(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.
Dear Cowboy,
Glad you found a source. Hope you get relief. They tested my cough with medication for two months to see if I had acid reflux, but alas i did not so that's not my issue. Best wishes,
David
Dear Lisa, Sorry to hear of hoarse voice. Must be frustrating. If it is post-nasal, have you checked your allergies. Or maybe a sinus specialist. They are doing new stuff now days.
I don't think there is a lot of radiation in CT scan. They are quick and localized. You might research how large a dose of radiation one CT gives compared to something like the cancer radiation some people get.
Blessings
David
Hi Katherine,
I saw your latest coughing reply. When I am in a bout of coughing, I find that chewing gum helps it calm down (or maybe it just calms me down! lol) Milk seems to aggravate it. Water doesn't help. Ice cream with a sweet topping can seem to start a coughing jag. I'm thinking maybe it's the cold sugary sensation. Anyway, different strokes for different folks!
Blessings,
David
Hello Lisa, I can see where you coming from. I too have pressure on my chest, having hard time breathing sometimes and aching on my back. My pul. Dr. said its my acid reflux but I think is from my lungs. A friend of mind said who had NTM said is 1 of the side effect of the medicine. I have been on the 3 meds for 4 months now and Nov. I will see my Dr. and said I will have CT scan. I really can't tell if the meds are working. The only relief I get when I feel the pressure on chest and back is prayer and rest. I can't do all the things I used to do without stoping and rest. I will have you in my prayer and look at the bright side. Cila
Dear Readers,
Many thanks to the contributer who suggested the videos on lung disease from the national jewish health conference! It is at:
https://www.nationaljewish.org/ntmvideos2016
They were very clear and helpful and informative!
Hats off to you!
David
If the test they did for reflux was to put you on a PPI drug, they don't necessarily help airway reflux ( the kind you get symptoms from like post nasal drip, coughing but no hearburn). Mayo does a 24 hour Impedence test which is the only test that is definitive I was told, for silent reflux. Silent Reflux can cause MAC in some casas so I'm having the test, hoping to get rid of my MAC but making sure Reflux does not cause it to come back.
This is just what I was told. Others can weigh in on this.
Thanks
Kay S
Where in the New York area? You man Manhattan/the Boroughs?
David1952....since you benefited from National Jewish 2016 NTM workshop videos....you might also like the ones from 2015....go to same web site bit dont fill in any date at the end.tdrell
Lisa2860 I believe NationalJewish in Denver has a sattelite at Mt Sinai in Manhattan.tdrell
Hello Lisa, I really agree with Kay .. I have had the CT scans and feel if it helps my doctor take better care of me .. make a better diagnosis of my progress .. then I will definitely do it! It might help you feel better if you see the below website.
This website explains it really well:
http://www.radiologyinfo.org/en/info.cfm?pg=safety-xray
Essentially a Ct scan is: 10 mSv and Naturally-occurring "background" radiation exposure : We are exposed to radiation from natural sources all the time. According to recent estimates, the average person in the U.S. receives an effective dose of about 3 mSv per year from naturally occurring radioactive materials and cosmic radiation from outer space. These natural "background" doses vary throughout the country.
Also, Mayo Clinic gave me a nasal spray that has really helped me with the post nasal drip. I didn't think I had it either .. but my doctor took a look at my throat .. said yes you do .. and I had to trust him! A bit of a hassle in that I have to get the nasal spray from Mayo pharmacy .. and it has to be refrigerated .. BUT it works so I do it!
I wonder .. kind of sounds like you do not have a lot of confidence in your current doctor? Personally I think that is SO important in the over all recovery of our disease. Wonder if you really do want to seek a second opinion? Elsewhere on our Forum I have detailed how I have gone about finding a new specialist for myself or my husband. If you are interested in doing that .. you might read back posts?
Hope the above helps just a little bit! Sending you a hug! Katherine