(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.
@nick52 @liangctoo a good therapist will do that...
@liangctoo , I can't remember if you told us your mom is already seeing a therapist or not. But I agree with @boomerexpert . If she already sees a therapist, you should ask her to look into whether her meds for depression could cause some of her physical symptoms. But if she is not on any meds for depression, then her symptoms could very well be caused by her depression. She should be treated for this mental illness right away.
General question: how often did you get a CT Scan for MAC and/or bronchiectasis? Every 6 months, once a year, or ?
I would be curious too!
Moving to North Tampa. Does anyone know of a good MAC doctor?
@joan912 , Hello Joan. My doctor at the Mayo Clinic said he doesn't like a patient to have a CT Scan more than once a year, unless neccessary. CT scans are very powerful and can cause changes to your cells and DNA, so it is wise to only do get one infrequently. There is info on the precautions of scans on Google. Just be sure to go to ligit sites like Mayo, Johns Hopkins, etc. so that you get the real scoop.
Thank you, Terri. I think that's prudent. I believe certainly no more than once every 6 months, and preferably once/year.
@joan912 My pulmonary doctor does not like to order CT scan frequently either. I had one done when I first diagnosed. The second one was ordered last week after 3 years of the initial diagnosis. He does, however, order a chest X-Ray to be done every time before I go to see him (which is every 6-12 months) so he can make the comparison.
@suenfl Hello Sue. There is a good medical school in Gainsville at University of Florida. I have read many positive things about them. That location is a bit north of you. Dr. Fennelly is there, and is very knowledgeable with treating MAC patients. Of course, even further north in Jacksonville is our renown Mayo Clinic; that is where I go, and find that it is worth the drive. My doctor is Dr. Leventhal, (I adore that man!) I would be interested in knowing where you end up going. Good luck with your move, -Terri.
@suenfl although Terri is correct re: Gainesville & Jacksonville, I'm aware of the hours-long drive they entail. That said, there's a dearth of good doctors of any sort in the Tampa Bay area...this is where the mediocre ones go to pretend to work...try docs associated with Tampa General/USF Med school...