(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.
@rvan I also started meds with a low BMI, I was 47kgs, I started on Fortisip (made by Nutricia) ready made drinks they were yummy and helped put the weight on, a gastro specialist saw how skinny I was and prescribed them for me, a life saver. All the best Heather
Thanks Heathert - good info, and a good idea. I will give those a try. 🙂
@rits Love your mental imagery! I, too, have done the same thing in my head but not in the great detail that you have!! Go warriors!! Get through that biofilm! Nan
Hi Heather,
I don't know. Mycobacteria seem to be ubiquitous, so we all are exposed to them, but only some - very regrettably - are affected.
Yes @bolso1, me too -- I've seen some research in the past, and more recently, on enzymes and biofilms in the body and many other applications. But so far, no enzyme lung treatments yet for NTM biofilms.
(NB. Folks, some enzymes have been sold in shops or online for a while, but unfortunately, most are for the gut and digestion -- no use for the lungs. Sadly, they cannot help us with NTMs).
In recent years, there's been a little research on enzymes for biofilms in the lungs that's more promising -- e.g. for Pseudomonas Aeroginosa in people with Cystic Fibrosis etc. For example, getting an enzyme like pyruvate dehydrogenase (NOT pyruvate dehydrogenase kinase) with an antibiotic like Tobramycin -- so the biofilm from p.Aeroginosa is attacked as well as the bug. But there are some risks. And there's no inhalable drug yet -- or any research for an inhalable drug yet.
Unfortunately, nobody should 'hold their breath' waiting for a treatment of this kind. A lot of this research is very small-scale and unfunded, or given very little funding. It might not be taken up by drug companies for decades, if ever -- unless there's an ongoing, public push for it.
The so-called 'big 3' we're often given for NTMs are 3 antibiotics that have actually been around for 60 years! Good grief, 60 years!
Back in those days researchers didn't know much about biofilms, and many still don't These drugs have also been inherited from other illnesses -- e.g. Tuberculosis, or Leprosy.
Additionally, some of our doctors and pulmonologists either aren't 'awake' to the fact that drug companies really only test new drugs on free-floating planktonic bacteria, but not on the bacterial biofilms as well (because they'd need dangerously high doses to get through biofilms); or they're just pragmatic -- they're only going to treat NTMs with what's already available. Period.
But one thing Covid19 has taught us: it's really just a matter of 'will' how quickly research gets done -- and a matter of increased funding for medical research and medical applications.
@rits Hi Rita -- hey I'm with you! I hope the Arikayce helps me too.
Yes Arikayce and Azithromycin have been shown to get into the outer layers of NTM biofilms, in certain circumstances -- but quite often they can't get all the way into the biofilms as well. Even Rifampin can sometimes 'shrink' the biofilm a bit too. But these NTM drugs are not really anti-biofilm drugs -- and they were not designed to be.
In the recent past, research on liposomal -- and even smaller nano-particle -- drugs has been showing more promise than the old drugs for NTMs. It's likely that some of these new drugs will have a better chance of getting further into biofilms because they're so small and inhaled into the lung, but these aren't actually anti-biofilm drugs either.
Also, any potential new drugs could be years off yet. (Good things are meant to come to those who wait -- but maybe we should shout louder, not just patiently wait!)
That said, I hope the inhaled Arikayce helps me and you both -- and soon.
Good luck to all of us!
Annie
Yes Sue @sueinmn, me too -- I really hope this research will accelerate.
(Maybe we should join with other groups where bacterial biofilms in the lungs are a real problem for treatment, like people with CF or COPD etc, to make our voices louder ??)
Annie
Annie - I think joining forces is a great idea - unfortunately, this is not something I can put on my radar right now - there is much on my plate. I would support anyone here who starts the effort.
Sue
Yes that would be a good way to get heard more readily. And the best way to do so is with a petition to the CDC...With the help of Mayo, reaching out to its vast list of folks with all three diseases...which starts with the staff person overseeing these forums.
@boomerexpert, lovely to see your smiling face again, hope all is going well! Take care Heather