(MAC/MAI) Mycobacterium Avium Complex Pulmonary Disease: Join us
I am new to Mayo online .. I was hoping to find others with .. MYCOBACTERIUM AVIUM COMPLEX PULMONARY DISEASE (MAC/MAI) and/or BRONCHIECTASIS. I found only 1 thread on mycobacterium accidently under the catagory "Lungs". I'm hoping by starting a subject matter directly related to MYCOBACTERIUM AVIUM COMPLEX PULMONARY DISEASE (MAC/MAI) I may find others out there!
I was diagnosed by a sputum culture August 2007 (but the culture result was accidentally misfiled until 2008!) with MYCOBACTERIUM AVIUM COMPLEX PULMONARY DISEASE (MAC/MAI) and BRONCHIECTASIS. I am now on 5 antibiotics. Working with Dr. Timothy Aksamit at Rochester Mayo Clinic .. he is a saint to have put up with me this long! I was terrified of the treatment . started the first antibiotic September 3, 2011 ... am now on all 5 antibiotics for 18 mos to 2 years. Am delighted at the very bearable side effects!
I wrote on the 1 thread I found: If you google NON-TUBERCULOUS MYCOBACTERIUM AVIUM COMPLEX PULMONARY DISEASE (MAC/MAI) you will learn a LOT about the disease. But PLEASE do NOT get scared about all the things you read .. that is what I did and nearly refused to do the treatment until after a 2nd Micomacterium was discovered! Educate yourself for "due diligence" .. but take it all with a grain of salt .. you are NOT necessarily going to have all the terrible side effects of the antibiotics! Good luck to you!
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January 2017 Update
One of our great Connect Members .. @Paula_MAC2007 .. had a wonderfully helpful idea that I wanted to share! Her idea .. as you read through the pages to gather information on our shared disease of MAC you can develop a personal "file cabinet" for future reference without the necessity of reading all the pages again!
If you have the "MS Word" program on your computer:
- Document Title Example: Mayo Clinic Connect MAI/MAC Information
- Then develop different categories that make sense to you such as: Heath Aids .. Videos .. Healthy Living .. Positive Thinking .. Baseline Testing and Regular Testing .. Antibiotics ..
Tips for
- As you read the pages .. copy/paste/save things of interest into that MS Word document under your preferred categories for future reference.
Then as you want to refer back to something in the future .. YEAH! You have now created your own personal "file cabinet" on MAC/MAI! Go to it!
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
I too had sputum inductions and no results. My ID MD did test on IGG, IGM and IGE antibodies. My IGG and Subclass I was slightly low. But so far no treatment
for either. I am starting on Zantac for Reflux
JO Ann K
What herbal remedy are you using
Jo Ann K
Hello! My case is unusual in that I have a genetic defect that Mayo does not understand. My lung lung function has been steadily dropping over the last 15 yrs without explanation and they don't know why. I am now at a scary 44% lung function. Was told that they have seen cases like mine suddenly plummet and will be in total lung failure. That is why I was pre-qualified last fall for a double lung transplant.
Did they test your Immune Function?
Jo Ann Kiemen
Becky, I had my sputem test done at Mayo Clinic in Florida 5 weeks ago. (for MAC and pseudomonas) As of last week, the results were not back yet. I will call again today. I know they send the Florida samples to the Mayo Clinic in Rochester's to test. I know MAC is a slow growing bacteria and it takes at least two weeks for it to grow; then I have to add in the shipping time of the samples. I am not sure how anybody can get a faster result over several days time. Will have to investigate.
Irene, I believe that to be very true. I have a feeling I had MAC awhile before it was properly diagnosed. I feel like that is why my lung function is down to 44% now. I think much of the lung tissue got severely scarred and damaged before it was caught. It is very confusing because many doctors, including my beloved one at Mayo, do not believe in treating MAC right off the bat. (unless it is severe) I would like to go to the next NTM Conference next year and see if there is any new info out there.
Not true! I have bronchiectasis /mycobacterium abscessus and I never had a lung problem and do not have a compromised immune system. My doctors say I am rare case at both Mayo and UH case medical center. I basically have no symptoms but have started the meds to hopefully stop it. 1 azithromycin, 2 iv cefoxitin, and 1iv amikacin.
Sounds like a plan!
@tutti Lisa, I don't have compromised immune system either. But, with bronchiectasis, both of us have compromised lungs. although I have not had any lung function problems either. Having bronchiectasis, which has no cure, means that we are susceptible to invasions of bacteria of various kind in our lungs. I'm not on any long term antibiotics and my conditions have not worsened since my initial diagnosis. For that reason, my pulmonary doctor and I have both agreed to put off drug treatment until/unless my conditions worsen. From reading everybody's posts on this forum, it is clear that people all have different physical conditions and our doctors don't necessarily agree with each other on how these diseases (brochiectasis, MAC, and other accompanying lung problems) should be dealt with. So it is very challenging for us as patients to make decisions on what is the best steps for improving/maintaining our own health, especially challenging because we all will have to live with bronchiectasis for the rest of our lives.
@windwalker Got it...and that's quite unfun...You can have one of mine but guessing you wouldn't want it...any news on date of transplant?