(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.

@Paula_MAC2007

I was diagnosed with MAC in Feb 2008 (after having intermittent symptoms for 3 years that got progressively worse). For 4 yrs, 3 months (Feb 2008 - April 2012), I was on the 3 standard drugs for MAC . I had some side effects from the drugs but gradually they went away or I learned how to deal with them. If my routine got out of whack (like on vacation) I suffered.

Over the years, I grew to feel like my old self - although as a high energy person, I was somewhat sluggish from the medication. Last April, I negotiated with my pulmonologist to go off the drugs. What a relief! Was like a weight had been lifted . . . I felt much lighter and less sluggish. While my MAC was not gone, my lesions had shrunk over the years of antibiotics. I considered the MAC as hibernating or resting!

Eight months later (December 2012) I began experiencing the cough (which at times results in spasms) and tiredness. Since Feb, I have been on two different antibiotics from my Internist - to rule out a severe sinus infection. No dice! Yesterday (March 2013) I saw my pulmonologist who, before assuming it is MAC and resuming the meds, wants to do a lung lavage and CT scan. Will do this within the next two weeks.

Incidentally, my Internist did a lot of blood workup recently and my Vitamin D is very low. Am now taking 50,000 IU for 12 weeks and then repeat the tests. My pulmonologist yesterday mentioned there is some connection between Vitamin D and lung issues but it's not real concrete yet.

So my MAC appears to no longer be 'resting'.

I will follow this blog with great interest. I live in Wisconsin, in the part of the upper Midwest where MAC is found. Yet MAC is not found in some other Great Lake states. Sure is a mystery.

I WOULD LOVE TO GET IN A STUDY WITH OTHERS WITH MAC!!!!!

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I have recently been diagnosed with MAC.. Interesting... my Vit D level has been very low and I have just been prescribed 50,000 units one time a week. Did your Vit D level return to normal after this regiment? I am sorry to hear your MAC has returned.

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@windwalker

@jasmine321 Hi Jasmine, welcome to our Connect group. Well, that is certainly disheartening news after having been on those antibiotics for a year. I believe you when you say you have mac again, but I am curious how your dr. got such a fast diagnosis? It takes 6-8 weeks to culture a sputem sample and you mentioned that you had the sputem test done last week. Have you had a chance to read over some of our older posts or read our topics in the Discussion Board? It is located on the 'Mac and Bronchiectasis' home page. There is a wealth of info in our threads (conversations). My next reply to you will be about lavages.

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I submitted sputum samples for sputum culture and AFB Friday, then the doctor called me the following Thursday. He said the culture grew staphylococcus aureus. He put me on Levofloxacin for 7 days. He also said it looks like another organism is growing, could be MAC. I have another appointment with him on Nov 9. I will know more.

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@ameliar

I have recently been diagnosed with MAC.. Interesting... my Vit D level has been very low and I have just been prescribed 50,000 units one time a week. Did your Vit D level return to normal after this regiment? I am sorry to hear your MAC has returned.

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Yes, my Vit D was low and my doctor prescribed Vit D with calcium. My level is now normal.

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@irene5

@windwalker888 Terri I had lavage done - no success for MAC removal, but I am just one person.

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@irene5 Hi Irene! How are you doing?

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@jasmine321

I submitted sputum samples for sputum culture and AFB Friday, then the doctor called me the following Thursday. He said the culture grew staphylococcus aureus. He put me on Levofloxacin for 7 days. He also said it looks like another organism is growing, could be MAC. I have another appointment with him on Nov 9. I will know more.

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@jasmine321 Please keep us posted.

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@irene5

@windwalker888 Terri I had lavage done - no success for MAC removal, but I am just one person.

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@irene5 Hi Irene. How many of the lavage procedures did you get?

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@windwalker

@irene5 Hi Irene. How many of the lavage procedures did you get?

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@windwalker888 Since they aren’t a “walk in the park” for me, the ID doctor and my pulmonologist are debating a second one. ( But at the same time they are insisting on it). I’ll know more sometime in November.

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@windwalker

@irene5 Hi Irene! How are you doing?

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@windwalker888 I tried sending you a private message, but it didn’t go through. Suggestion? Irene

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@irene5 I think Terri's handle is @windwalker not @windwalker888. When you start typing the first part of the handle, you should see two options. One shows Terri M. Volunteer Mentor and the other just shows windwalker888. You need to pick the former. Maybe that's why your private message didn't go through?

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@ling123 Thank you sooo much Ling. FYI our first Chinese child (Yu Chun) is getting married on Saturday. She’s so little (4’7” and her fiancé is a “very tall glass of water” at just under 6 feet. She is a teacher for children with autism, and he is a math teacher at a private school of mostly Chinese international children. Praying that MAC leaves me alone that day!

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