(MAC/MAI) Mycobacterium Avium Complex Pulmonary Disease: Join us

Posted by Katherine, Alumni Mentor @katemn, Nov 21, 2011

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.

@nnassiri

Dear Katherine, and all.
My wife had been diagnosed few days ago with MAC. She had Bronchiaticsis since 2000. I really would appreciate it listening to you more about the medications you did, side effects, and how successful they were. I hope we are able to reach Dr. Timothy Aksamit at Rochester Mayo Clinic.
God bless you
N.

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Hi guys. Many posts about making home made ice cubes versus using the ice maker in the freezer. I do that also but I go one step further. We purchased a Berkey water filter about 4 years ago. It has a carbon filter and filters out more bad stuff than any other filter on the market. It's portable and doesn't require any installation. We take it with us when we camp and/or travel. (We are snowbirds). The unit we have costs about $300 but the filters last about 6 years depending on how much water you use. (Spendy investment but not if you calculate how much you will spend on filters over that time period). I have metastatic breast cancer and as a result my immune system is compromised so I feel really good about using this for all drinking and cooking water. (We use a personal water well for 6 months a year). We get no personal enrichment in promoting the Berkey other than making others aware of this wonderful product. Look up their website on the internet to get more details.

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@david1952

Dear Katherine and all,
I have a question. I saw on the Jewish Conference videos that there are 10 MAC species and that we should know which "bug" we have. But when i mentioned that to my Pulmonologist this week, she said there is just one MAC species. Which is correct?
David1952

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Thank you so much!

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@nnassiri

Dear Katherine, and all.
My wife had been diagnosed few days ago with MAC. She had Bronchiaticsis since 2000. I really would appreciate it listening to you more about the medications you did, side effects, and how successful they were. I hope we are able to reach Dr. Timothy Aksamit at Rochester Mayo Clinic.
God bless you
N.

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Wandering, thank you for your thoughts .. but our Forum is VERY concerned about Mycobacterium. Upon a bit of research I discovered one reviewer who said:

Big Berkey must be used everyday or bacteria will grow in dry filters, If you go on vacation have some one baby sit your Berkey, take it with you, dry out filters for 3.5 weeks turning everyday or just buy new filters for $107. Berkey needs to inform customers about this. I had to call Berkey to find out this information.

Frankly, even this one opinion was enough to concern me .. but then it appeared that the a big selling point for this product was removal of fluoride. On this Forum .. our concern is not taste .. it is concern of possible removal of mycobacterium.

So thank you for thinking of us .. but I am concerned that anyone on our Forum consider this product without REALLY researching it .. possibly reading reviews on Amazon.com? Best to you on your travels! Katherine

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@nnassiri

Dear Katherine, and all.
My wife had been diagnosed few days ago with MAC. She had Bronchiaticsis since 2000. I really would appreciate it listening to you more about the medications you did, side effects, and how successful they were. I hope we are able to reach Dr. Timothy Aksamit at Rochester Mayo Clinic.
God bless you
N.

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Yes I believe that is the unit that we have. After the water is filtered the bottom holds about 1-1.5 gallons. We don't use ANY plastic containers for our filtered drinking water. It takes some shopping around to find glass water bottles but that is what we use. If the filtering flow gets slow, they have instructions on how to clean the filters - not replace them. We have had ours for about 4 years and have only cleaned the filters a couple times. Quality product and the current price has actually come down since last year when friends bought one.

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@kwilbur

I haven't been contributing as much to this forum as I am in limbo about my lung condition. I spent half a day in the hospital expecting to have a biopsy of a nodule 9 mm - only to be sent home because the radiologist was afraid of hitting the wall of my lung and my having a collapsed lung. While at the hospital, I had another cscan done and the nodule had gotten small 7 mm , the size it was in June.

Oddly enough, I have stopped coughing up phlegm too - or very little. I was getting sick alot at the beginning of the school year which was treated with antiobiotics. Then I had the flu shot and I really don't know what is going on other than I do know I have bronchiecticus which is a constant.

I am able to keep up with a long school day, but don't do any work once I am home - about 6 p.m. Today I pressure washed my house - well with a light weight Home Depot system and a hose - and was able to keep up a strong pace for six hours. I only pray I stay on this path.

I know I have to remain vigilant but spending every day worrying is a waste of quality life. I was already in a mindset that I had lung cancer which now I truly doubt. It's not worth worrying about possible outcomes until they are a fact. I wish you all good health and stamina as we head into the holiday season. Kathryn

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Thanks so much. Just the fact that I can work is a blessing to me... as is this forum.

