(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.
@imeehaigt .. imee I is SO nice to hear from you again! Thank you for sharing! I SO totally agree with you on the exercise .. I find when I exercise I ALWAYS bring up extra sputum .. I try to use my Aerobika right after .. SO important!
When you say "expel sputum everyday as this is ground for bacteria" .. SO true! That sputum .. NOT expelled becomes a breeding ground for all kinds of nasty critters .. SO it is important for you to CONTINUE to get check ups with a good Infectious Diseases Doctor. So do keep us posted on your progress .. again .. so good to hear from you! Hugs! Katherine
@windwalker Hi Terri, it's quite scary to think that's where I got sick from...but it sure would make sense. I guess we all suffer from immunodeficiency & lung impairment to varying degrees which creates the perfect storm & we end up with MAC/Bronchiectasis.
Something of interest to me, was that I found some of my medical records from 2009 (2 years into my illness) & the diagnoses listed Bronchiectasis. Well it wasn't until this past Fall that they told me that I had Bronchiectasis. I'm not sure how I missed that...maybe they just didn't tell me or I was so sick that I just didn't matter to me!!!!
Anyways, I know it doesn't do anybody any good to try & figure it all out but rather focus on where we are right now. The epidemiologist (which I LOVE) in me loves to piece things together, to map out the journey of an illness. I'm not trying to dwell on the "how, when, where & why's" about it...it just interests me, that's all. And I'm glad to hear your input/feedback, so thanks, Terri!
Best,
Jen 🙂
Windwalker....really?? NTM might be contagious human to human?? there might be a silver lining to that...sorta.... it might become a "reportable"condition hence CDC would have to track folks.tdrell
Wiindwalker ....fascinating re the Alpha 1.anti trypsin carrier possibly having correlation to our favorite NTM.....4 Months after my appt at NJH, the NP who works with my DR ......I am a carrier....since my levels were low, they sent the specimen to a speciality place for further analysis. She did not mention any correlation to my situation ( i Am not on NTM RX ....they feel my issue is GERD/aspiration of water containing NTM) but felt my children need to be aware and be tested...along with partners and children.
Interestingly, the NP confirmed I would return for CAT and sputums after a year. Tdrell
yes windwalker and tdrell,veery interesting. Maybe I gave it to my sister in law. She is a nurse though so may have already had it.
Yes CDC involvement would be good for us, cure would have to be sought or we infect the human race!! Have to find out more about this, can you post video? Thanks xo
Do you have the link to the videos?
Jo Ann
That is wonderful news
JO Ann
Thanks...from the heart
Wow this could be catching? I have always thought that when I cough or sneeze that these little bugs could come out, how could they not. Makes sense to me. Thank goodness they are doing research on those nasty critters. thanks for the info @windwalker . I will watch the videos asap.
@jentaylor
Same here Jen. Not dwelling, just curious. By the way, I too was diagnosed with
bronchiecstasis years before I was told. It surfaced in records retrieved from a
long ago doctor's office. I was upset that I was never told about it. It was in
records going back to 2000, but it took my Mayo doctor getting those old records
in 2013 to tell me about it. Oh well.........can only take care of the here and
now.