(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.
<br><br><br><br><br>Indeed, we all will. Thank God for all of you.<br> <br><br>
<br><br><br><br><br>Ditto from me Katherine. <br> <br><br>
<br><br><br><br><br>Hi there. Just saw this post tonight. Wondering how you are doing <br>now? -Terri M.<br> <br><br>
Got it, Windwalker. I totally understand. 🙂
Tk u so much. I know I have to start on meds soon. In the process of getting new Mac dr.
In Toronto the system sucks. U have to wait. Hopefully I can get in sooner for new Dr, but u r right I know I have to start meds...
@nannette and @windwalker....Nan, did you have silent acid reflux or heartburn? I have no heartburn. The only thing I have is some clearing of my throat and maybe a little extra saliva/acid coming to my throat sometimes...I didn't know if that was due to bronchiectasis or not, because this is all new to me.
@windwalker....how long did it take for your symptoms to clear? Were you put on medicine for acid reflux or just diet change? Did you have a scope done again, or how did you know yours cleared? Thank you!
I have been doing some researching...and some firm thoughts are that PPI's don't work on people with silent acid reflux. Thanks for your replies in advance. Amy
Amy
I was told I had silent reflux for a full year. PPIs, diet, elevated head of bed didn't change my throat clearing. Had the gold standard test for reflux at Mayo. 24 hour Impedence test. I do NOT have ant reflux. I clear my throats and have tons of mucous. My MAC is supposedly gone. Now theyre saying it's inflamation in my nose. My sinuses are healthy - very honestly, tons of people have it. I don't think they really know why.
What do others think?
Kay S
@katemn, Katherine, I am sending you prayers.
Rosemary
Katherine, I hope you are feeling better and the Mayo is taking good care of you! I really appreciate all that you do for our little MAC forum! Take care of keep us posted when you are up to it! Barb
<br><br><br><br><br>Hi Amy. I only took the PPI for several weeks and the burning in my <br>esophagus went away. I still take some from time to time for stomach issues, but <br>not very often. That was several years ago. I have not been re-scoped since <br>then. I had a swallow test and a 24 hr acid level test done last Dec. Not <br>totally sure if they can tell from those tests or not. Those tests were part of <br>the pre-qual transplant panal. I feel like my GERD is gone or minimal, but don't <br>know that for a fact it is gone.<br> <br><br>