Why Dr has NOT prescribed me Rifampin for MAC/NTM?
Good Afternoon Village!
I was recently diagnosed with MAC I have a 3.7 CM hole in my lung. My infectious disease doctor started me on my medication about a month ago; ethambutol and azithromycin PLUS my doctor will be putting me on an inhaler that's medicated but it's very expensive so I have to wait until I'm on these meds for a few months (I'm not sure what that's called). He has not mentioned putting me on Rifampin or even mention that drug. I'm just curious what the reason would be since it seems everyone else is on all three of these and I'm on two of them. My doctor did tell me that my case is mild although I do have a hole in my lung?!?! My doctor does have extremely great reviews, and has said he treats a lot of Mac patients but I'm just curious if anyone else has only been put on a couple drugs and not all three? Like I said I'm supposed to get the inhaler too in a few months. If anyone has any information or similar experience please let me know. I appreciate it 😊!!! Thank you all-
Angela
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I think you will be fine with that cocktail! God bless you real well! ( Irene)
I started Arikayce right away because I have a lung cavity with MAC. I was quoted the same cost and pay nothing because of the Assistance program. Now on it for 12 months and have tested negative for the last 10. Also on the Big 3. So it appears to work.
Yay!!! So happy for you!
There is currently a clinical trial on taking three antibiotics versus taking only two for MAC lung disease. The two antibiotics protocol leaves off rifampin. Many doctors feel that this is sufficient to prevent resistance and eradicate disease. To learn more about this study you can go to this link:
https://mac2v3study.org/
Best,
Linda Esposito
I am about 4 1/2 months into treatment with the Big 3. MAI along with Aspergillis Niger were discovered 8/2022. Treatment started 11/22. My most recent sputum showed Aspergillis Fumigatus, still waiting on the AFB. My doctor doesn’t seem concerned about the Aspergillis, but I certainly am based on what I’ve read. Did Aspergillis ever show up for you previously, or just after you MAC treatment was complete?
Aspergillosis fumagatos showed up on a biopsy 8/2/2022 after a “minimally” invasive robotic surgery. Unfortunately, my lungs were so fragile I had a pneumothorax after surgery and a chest hemorrhage after they took the tube out. I was at UMASS for two weeks. I was on Vfend - switched to Cresemba and now back on Vfend. Insurance won’t cover the Cresemba in 2023. They covered it in 2022. - so crazy. Not a fan of all this. They discovered MAC was gone prior to this (6/2022 with a bronchoscopy). Apparently it is not uncommon to get rid of one thing only to replace it with something else. The aspergillosis is apparently easier to treat than MAC. My diagnosis was invasive aspergillosis with pneumonia. The joy of it all.
Thanks for sharing your story, you have a great attitude! One more question, after having a bronchoscopy in June 22 why did they feel the need to do the robotic guided biopsy in August 22?
Irene, we are having parallel experiences. After years of MAC, big 3, amikacin, arikayce, etc, I too was diagnosed with a fungal infection in 2022 after developing systems in March. I started voriconizole in November. Dr's at NJH want to preform lobectomy this year. I'm working on a 3rd opinion now. Also developed some recent tachycardia so a Cardiologist is scheduled in May. I'm trying to hold off until after May when I turn 65 and get Medicare. I also had a GSD for 14 years until last month, father time caught up to her. I miss her.
I know right! I’m such a great guinea pig. I actually had one in March too. I stopped breathing twice so they scrapped that one. The reason for the third one was because I had a 7mm nodule, and lung cancer runs in my nonsmoking family. They wanted to biopsy it to see exactly what was cooking. Plus, I had so much more stuff in my right and left lungs that was concerning. I also have a rare azygos ( sp) fissure which is a wonderful teaching moment thing. Lol. I am not a spitting kind of gal so sputum production is a waste of time for anyone trying to get that from me. They have decided not to do bronchoscopy procedures on me for a long time and just do the Vfend medication and CT scans. As far as my attitude I am positive most of the time. It takes as much effort to be positive as it does to be negative. Admittedly I have had a few pity parties! Crying wears me out and gives me a headache so I try not to do that too often. I figure the good God’s got this so I try not to worry. My kids and grandbabies hover way too much, but they keep me putting one foot in front of the other.
Oh my goodness! I don’t know what I would do without my Nala and Simba. We had five until a few years ago ( 3 GSD’s and 2 labs). When they died my daughter insisted I get a puppy - and everyone needs someone so we went back to New Hampshire two months later and got Simba’s sister. (Nala). I have face planted a few times - Simba is a big boy, and I’m 73 and weigh my age, but they give me reason to get up and for my husband of 53 years with sarcoid, dementia, and Parkinson’s to get up as well. Dog is God spelled backwards. You should get a puppy. My heart is having issues as well. We must be sisters. This growing up thing is highly overrated! I started on Vfend in August. My eyes still go buggy for a bit every day, but my levels are where they are supposed to be. You take care- but get a puppy! You won’t regret it!