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!
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
@tdtell Thanks Terri. I love Chihuly! I am very excited about the trip, if I ever get there!! I was supposed to be there by 3 today. Flight got delayed 2 hrs due to severe thunderstorms in Chicago. Then no available flights to Rochester. (They were all booked) So, will try it again tomorrow....
@windwalker ...terri...what a terrible disapointment.
I will think of you tomorrow and send the white light that you make it!!! Terri ...tdrell
Thanks,Justin.
@tdrell Thank you Terri!
@JustinMcClanahan Thank you for posting this link, Justin. This is good to know. I will tag another member I think may have looked into this as well. @nick52.
@windwalker -Terri-I have been thinking about your doctors statement about “treating” your bronchiectasis not MAC-since bronchiectasis doesn’t get better do you think he means he’s preventing it from worsening?
PS-hope you have a good trip to Mayo in MN!
Roxanne
May I ask which meds do you take. I have Mac and experience everything you just mentioned. I started 3 antbiotics for 2 weeks but stopped. Thank-you 🙂
@soflo When you respond to these posts, please use the @name at the begimning like you see here that I did. That way it will connect the conversation to the post you are replying to and also the person you are directing it to. Thank you.
Terri, are you in Minnesota? If so, anywhere near the TC? I don't know of anyone else with MAC, and it would be nice to meet.
@windwalker Hi Terri, I was responding all over the place earlier sorry about that but now I think I got it lol... responding to your questions I live in South Florida, I do have both mac/bronc and right now I have difficulty breathing at times, I don’t have a cough but I do cough up mucus in the morning, fatigue, brain fog, pains in my rib cage, and over the years most of the symptoms were blamed on menopause. Thank goodness for my cardiologist saw something on my lungs which started this journey. A CT of my lungs shows nodules. So I started the 3 antibiotic treatment for two weeks but as I said I don’t know that my body can handle
It. My doctor will understand when I tell him I should get a nebulizer saline flush? So Terri I am very nervous as to which path to take because I just don’t know. I want to be proactive and I’d like to know naturally what else I can do to keep my lungs healthy from deteriorating even more. This site is amazing and I am so happy to have stumbled upon you all 🙂