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.
@pfist Good morning. I am glad your mac receded on it's own. You are lucky with that. Mine just made me sick and cough non-stop for years. I had to go on some antibiotics at least. I am thrilled that you are doing the saline. We ALL need to be doing that.
It is odd how some MD's tell you to hold off until you really need to on the BIG 3 and other's tell you to go on it. I am still waiting and waiting for the Nitric Oxide study results of a small study and the FDA to allow the company AIT Therapeutics to start their Inhaled Nitric Oxide treatment. Some people have also done Inhaled Amikacin and I have also heard of trying other antibiotics
I also love how they scare us with the severity of the disease but in general, I feel this county and our CDC and FDA and pharma companies do not take this seriously and we are left to flounder.
@rmason I remember you had said that in a previous e-mail to me, so I asked my dr if his. MAC treatment plan was published. That is when he said he isn't treating my mac , rather is treating my bronchiectasis. He said he has thought about publishing his outcomes. He then followed up with "his proof that his treatment plans work is by the successes like me." He also stated that the way he treats mac is a recipe they tend to follow there at Mayo. I told him that wasn't entirely true, that I have Connect members that go to Mayo and get put on the Big 3. The expression on his face was that of disappointment. He then said "I know, there are a couple of drs there still sticking to the old school way of treating it (at the Rochester Mayo). Pretty much, no drs at the Mayo in Florida would use the Big 3 to treat mac unless it was a severe and cavitary case. You are in charge of your own health and treatment. YOU can ask to try a different treatment plan and tell them you want to try specific drugs. State specifically what drugs you want to try. Most will work with you. Let me ask you this, does your dr have published success stories on using the Big 3?
@jkiemen There is inhaled cipro too now, but I just use the pills.
@jkiemen It is not only this country, the ambiguity is worldwide. Mac is truly a tough nut to crack.
@jkiemen, you are right about the scare tactic. My doctor said mac is so slow growing, that it would take 50 yrs to follow a patient with a placebo group/treatment goup. That is another reason it is hard to get proven treatment documented. Because it is slow growing, you all have some time on your side to try another course of treatment. That applies only to avium bacterium.
@rmason Will you ask your physician for documented cases of conversion? Conversion is when a person is totally free of mac and it never comes back. I would be very interested in seeing links stating such.
Thank you for this information.
@jkiemen Have you contacted the NO group recently to see where it is at as far as a release date?