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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@rmason Just wanted to add that Mayo physicians are highly respected around the world because they are among the best. Most other physicians do want to hear about what Mayo's cutting edge physicians are saying. That has been my experience anyway.
@windwalker ...agree re Mayo Doctors and how they are respected around the world. Unless it has changed, the doctors are salaried....not paid by the numbers of clients they see. They also have a medical school in Rochester Mn. This increases the quality of the care. The doctors are always “observed” by future Doctors hence 100% accountability.
Something came up last night at our amateur investment club monthly meeting. A Wisconsin ( where we live) based company Exact Sciences (Symbol EXAS) is a stock we bought and follow. It created Cologuard , a way to check feces for cancer without have to have a colonoscopy. Medicare covers it and it was recommended by GI doctors for select candidates.
All of a sudden the stock price zipped up 25% from the price we paid. We wondered why. I checked news for the company. It was stated that they created a new blood test with Mayo to check for a form of liver cancer. My conclusion: even to the financial world, Mayo Clinic is greatly respected. So if Mayo Clinic is involved, the product must be promising. Tdrell
@tdrell, Terri, those are VERY interesting tidbits of info. Thank you for backing me on the reputation of Mayo. I am headed to the Mayo in Rochester tomorrow for 4 days. Will get a tour of Mayo, and lots of learning. Will meet other mentors, and Colleen!
It would be interesting to know if they will be participating in any upcoming research on this
@jkiemen Hi Jo Ann. Reminder: need to put (@ someone'sname) at the start of your texted reply, that way it is connected to the conversation and person you are replying to. As it stands; I do not know what upcoming research ypu are thinking of. Thanks!
Thank you for the valuable information, and I'm so glad there is continued improvement for you.....I don't nebulize saline, but I'm going to start it, because what your Dr. Is saying makes sense...
Good point-I will ask him. I understand The National Jewish Hospital in Denver specializes in MAC. Would be curious to hear from members who have been treated there with MAC and bronchiectasis?
@windwalker I had gotten away from the nebulized saline treatments (in conjunction with a vibrating vest) but am getting back to that routine!
@windwalker...terri... that is exciting the trip to Mayo at Rochester MN. If time permits, check out in the “basement” of main Clinic, the glass sculpture of Dale Chiluhily..sp...hanging on ceiling.
Also in Reference Library ,if open see if there are articles etc on our enemies the NTM!!! Enjoy ! You have earned this trip many times over......don’t get overtired.
Terri aka tdrell
@cld120 So glad to hear that! There was a study in France before the inhaled saline was passed for use here. Their studies showed that saline alone got rid of mac. I will have to look for a link about that. I read about it 10 years ago.