New Diagnosis of MAC/MAI & I'm scared
Hi, I am new to this site. I just got the results of my broncoscopy a week ago. First I was told I had Staph Aureus in my lungs & was put on Levaquin X 10 days. OK, Now she tells me I had MAI & I think the other one is MAC. Anyway, My pulmonologist said we are waiting for the sensitivity test to see if the bacteria in my sputum are sensitive to the antibiotics....or not....since now some strains are resistant. My name is Sue from Oregon and I am 61 years old with Sjogren's Syndrome, Rheumatoid Arthritis, Bronchiectasis, and now THIS. My RA & bronchiectasis are extensive with a lot of coughing and I am on a biologic immunosuppressive drug, infusion, for the RA. I read several posts at this site, looked up the side effects of the 3 meds my pulmonologist said she will put me on, scheduled an eye and hearing exam. This is scarey!!!! I'm already weary of my life having been turned upsidown in the last 4 years with my health struggles. (On SS disability now) I talk with a clinical psychologist every other week & she is helpful. Is it really helpful to talk about it online? Or does it just make one ruminate about it all the more? I'm not sure which it is. Please let me know if it has helped you cope, or not. Thanks.
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Laura34. I have been taking the Amikacin/ Arikayce since last October. I have been taking it every other day with literally no side effects. At the daily dose I began to loose my voice so my pulmonologist changed me to every other day. I am not on the big 3 because 2 of those drugs affect my heart rate adversely and my doc felt I was not able to tolerate them. I was scheduled for a ct in June but doc has said we will wait until August because of the corona virus. At last ct scan I have nodules and 3 cavitation lesions
Sounder27- good to hear you haven’t experienced any side effects. I will definitely mention it to my current doctor to see what they say especially since the current antibiotics I have been on for almost a year and a half now don’t seem to be helping much. I would love to hear how your next CT goes since being on the amikacin.
@windwalker888 @irene5 I too share your thumb pain! Just had another injection it doesn’t keep me awake at night. I severed a major tendon years ago, snow skiing, and had emergency repair surgery then. Now it’s arthritis, for which I have a genetic predisposition. (If it’s not one thing, it’s your mother.)
@brigby You are definitely funny! My mom always said I would have “old lady“ hands because I cleaned so much, and my hands were always washing dishes in really hot water. By golly she was right! I took her for a knuckle replacement before she died in 1995. That helped her a lot. She couldn’t even open her cabinets. My hands hurt all the time. I believe now my mom and aunt both had MAC. So yes, if it isn’t one thing, it’s your mother! That’s a good one! I needed a good laugh. Thank you. irene5
Laura34. I will definitely post my ct results. I am hoping for great improvement since my coughing has quieted down and I am not producing much mucus anymore.
@sounder27 I am very encouraged by your comment about Arikayce. I was supposed to start on Arikayce right when Covid19 hit. Since someone has to come to your house in the beginning, and my family feared I would end up in the hospital, it was decided I would stick to the Big 3 and wait a bit to start the Arikayce . However, for me the Arikayce is in addition to the Big 3. ( I only have to be able to tolerate and continue two of the Big 3 for the trial). Thank you. I am encouraged by your Arikayce comments. irene5
@irene5 Hi Irene! I hate that the covid put the skids on your arikayce. I would think it would be similar to the inhaled tobramycin treatment. That did not take anybody to show me the ropes on how to do it. Isn't it like nebulizing anything else like saline or albuterol? @heathert Heather, what do you have to say about it? If it is different, then couldn't you do it with a youtube video?
@sounder27 Hi there! Did you have to have instruction in person by a healthcare worker to use your Arikayce? Is it different from nebulizing any other med? Thnx!
Kate, that is funny that you mentioned your fingers getting 'locked', mine has done the same. I figured it was due to dehydration of something.
@laura34, Hi Laura. How long have you been on the Big 3? I had good success without going on them. You can see how I was treated if you click on my picture icon. I like to point that out sometimes to let people know that there are other ways to treat MAC besides the Big 3. It will all depend on your susceptibility test of course. Maybe you can speak to your dr about that.