(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.
Please add your doctor recommendations to this discussion so that others can find your recommendations easily. cc @unicorn
Good MAC Doctor? http://mayocl.in/2paMbB7
@ling123 Ni
how ma Ling. Two things you said about yourself sent up a red flag for me; that
is that you cough up blood sometimes (that is not normal & can indicate a
small localized infection), and that you cough up lots of thick phlegm. I know
you are putting off antibiotic use for as long as possible, but I feel like you
should at least be on the nebulized saline treatment. It will loosen and thin
the mucous so that it comes up easier. Since I have been doing it for almost a
yr now, my rails and wheezing have gone away. And my lungs are cystal clear.
Some of the credit goes to the tobramycin that I also nebulize for pseudomonas.
It is just saline, salt water, it will not hurt you. But it can do you a world
of good.
@ling123 This
is just me, I would not wait until Sept to discuss getting a prescription for
the sodium Chloride 7% inhalable solution (saline). It really is not a big deal.
He can send the scrip for it straight to your pharmacy. If you do not own a
nebulizer, have him write a script for that too so insurance will cover it. Can
be purchased over the counter as well. Sept is two months away. That is two
months of gunk gathering in your lungs that MAC and pseudomonas, or any other
specie of mycobacterium can take up residence.
@katemn What
Linda said is true about the Mayo doing x-rays mostly, and CT scan sparingly. My
doctor explained that CT scans are extremely strong and put out a ton of
radiation. Radiation is cumulative, meaning it adds up and stays in your body.
Too much radiation damages DNA and can cause cancer. I was reading an article
last night that was in the Washington Post about that too. In fact, someone on
this forum had posted the link, probably Linda, not sure. A doctor in that
article said that 'No medical treatment is all the way 'good' for you. All will
have some degree of damage. They decide when they treat if the slight damage is
better than not treating a disease."
@ling123 Ling and @windwalker .. Ling I just have agree with Terri .. I was on 3% and didn't feel it was helping enough .. I contacted my doctor and requested 7% .. it was so simple .. prescription was faxed to my pharmacy and boom it was taken care of! If you need nebulizer and compressor info just let me know. Just know that both Terri and I have down this road before .. AND gotten nasty critters in our lungs as a result .. if we didn't care about you we wouldn't be bothering! Hugs to you!
@katemn &
@ling123 True story Ling, we DO care! -
Terri
@windwalker Terri, very good reminder and information .. thank you! Hugs! Katherine
@katemn
Thank you for that info Katherine. Boy! I would just love to be in the lab
and see all of that stuff! I have always been intrigued with microscopic
things in general.
Thanks @katemn, i do have bronchaectasis and the blood is just a stain in mucus that was last sunday only. Ive been deligently doing my regular check ups and lab test my lab test result last jan was negative of NTM. As of now im not taking any meds except for my multi vitamins I continued to produce sticky phlegm and I noticed that it stopped when I started to exercise everyday. My doctor is very far from here so he prescribed me a reserve antibiotics in case I cough up blood. As of now I feel like there are lots of phlegm in my lungs but Im afraid to cough it out since I might cough blood. But im doing Ok still going to work everynight.
Hugs and kisses to everyone
@windwalker Thank you very much for your concern. I have been coughing up thick mucus for over 20 years. It is very annoying. But it has not prevented me from living a normal, active life. I don't have problems with breathing. No wheezing, either. I've in my 60's but still able to play tennis 2-3 times a week all year round. That's how active and healthy I am. I believe the mucus is caused by brochiectasis, which is the cause for me catching MAC eventually. But other than coughing up blood twice (first time pretty heavy, second time very light) in the past 2.5 years, I continue to feel fine. No other health problems with my lungs or other organs. But I do agree with you that I should look into how to improve my mucus situation. I will definitely look into getting the Aerobika that Katherine has recommended. I will also ask my doctor about the possibility of getting help with mucus thinning when I go to my appointment with him in September.