Anyone been mistakenly diagnosed with MAC Lung disease but not MAC?
I was diagnosed with MAC Lung disease 4 years ago due to findings on CT Scan and sputum cultures. However, recently hospitalized with pneumonia and a different Pulmonolgist did thorough research on my case and believes that I was misdiagnosed and don't have MAC. Just wondering if anyone else has had this to happen? Luckily, I chose not to get the extensive antibiotics treatment because I felt the treatment was worse than the disease. Would appreciate knowing if others have experienced this.
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Hi Linda,
I went to Mayo clinic last September. I do use nebulizer on and off. I do not mind be part of the study. I am talking to a my immunologist at stanford. Hopefully in the next 2 weeks I will have an answer. I have thought bout contacting the National Jewish Health.
Right now my pulmonologist has prescribed Azithromycin 500MLG for 5 days a week for 2 weeks and start the next one in 2 weeks. I will keep you posted.
Thanks,
Suzanne
Thank you
An Infectious Disease Dr. is your best bet. They seem to know more than a Pulmonologist. My Pulmonologist talks a lot to my Infectious Disease DR and they work closely together. Infectious Disease diagnoses and treats infection while the Pulmonologist treats the breathing problems and mucus production. The pulmonologist also got my airway clearance vest approved for insurance and keeps my asthma under control. He does my bronchoscopy when needed as well to wash the mucus out of my lungs.
A sputum sample will show MAC as well. At least mine did.
Mine did too but it doesn't all the time. Bronchoscopy is the only for sure way
Thanks, that's probably true I haven't been able to see a pulmonolgist since the negative cultures but I have an appointment next month and will find out what he recommends.
Thanks for your response.
Or a surgical lung biopsy
Hello everyone,
I was recommend to start treatment with azithromycin and ethambutol. One of my Pulmonologist prescribed 1 tablet of zithromycin (500mg )for 5 days a week and start ethambutoL 400 mg tablet to take 2 tablets (800 mg total) by mouth daily, 2 weeks after starting azithromycin.
My Infectious Disease specialist suggests azithromycin either at (250 mg daily or 500 mg ) 3x/week and ethambutol (15 mg/kg/day or 25 mg)/kg 3x/week.
I am very confused and nervous about the right dosage. So I contacted my Pulmonologist at Mayo Clinic. Whom originally when I meet last September did not think I should be taking the medications. He Suggested airway cleansing and sinus rinse with salt water and use a nasal spray.
I only did the sinus rinse with salt water for a few months, I hardly used the nasal spray, I wonder if that would had helped my situation?
I use the nablizer at least 5 times a week. I am pushing myself to do it twice a day/7 days a week as prescribed.
I am planning to start the medication as soon as I hear back from my Mayo Clinic Pulmonologist. I admit I am very nervous . 😟 😰
Do you think I should do a Bronchoscopy first? My last several septum test has been MAC positive. My last lung CT was last July. I have done so many CT scans, nervous to do more!!! ( Total CT scans since 12/22 / 3 times)
Since 2000/ 26 CT scans !!! Any time I go to emergency room they order a CT scan. 😭😭😭
Good news is they have built a new CT scans with much less exposure to radiation.
This is extremely hard not knowing what step I should be taking next, not even knowing what is the right medication dosage???
Has anyone gone through the same experience?
What about taking probiotics while taking the big 3? Did anyone took or is taking probiotics with taking the big 3 ? And if so how often? By the way they do not do big 3 anymore! I guess is the big 2 now... lol
I was also prescribed the airway clearance vest, my co-pay is extremely high, but if it works it is definitely worth it. Please let me know your experience with airway clearance? Does it actually help?
I greatly appreciate all your suggestions and experience on what to do and what to eat while on the medications? I have an appointment with my nutritionist tomorrow morning, so hopefully she would guide me on the right path.:)
This feels like a long Journey. I hope we all get better soon.
Thank you for your support.
Suzanne
The trend and studies are moving to less dosages. Daily AZ is pretty tough on the GI. Much prefer MWF myself
Please let us know what your Mayo Clinic pulmonolgist tells you about the nasal spray.
I signed up for a Clinical Trial for MAC Lung disease 2 years ago but declined to do it when it was moved out of Dallas. I'm not sure but I think the Clinical trial was testing a spray of some sort but I'm not sure about that.
Hopefully, a better form of treatment will be developed than taking all those antibiotics for such a long period of time.
Good luck with your treatment and health.
Good morning Linda,
Did you see my recent post?