(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.
@nick52, Thank you, I will!
@nick52, Hey Nicole, how did it go today at the specialist?
Pfists, i don’t know if you got my message “ how rhe test is done” but the test is call video deglutition and you can see how the test is done on google. The gave you different texture like cookie with barium, pablum with barium , apple sauce with barium, juice with barium, thick liquid with barium and the x ray is on the left side (here) like a video and the radiologist can see how the swallowing is functionning. If you hav aspiration they will see it. It is the only test that can confirm “aspiration”. Is this clear enough for you. If you have a question do not hesitate to make your request.
I forgot to tell you that I ask the radiologist and my infectiologue about aspiring acid reflux to the lung and he said yes. Aspiration is the cause of bronchiectasis. I had read that but no one had confirm it but the radiologist did. If you eat mucus forming food you will have more expose or have more chances to pneumonia my dctor said. If you have a lot of reflux have you ever consider having NAET treatment. Those treatment are amazing Windwalker. I will give you an exemple of one of my treatment. I couldn’t eat butter anymore because I was getting to much mucus reflux and sputum so I switch to coconut oil, when I went for my allergy test I score 10 on butter (at 4 it is considered severe) yes 10! I had the treatment and now butter doesn’t affect me at all. The beauty of the treatment is you don’t need to stop eating it. I am looking forward to meet you when I get to Florida.
I hav never taken antibiotics for the MAC
Dear Windwalker,
Today I met the orthophonist who is the specialist for swallow abnormalities. On the xrays they could see both tube the one that goes into the stomack and the one into my lungs. She said they were able to see the clear liquid going down a bit in the lung
tube before the swallowing process has done its job. So to prevent liquid to get into the lungs I will have to thicken my clear liquid because this is the problem (clear liquid not thick) so I have to thicken at the NECTAR LEVEL which mean a bit thick like
a Yop (liquid yogourt). The thickener is called ThickenUp (clear) it work really well and doesn’t change the taste of whatever I drink. I need to be careful eating a balance acid alkaline food to keep the ph balanced. The weakness is at the back of my tongue
on the right so I can do exercices as seen on the video I have posted on this site on SWALLOWING EXERCICES. The ThickenUp is a must not to aspirate my liquid.
I also have to have an MRI of the brain because aspiration can be caused by a neurology problem. In my case the doctor radiologist think it is due to my TMJ surgery in 1985 in Quebec or 1986 in Portland Maine. In 1986 they had to cut the outside of my throat
to prevent infections.
So we need to check if it is neurology or the surgery. I will keep you posted.
To me it make a lot of sense because of all the problem I had since that surgery.
Windwalker, if you email me at nickyves52@hotmail.com I will send you a photo of the ThickenUp because there is 2 kind that I saw at the pharmacy today.
Sorry it is nicyves52@hotmail.com. (No k)
@nick52, Wow, Nicole! This is all incredibly interesting. Swallowing issues adds another facet to the causes of lung diseases, especially bronchiectasis. Thank you for sharing this with the group. This may be a topic for some on this thread to ask their doctors about; particularly those with reoccurring lung infections. how often do you do your exercises?
@nick52 All interesting info. Yes, I look forward to meeting you too some day as well.