(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 really appreciate this group and have learned a lot about my MAC. I also have Bronchiectasis. Is there a chat group for people with that?
Hugs from David
Not sure about dividing up drug. I take 4 ethambutol at a time and asked both doctor and pharmacist if I could divide it. Both checked the literature and found no permission to do this. They said it needs to hit the bloodstream at full strength. A weak dose may not knock out the bacteria and let it morph into a different bacteria that resists the medicine.
David
@david1952, David, our group is ALSO labeled "Bronchiectasis" .. AND since I have been stable from the MAC since May 2014 .. I really feel I am now primarily dealing with the affects of my Bronchiectasis .. so REALLY wish more of our group with Bronchiectasis would jump in and share symptoms .. tips .. survival techniques .. what their doctors have told them etc! I would LOVE this!
My Dr. Aksamit told me that MAC and Bronchiectasis frequently go hand in hand .. that it is really not know which comes first .. chicken/egg thing. Do we get Bronchiectasis first .. then it becomes a breeding ground for the mycobacterium .. OR do we get MAC and the Bronchiectasis comes second. They just don't know.
I have been told that my Bronchiectasis is not severe yet so I am very grateful .. BUT it is a real pain in the batooty! I cough a LOT .. especially for some reason in enclosed spaces like cabs/autos/buses .. theatres .. restaurant booths. The result is CONSTANTLY kind people offering me lozenges if I have forgotten to tell them "I have a lung condition .. but it is NOT contagious" .. my usual refrain It really becomes terribly embarrassing because it is constant! I also cough a lot when I lie down to go to sleep at night. But I keep reminding myself of my "gratitudes" .. how it could be SO much worse!
So David, hope others with Bronchiectasis jump in with their thoughts etc. I'd really like that! I'd love more activity about Bronchiectasis. Hugs! Katherie
Hi Terry
Rifampin messed w my sleep. I take it in AM 1 hr before breakfast now. You gevused to it in 3-4 weeks, at least I did. Also, it keeps Synthroid from absorbing so I got very hypo thyroid.
Also, I got irregular heartbeats and was VERY shaky and nervous at first. I think Azithromycin plus just being nervous when you first find out you have MAC all contribute.
Try to give it time, eat healthy, get a little exercise, stay busy with other things......it gets better, promise. I cried the first week on meds. I'm pretty ok now....
KayS
@david1952, David, thank you SO much for jumping in .. this is a GREAT piece of information for our Forum! In fact I am going to add it to my notes! Good job! Hugs to you! Katherine
@kaystrand, Good advice Kay .. you all know just how tough it is in the beginning .. but at least Terry found our community of great people .. she definitely no longer has to feel so alone! Hugs to you! Katherine
Terry, I am 2 days of 7 into my workup at National Jewish Health. I will always be grateful I came!! The place is amazing! Every one who works there are caring.....I am treated as a person. The testing ...example CAT scans are the most thorough I have had! And the results...which you can access thru the patient portal online site...are so thorough and detailed I wish all radiologists could come and learn how to be so exacting.
I stayed at Residence Inn downtown who has a free shuttle to Denver Jewish and reasonable special rates for clinic patients.I will stay at a Staybridge Suites next week....again...special rates and free shuttle.
Be sure to bring along CDs of tests even if you had them mailed
A thick folder will be sent with info....be sure to filll out and send in what is needed....and bring the folder and empty notebook with
More after January 16. Terri d
@tdrell, Terri, thanks for all the good advice .. as your usual! Keep us posted on how you do on our own Forum so our people will know how you are doing!
Terry is now posting there! https://connect.mayoclinic.org/discussion/mycobacterium-avium-complex-pulmonary-disease-macmai/?pg=20
Hugs! Katherine
Terry
Hope someone can send you the link from Dr Huitt at NJ on how to take meds. She says to take all Ethambutol at the same time to get it into your system each day. Same with Rifampin. I take R in am and E and Z in evening. All on empty stomach for absorption!
Others can weigh in on this.
KayS
I would be interested in that link as well. The woman in my office who has the same disease takes her meds separately because they are so hard on the system so that's what I've been doing. I seem to tolerate the Ethambutol well so will take those together tomorrow and will do the same with the Rifampin, taking them as you do. The Ethambutol is supposed to be taken with a snack or light meal according to the literature that comes with the rx.