(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.
@unicorn .. Christa this is JUST me .. but if a member is deciding between purchasing an Acapella OR an Aerobika .. I would vote for the Aerobika EVERY time .. it is SOOO effective at getting up the mucus .. so much more than the Acapella. I have put on our Forum a resource for about $60 that I have had good luck with twice. This is just my opinion and experience. Hugs to all! Katherine
I agree with Katherine. I drink a lot of water all day long but still have sticky phlegm. We do need to drink plenty of water but sticky phlegm is the name of the game for sure. I've had it for over 20 years. Drive me crazy but manage to live with it.
@unicorn .. Christa good advice from your doctor! But personally I would recommend the Aerobika over the Acapella for being more effective at getting the sticky mucous UP and out of the lungs .. just my personal experience and opinion. I put info on getting the Aerobika for about $60 on our Forum. Hugs! Katherine
@windwalker Terri, neither my husband or I care for much garlic, nor do our closest friends. My husband is of Italian heritage and his parents didn't use garlic either! People have this impression that Italians eat a lot of garlic but when we have been in Italy none of the restaurants smelled heavily of garlic like many Italian restaurants do here. There are some we have walked into here and walked right back out of because the smell immediately assaulted us. I do actually like some garlic, I mainly do not like that for about three days after eating I feel like it's coming out of my pores.
JK
Thanks @windwalker i usually dont chew it i just pinch it and leave it for about 10 to 15 minutes and swallow it like capsule. I usally take it as soon as I wake up in the morning. Its been a year that i did not take antibiotics and whenever I feel like having sore throught I take it 2x a day.
I agree the smell is horrible thats why i dont chew it and make sure to brush and gargle with mouthwash. Also im worried too that my sweat will smell like garlic lol. Im just thinking of the benefits that I get whenever I take it.
totally agree, my acapella does nothing
@imeehaight Definitely the sweat and in the shower stall I can't stand the smell of myself.
JK
Looks like it got lost from the original post to which I replied...! I was referring to testing for Alpha-1 deficiencency
@boomerexpert, I am NOT an expert .. NOR a doctor but when I noticed on my genetic testing on 23andMe (a website that tests I think 1% of my genetic code) showed: "Detected mutation" is: PI*Z .. the most severe mutation .. increased risk for COPD. I then showed this report to Dr. Timothy Aksamit who showed a great interest in this genetic mutation and requested a copy of the report. Then in 2017 I met with Mayo Clinic Dr. Dulohery who notes in her bio: Interests Chronic obstructive pulmonary disease, Bronchiectasis, Alpha-1 antitrypsin deficiency, Asthma, Nontuberculous mycobacterial pulmonary disease.
I found it very interesting that an area of interest for her was: Alpha-1 antitrypsin deficiency. In correspondence she said: " If your testing indicated the Z mutation, we should complete full alpha-1 antitrypsin deficiency testing to determine which genes you have and if the level is low. I have added to blood work to your evaluation in July."
So @boomerexpert NOT being an expert I can only tell you .. a Mayo Clinic Doctor appears to be VERY interested in giving me FURTHER testing since my 23andMe testing DOES indicate the Z mutation. What all this means I do not have a clue since I am not a doctor nor an expert. I DO hope to gain further knowledge from Dr. Dulohery in coming months as it relates to my MAC and Bronchiectasis which I will share with our Connect Community. Katherine