(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.
@gggolfs, Hello GG, man this is a tough time for you. Virginia .. hmm .. would Florida be too far? Below is the info for Mayo Florida in case you might consider that. The contact information for Minnesota, Arizona and Florida can be found here http://mayocl.in/1mtmR63.
Also read the past pages of the post to find a :
1.GOOD Infectious Disease doctor locally. Just google it
2. call the various offices .. ask to speak to a nurse .. ask 'How many MAC patients has your doctor seen in the past 12 months?' If a NURSE in the office does not even KNOW what MAC is .. that is a pretty good tip off that office does NOT treat MAC patients!
3. Request an appointment with the BEST ID doctor locally you can find
4. I would collect AN/Y/ALL medical records I could get my hand on from ANY/ALL doctors you have seen. It may take them emailing you Authorizations for Release of Information .. BUT DO get started.
5. Having read ALL the back pages of this Forum .. done your 'due diligence' .. educating yourself .. you will NOW have a LONG page of questions and will KNOW exactly WHAT the ID doctor SHOULD be doing for you .. or NOT doing.
GG, hope the above helps .. feel free to ask any questions .. we are here for you! Hugs! Katherine
Linda, because our posts are in time sequence .. wish they were not! Wish the posts were all together related to a particular question or post .. that said .. WHO were you asking this question of? Best to start with a name so the person knows who the question is being asked of. Katherine
Sorry Katherine. That was in response to Terri's check up results. Linda
I think there's a greater connection between GERD and MAC meds... I've not heard those who are asympomatic having the problem
I am sure there is a connection between GERD and MAC meds. However, there is documented evidence of a high percentage of people who have been diagnosed with GERD also having a MAC diagnosis (not from the meds). I have also discovered that the incidence for MAC is higher with people who have pectus because of skeletal structure. I pray to the good God my son doesn't have MAC as he has lots of symptoms, and he was born with pectus. We did, however, have his repaired at Boston Children's in 1981. - Mother's guilt. Irene
@irene5, Irene, STOP! If all us mothers with adult children with various issues slit our wrists .. there might be few of us mothers left in the world!! I myself only gained 12 pound with a pregnancy because I was chasing around a toddler plus working .. when I produced an adult hyper active .. I also had mother's guilt until I realized the above! So join me in realizing we did our best!! Hugs! Katherine
BUT Your info was interesting .. something I was unaware of .. thanks for the new info .. anyone interested can check into:
Principles and Practice of Infectious Diseases https://books.google.com/books?isbn=1455748013
John E. Bennett, Raphael Dolin, Martin J. Blaser - 2014 - Communicable diseases
of macrophage activation to eliminate intracellular MAC.79 MACspecific T cells ... Studies have reported that 11% to 27% of individuals with MAC have pectus ...
Thank you Linda!
Unfortunately that does not indicate a clinical association between MAC & GERD. It is one of the areas in which no research has been done so any evidence is circumstantial (as is that many asymptomatic folks like me don't have GERD). The closest thing I've found is a NJH article mentioning that GERD may be a cause of MAC...again, without clinical research to prove the hypothosis.
That said, the important thing, I think, is whether the treatment for GERD changes for those with MAC. Anyone found research on that?
Someone posted that he or she went to a doctor at Mt Sinai Hospital in NY who seemed knowledgeable about MAC. Please mention the doctor's name again.Many thanks.
Boomer, Dr. Timothy Aksamit of Mayo Clinic, Rochester MN speaks all over the world on MAC .. and he told me he feels there is a connection between GERDS and MAC despite there not being proven research .. that statement is good enough for me.
Then recently Terri had this experience at National Jewish Health for MAC .. another "mecca" ..
@tdrell .. terri The reason MAC was found in my lungs when i had the bronchoscopy was that I have severe GERD and since it...NTM is in tap water....it had been aspirated into my lungs as I slept.
I think the two experiences give us a very good feel for not discounting GERDS being connected to MAC .. since there is very little money for researching MAC .. it results in very little clinical association/research to prove the hypothesis.
Since as Terri said .. the MAC RESULTS from the GERDS .. it ends up with continuing treatment for the GERDS .. and/or treatment for MAC. Katherine