It is sponsored by National Jewish Health and I have a website listed on my confirmation, if you’re interested in looking at it. http://www.njhealth.org/CME
Thanks!
Hi @migizii I'm sorry you are continuing to have problems with your email notifications. Please go to the following link to fill out the "Contact Community Moderator Form" so that we can try to take a closer look at the problems you are having.
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@nick52 Hi Nicole!! I can’t believe I am just seeing your message from 2018!!??? I think I entered the twilight zone….and never found my way out!! Haha. Somehow the settings changed on the Mayo site at one time but not sure that I can blame this oversight on that!! I hope you are doing well and maybe have kicked this disease to the curb. Be well.
Hugs,
Kate
@alleycatkate
Hi Kate,
I have been out of this site for a long. I am so glad to hear from you! Glad you made it through with that Covid Virus. I am glad I didn’t catch it but my husband did! I am feeling very well so I can thank God every day for being so good with me. Hope we can see you in Florida. We will be leaving the last week of November or first week of December ti go back to Palm Hill in Largo. Take good care of yourself Kate ! Love and hugs!!!
Hi,
It is normal if the Mac is active. My specialist thought it was better for me not getting on antibiotics because I didn’t have much symptoms. When I feel congested , fatigue andbreath is different. I take Clear lungs. Or my surgeon do a bronchoscopy to wash my lungs once a year or every two years. I am on my third year right now. It wii probably be worst with the antibiotics. My specialist said he recommends it when the patient has a lot of symptoms, Good luck with it! I never regretted my decision to use less invasive treatment. I am doing really good!