(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 also live in SouthEastern Wisconsin
Jo Ann Kiemen
@jkiemen Hooray! Looks like we have a few Wisconsinites on this forum. Go Badgers! Go Packers! Not that I'm a sports fanatic. But I'm very loyal to my state. 🙂
I lived in Milwaukee for 24 years before I moved south. Love me some Packers!
Hi im sophie and live in milwaukee with MAC. Do you have mac and when were you diagnosed....
Bonniewhite56, sophie1019,jkiemen, ling123, and if i recall a member named Paula has a Wisconsin connection!
Tdrell
I have noticed this pink orange film since I moved and have well water
Who do we inform?
JO Ann
Sofia, About a year ago my health problems began.
I moved to Savannah 3 years ago. My history is that I've had pneumonia practically every year for 6-7 years. First year here I had it again. I developed a very bad cough that would not go away a year ago, doctor referred me to Pulmonary doctor and he began to run test upon test upon test.
I am going to mayo for second opinion next month.
I miss Milwaukee but not the weather. Not sure the humidity here is healthy for me though.
Bonnie, I had the same scenario with the repeated pneumonias. Only, I think now, that I may have have some kind of mycobacterium infections that went undiagnosed. None of the doctors ever did a sputem culture when I had 'pneumonia'. It finally dawned on me that something wasn't right because it just wasn't normal to be sick like that so often.
I live 21 miles north of you in Bluffton near Hilton Head. We should do lunch some time. This is the most comfortable climate that I have ever lived in. I am close enough to the beach that the soil is very sandy, therefore, rainwater drains away quickly and it never feels terribly damp to me. The winters are cool, but dry. I grew up in Virginia. The weather there was killing me!
Hi Jo Ann, most well water is free of MAC, hopefully your's is. If you could tell me what region you live in, (state & county) I will relay it to the researcher along with mine. His name is Joseph Faulkinham, III. He is at Virginia Tech. He has interesting clips from the 2017 Conference on YouTube. They are lengthy, but interesting. That is where I saw him say that he would be interested in knowing where this pinkish orange bacteria can be found. Thanks! Terri M.
Hi Sophie! Welcome to our forum! My experience was that I became extremely ill with MAC in March of 2007. I was told I had bronchitis, was treated for that, did not get better, then I was told I had pneumonia, was treated for that, still did not get better. Finally was diagnosed in August! It took five months for someone to finally give me a sputem test to see what I actually had! Then they did a bronchoscopy to make sure. I knew I had something God aweful back in March because I had pneumonia many times in my life along with other lung infections. None of those felt quite like this one. This one felt different, I knew it was something bad.