(MAC/MAI) Mycobacterium Avium Complex Pulmonary Disease: Join us

Posted by Katherine, Alumni Mentor @katemn, Nov 21, 2011

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.

Terri Martin, Volunteer Mentor | @windwalker | Jul 21, 2017

In reply to @kathyg "Hello, Kate What a coincidence that my first name is Katherine/Kathy. I was just diagnosed with..." + (show)

I was treated the same Cindy, on my first MAC infection back in 2005. It stayed dormant until 2013, then I was treated by alternating months of Cipro for 10 days one month and then the following month 10 days on Doxycycline. That cycle went on for another three yrs as a preventative measure to keep the MAC from colonizing. I did get 'pseudomonas' last Spring. It is another lovely bacteria that likes to attack weakened lungs. I did ask my Dr why he chose not to treat me with the BIG THREE antibiotics; he said he does not believe in it as a first line of defense. He saves that for chronic cases (repeat offenders) and the seriously infected. Doctors have different theories on how to treat MAC. It is only in recent times that this disease got much attention. Plus, the treatment is not a one size fits all kind of thing.

Terri Martin, Volunteer Mentor | @windwalker | Jul 21, 2017

In reply to @colapyrus "Does anyone have the list of tests a person should be getting routinely if they are..." + (show)

Hi Linda. Was wondering where you store and pull out these posts that you save? And then, how do you repost them? If it is too complicated of an answer, I will ask Colleen. I have saved some by bookmarking it to my profile page. Is that all I need to do? Thanks!

Terri Martin, Volunteer Mentor | @windwalker | Jul 21, 2017

In reply to @cila "Hi Catherine, when you inhale amikacin did you do coughing while your inhaling it? Also my..." + (show)

Hi Heather! Yes, please do keep us posted about your results.

lindam272 | @lindam272 | Jul 21, 2017

Terri, I took a few hours one day and went through the emails that I had not deleted and stored them in folders in my email system. One group I created is "Testing - standard of care" which is where this email was. I copied it and pasted it in the reply post to Jan. I am happy to help whenever I can! Linda

tdrell | @tdrell | Jul 21, 2017

In reply to @kathyg "Hello, Kate What a coincidence that my first name is Katherine/Kathy. I was just diagnosed with..." + (show)

Windwalker.....thanks!!! Tdrell

Jo Ann K | @jkiemen | Jul 21, 2017

In reply to @kathyg "Hello, Kate What a coincidence that my first name is Katherine/Kathy. I was just diagnosed with..." + (show)

He said that the Mycobacterium Intracellulare type is generally from Soil

heathert | @heathert | Jul 21, 2017

In reply to @kathyg "Hello, Kate What a coincidence that my first name is Katherine/Kathy. I was just diagnosed with..." + (show)

yes but water comes in contact with soil at some stage i guess.

ginak | @ginak | Jul 21, 2017

In reply to @kathyg "Hello, Kate What a coincidence that my first name is Katherine/Kathy. I was just diagnosed with..." + (show)

@windwalker Hi Terri, I also see that pink looking film in the corners of the tub/shower if I don't clean for a few days. I saw it at my home in Brooklyn, NY where I lived for 23 years and I see it here, at my new home in Staten Island, NY, where I'm living since Feb 2017. I was diagnosed in Dec 2016 so I guess I got it while living in Brooklyn. I remember reading something about if you have the pink bacteria you don't have the MAI/MAC bacteria in the water. Do I remember this correctly? Or have I misunderstood that?
P.S. thanks for becoming our volunteer mentor, it's really appreciated. Also, I hope all goes well for Katherine and her husband and she'll be able to "pop in" now and then to say hello.
Gina K

Colleen Young, Connect Director | @colleenyoung | Jul 21, 2017

Hi @cindymc and everyone,
I find it useful and helpful to reply to message on the Connect website, rather than reply by email. This allows you to see not only the single message that you're responding to, but the whole conversation, including other replies that other members have made. It becomes more of a conversation around a table rather than one-on-one.
Here's how to get to the discussion on the website from an email notification.

How to reply on Connect
1. Open the email notification
2. Click the VIEW & REPLY button at the bottom of the email.
This will take you directly to the message in the discussion thread. You can then scroll through the messages before and after.
3. Click REPLY and type your response.

Not logged in?
If you're not logged in, then you will have to login first to reply. If you're using a private computer, tablet or phone, you can choose to stay logged in. This means that you won't have to login every time you go to the site. (If you use a shared or public computer, I do not recommend staying logged in.)

How to Login
1. Click LOGIN in the top right corner. (On mobile, click Login in the menu.)
2. Enter your email and password.
3. Check the box that says "Keep me signed in."
4. Click Login.

Don't hesitate to private message me if you have additional questions.

tdrell | @tdrell | Jul 21, 2017

In reply to @kathyg "Hello, Kate What a coincidence that my first name is Katherine/Kathy. I was just diagnosed with..." + (show)

Ginak.....i think I heard Dr JOseph Falkingham say itbin the 2016 National Jewish video presentation he gave. I recall the name he gave these NTM fighters as called METHO....something.tdrell

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