(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.
@auntnanny it's a subset of MAC; stands for Mycobacterium avium-intracellulare whereas MAC is Mycobacterium avium complex. And no surprise that you never heard of it...lots haven't!
@windwalker what made (makes) you case unusual?
Thank you and no, I've never heard of it. I have a lot to learn
@auntnanny
Hi Jan, MAI is another type of mycobacterium, it is Mycobacterium Avium Intercellular. That was my diagnosis in December 2016 after removal of a lung nodule. I had no symptoms except for the constant throat clearing and cough. Sometimes worse than others but usually not bad. I haven't been prescribed any antibiotics yet.
Gina K
Thank you, Gina...... I learn something new every day. Do you know why they haven't prescribed anything yet? Due to surgery? Just wondering.
I was diagnosed COPD with bronchiectasis for almost 6 years now after having coughed daily for all the previous years. Amoxicillin and Rulide failed to work on this flair up so am on ciprofloxacin, So much time and money is being spent here in NZ making sure that the doctors and nursing staff are treating patients but yet nothing is happening,if not for a herbal medicine i wont be able to get rid ofbthis disease,
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*Moderators Note*
As outlined by the Terms of Use https://connect.mayoclinic.org/terms-of-use/, no commercial postings, advertisements or solicitations are allowed on Mayo Clinic Connect. Mayo Clinic does not prevent members from discussing alternative medicines, second opinions, and treatments, however, this guarantee of a cure from an herbal center has no affiliation to Mayo Clinic and has not been approved by the FDA.
@auntnanny
Hi Jan, The doctor I'm going to at NYU, David Kamelhar, (got him from the American Lung Assoc, NTM* website), said since I have no symptoms and barely cough up anything at all, he would advise waiting on antibiotics. He prescribed using an Aerobika two or more times a day to try to cough up mucus from the bronchiectasis, but even with that I barely cough up anything. I just recently had a sputum induction, (again barely coughed up anything during that), but I don't see him until Oct 9 for results since they said at least 6-8 weeks to see if anything grows.
I've read on here quite a few people don't get treated immediately, depends on symptoms I guess. Don't feel concerned about asking any questions on here, there's always someone who has some information. I don't feel very knowledgeable about all this either since I've only started this journey a few months ago. I just try to find out as much as I can, watch whatever videos are posted from conferences, and read what everybody else has learned along the way. Some of it applies to me, some of it doesn't, but as Katherine and many others have said, "knowledge is power". So I try to learn as much as I can from trusted sources.
Hope that explains a little.
Gina
*NTM = Non Tuberculosis Mycobacterium
A cure would be absolutely miraculous...... when I was diagnosed after years and years of wrong diagnoses, -- Mayo's told me bronchiectasis is a chronic disease -- they cannot cure it but they can manage it. I asked my doctor there if I was going to die from it (because I had lost a lot of weight and was really ill)..... he smiled and said "You will die with it -- but hopefully not from it". I keep telling myself that. And.......... they have helped me manage it now for two years. I'm very thankful for them.
Thank you for explaining NTM -- I didn't know that either. I have no trouble coughing up when I'm having a flare -- which seems to be about once a month. So, I'm able to get a lot for the sputum testing.
The way it was explained to me by several doctors is that one should not wait to be treated regardless of the degree of symptoms because MAC/MAI will continue to do damage, so the sooner the better in terms of treatment. My doctor at Vanderbilt says that in time more and more physicians will say treatment is necessary for all who have been diagnosed.