(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.
Who do you see at the Mayo? And which one do you go to?
Thankyou so much for responding. I do have bronchiectasis as well :(...I started the 3 pills for 2 wks and got ill. I was told I have nodules on my lungs, is that what you mean by cavities? Which meds do you take now. I’m so scared and confused about stopping the 3 or doing another treatment. I worry about how fast will my lungs deteriorate? My pulmonologist said I have plenty of lungs left, I’m 52, and he was more against treating because it returns and is hard on the body but my infectiuos desease dr put me on biaxin, rifabutin and ethambutol at first visit but I had to stop I just got ill. I don’t cought. I do have mucus come up in the am, I am very tired when I get home from work and my breathing is heavy at times. Gosh will that get worse if I don’t do treatment? I also wonder what else can I do/take to be proactive? I’m sorry for all the questions, I just am worried about the future 🙁
Yes thankyou so much for responding. Wow, you are taking antibiotics for over 2 years? Hope you are doing well :)... I don’t want to continue with the 3. I want to be as proactive as I can so that I can have a good/decent quality of life but I am so overwhelmed at times and don’t know what to listen to 🙁
Do you have a fb group? I wish you would :)....Things like this are easier when you know you are not going through it alone.
@barbjh Good morning Barb. I see Dr. Leventhal at the Jacksonville, Fl. location. BTW, he has given me permission to quote him on what I post in these pages. Is your mac stable at the moment? -Terri
@bleo Hi Betty. How are you feeling?
@soflo I could give you better suggestions if I knew more about where you are with your disease. How sick are you at the moment? Do you have bronchiectasis?
@soflo, First and foremost, if you are not doing the nebulized saline treatments, you probably should be. It is straight up salty mist, not a medication. Research shows that this does help in making the mac recede. My dr has me on 7% sodium chloride (saline).
@windwalker ...bless your heart for all the work you do to help us cope and get better. I cannot tell you how uplifting your post was that said using a saline solution and nebulizer makes a very hostile environment for MAC. I feel as though i regained my sanity reading that! Looking forward to your FB page!!
Yayy Terri on the fb page