(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.
I may ask about the alternating meds in the future.
Greetings all!
Does anyone know if the Conference in Washington, DC is posting their lectures on the internet?
David
I will ask my doctor when i go back about checking my hearing! I may also see if i could change the time i've been taking my antibiotic from night time to morning or afternoon. The pharmacologist is the one who recommended to take at night so i would sleep through the side effects, but I think the side effect for me is trouble to go to sleep. They want be checking my vision again for another 6 months unless i start having a problem with my vision. I hope and pray it will not change!
Thank you for your info!
Thank you very much Katherine for your information!
anr38. The pharmacologist told me the same but I somehow (almost a year ago) figured out that Rifampin kept me awake at night. I switched it to AM, an hour before breakfast for full absorption, and then slept much better.
Best wishes!!
@lindam272, you questioned about asking your ID doc for another CAT scan since it's been over 6 months since last scan. I agree with @katemn who mentioned the concern for radiation. Many people, unaware of the radiation risk, push for tests. My pulmonologist alternates each year, one year x-rays and the next CAT scans. He is concerned about the radiation in both x-rays and CAT scans, recognizing they are the best, least invasive diagnostic tool there is. Also, don't be surprised if it appears in your lungs that the NTM has 'shrunk' but then appears somewhere else ... my pulmonologist says that the nature of the disease.
Here's an interesting article ... "Should you worry about the radiation from CT scans?"
https://www.washingtonpost.com/national/health-science/how-much-to-worry-about-the-radiation-from-ct-scans/2016/01/04/8dfb80cc-8a30-11e5-be39-0034bb576eee_story.html?utm_term=.0fbe51228da7
Hope you are feeling well.
Paula
There is simply too little research being conducted on this growing epidemic...and I believe that dearth of attention will continue until someone in Congress or a celebrity get it and go public. Big sigh...
PLEASE PLEASE PLEASE PLEASE.....take me off your discussion email list. I have tried everything to block the emails...divert them etc. and they still fill up my inbox daily. I DO NOT WANT TO READ ABOUT THIS.
Ruth Van Dyne
@ruhbesb. I think you have to unsubscribe. You should contact Mayo Clinic Connect on how to do it.
@ruhdesb; at the bottom any email you receive, click unsubscribe, go to the tab 'account settings', click edit, you will find unsubscribe from all email notifications (I hope this is useful).