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@david1952

Dear Kwilbur,
Sounds like a tough time lately. Glad things are looking a little better. I too worry, but have trouble turning it off. I like the poet's quote, "it's a good thing the future only comes one day at a time!"
david1952

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David - what a great quote! My issue is that a suspicious node is in a place that a bronchoscopy or biopsy at the hospital can't reach. But I am feeling better - even looking into the future. I value these good, strong, times so much. Best to you, Kathryn

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@kwilbur

I haven't been contributing as much to this forum as I am in limbo about my lung condition. I spent half a day in the hospital expecting to have a biopsy of a nodule 9 mm - only to be sent home because the radiologist was afraid of hitting the wall of my lung and my having a collapsed lung. While at the hospital, I had another cscan done and the nodule had gotten small 7 mm , the size it was in June.

Oddly enough, I have stopped coughing up phlegm too - or very little. I was getting sick alot at the beginning of the school year which was treated with antiobiotics. Then I had the flu shot and I really don't know what is going on other than I do know I have bronchiecticus which is a constant.

I am able to keep up with a long school day, but don't do any work once I am home - about 6 p.m. Today I pressure washed my house - well with a light weight Home Depot system and a hose - and was able to keep up a strong pace for six hours. I only pray I stay on this path.

I know I have to remain vigilant but spending every day worrying is a waste of quality life. I was already in a mindset that I had lung cancer which now I truly doubt. It's not worth worrying about possible outcomes until they are a fact. I wish you all good health and stamina as we head into the holiday season. Kathryn

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Kathryn, as usual .. you are busy "counting your gratitudes" .. good for you! Truthfully .. all I have to do is look around me and I am made aware of just how blessed I really am .. there are indeed so many others so less fortunate .. each in different ways. I really try to keep that in mind. There are ways I have difficulties .. but there are SO many blessings .. why not focus on the blessings? Makes the day SO much brighter! As I say to my husband "Rainbows and Butterflies!" when he gets a bit grumpy! Hugs to you on this journey! Katherine

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@david1952

Dear Kwilbur,
Sounds like a tough time lately. Glad things are looking a little better. I too worry, but have trouble turning it off. I like the poet's quote, "it's a good thing the future only comes one day at a time!"
david1952

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I have Stage IV, Metastatic Breast Cancer. This not "curable" per my doctor and everything I have read. My father died at 53 from heart attack number 4. I always thought that would be my fate. Now I at least know the enemy and can work with my oncologist to figure out how to extend my life and make it as comfortable and productive as possible. The biggest positive of this journey is my husband and his support. He is really the only close family I have but he is my best friend and the love of my life. I hope and pray for all of you and I hope all of you have a support system. So important. Love to all.

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Wandering, I SO understand. My dear husband is on chemo .. Stage 4 .. not curable either .. and obviously I have this MAC .. but as with you two .. we live our lives as fully as possible and has happily as possible! My husband just got back from a "road trip" with our daughter to watch our grandson who is in his college senior year play his final game as quarterback for his football team. They drive 7 hours each way! This ends a nine year journey of road trips for the two of them .. a bittersweet trip for the two of them .. great talks and great fun! All a part of living our lives to the fullest while we can.

We also are each others best support system. As we say: Our kids love us .. our grandkids love us .. but as three in the morning .. It's just you and me Babe! That tells it all! You and I are indeed blessed to have that support system .. MANY do not. Are you aware there is a Mayo Clinic Connect for Breast Cancer? There you may find the same kind of wonderful support we have on our Forum for our MAC people?? Maybe check it out? https://connect.mayoclinic.org/group/breast-cancer/ Sending you a hug! Katherine

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@katemn

Wandering, I SO understand. My dear husband is on chemo .. Stage 4 .. not curable either .. and obviously I have this MAC .. but as with you two .. we live our lives as fully as possible and has happily as possible! My husband just got back from a "road trip" with our daughter to watch our grandson who is in his college senior year play his final game as quarterback for his football team. They drive 7 hours each way! This ends a nine year journey of road trips for the two of them .. a bittersweet trip for the two of them .. great talks and great fun! All a part of living our lives to the fullest while we can.

We also are each others best support system. As we say: Our kids love us .. our grandkids love us .. but as three in the morning .. It's just you and me Babe! That tells it all! You and I are indeed blessed to have that support system .. MANY do not. Are you aware there is a Mayo Clinic Connect for Breast Cancer? There you may find the same kind of wonderful support we have on our Forum for our MAC people?? Maybe check it out? https://connect.mayoclinic.org/group/breast-cancer/ Sending you a hug! Katherine

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Yes, I think I was on the breast cancer connect. Don't know what happened and I think I might not now be on the blog but I'll check on the link. We don't have any children and nobody from my family knows about me except my sister. For me that's the best thing - no need for everyone to worry. We have spent this summer in doctors offices, clinics, labs and hospitals. He had a stent and skin cancer surgery and I had my usual stuff. I was wondering how we would spend our time after we retired - didn't think we would be doing that but here we go.
Heading for Arizona on Friday for the winter. Right now it's 60 degrees in Montana. It's usually snowing by now.

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