(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 have started preparing him mid-morning, mid afternoon and evening snacks. It is still very surprising, but he eats very well. I search for snacks on Pinterest and other sites but seeing a dietician is also a very good idea. Thank you.
So true...
@heathert, You are so very welcome. I appreciate that you (and others) are regulars on here. You ALL are part the success here that makes this a great community. You all are so good about catching newcomers that I miss and add good input with the information. I keep hoping that our conversations change to NEW therapies that work, or I AM CURED forever!! I pray that stem cell therapy gets to the point where we can reverse the damage of bronchiectasis. I am thinking of going to the World NTM conference in D.C. again this July to see if any new info is out there. -Terri
@lauriefrancis Hi there. Prayers for Nina are still on. Your family is never far from my thoughts. -Terri
@windwalker Oh I AM CURED FOREVER would be wonderful as we would all be cured on here, hope I see the day soon! Let us know how the NTM confrence in D.C. goes, fingers crossed.
@suzie2017 Hi Suzie. If your husband goes into pulmonary rehab ,a nutritionist comes with it. You can add ice-cream to powdered protein shakes to pack on some calories. Add mayonnaise or sour cream to mashed potatoes and cheese on top! People with breathing deficits require 10 times more calories as healthy people. We burn more just trying to breathe. (coughing a lot will also burn up your calories) We have to fatten your man up!
@flib Hi there! You already are nebulizing sodium chloride. Here is your post from April 24: " I'm eighty-one. I use a nebulizer with a saline solution my doctor prescribed. It really helps. I only did one antibiotic for less than half a year and loss hearing as a result. Amazon has an easy to use nebulizer, Light to hold in the hand and it's quiet. It's an ultra sonic not a compressor. It cost about 26 dollars. I'm also on oxygen at night. A pain in the neck but I'm use to it now and it does make a difference. I've had mac and bronc since 2010 and I am still functioning. I drive, run errands, visit run my own life. ." NOTE: saline and sodium chloride are the same thing. It is a salt solution. This solution is beneficial because it thins the mucous making it easier to get up, plus it makes it inhospitable to bacteria. You probably grew up gargling warm salt water for a sore throat and had a cold coming on. By doing so, it was soothing and killed germs. It is the same concept for your lungs. I hope you are continuing with using it. How are you doing?
My husband has been in pulmonary/cardiac rehab for about 6 months and no one has said anything about a nutrionist. I really like that idea. I have been loading him up with calories. Last night we had chili with sour cream and cheese and also Texas Toast. He has a dish of ice cream every night. He eats really well but the pounds keep coming off. He is doing well over the weekend so far. Our son came in from Colorado to surprise him. Thank you for the good tips. Hope you are doing well this weekend also.
Thank you so much. It takes a while to master the vocabulary.
@flib It Does. So, are you still nebulizing your saline? Are you doing alright?