Non treatment of MAC
Does anyone know what are the disadvantage of NOT being treated for MAC?
In February 2023 I started taking 3 antibiotics 3 times a day but by September 2023 I stopped taking them. One of the antibiotic was causing vision loss. It was mandatory that all 3 meds had to to taken together (all or none) for at least one year. Results of CT compared from May 2023 & August 2023 indicated that additional New nodes or spots were present. So it seems that the treatment wasn't working.
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Wow! That is encouraging. I have an appointment with my ID Dr. tomorrow, I will relay that information. I have Tricare For Life. Express Scripts is their agent, this medication requires TC for L pre-approval. My 20 yrs military service is the source of all my lung problems. I feel betrayed by their denial. If my Dr. doesn't get an appeal, the Govenor of my state is ex-military Navy as I was, I will contact him.
Thanks
Don
I was diagnosed in 2007 with Bronchiectasis and in April 2020 with Mac. I have not taken any antibodics. About 6 months ago I had 400 Colonies and I was smear positive. I started working really hard at airway clearance 3 times a day. My latest sputum culture from National Jewish showed 40 colonies and I was smear negative. I really believe airway clearance is the key. I use 7% Saline, the VEST and the Aerobika. I also do active cycle breathing. I am in another support group with over 4000 members and there are many people who are doing well with just airway clearance.
With all due respect, I can and do disagree.....especially for myself and the fact that without lungs, sight and hearing are mute. The post I was replying to ask "for any disadvantages" and that's what I replied with. I as well have consulted with NJH along with my Chief Pulmonologist and ID's. All involved have agreed that treatment should be started sooner than later. Best wishes to you and what works for you.
I am currently at NJH - it is snowing in Denver! I was told there is a good chance that I have built up a resistance to the meds. My pulmonologist back home took me off the meds 3 months ago to give my body a rest. My doctor at NJH told me Friday not to start taking them again right now. As I said, I am not telling you or anyone what to do but like you are deciding for yourself, I will follow the doctor’s recommendation here at NJH. I was diagnosed 4 years ago and started treatment then. Four years on the three meds.
I agree that airway clearance with 7% does help and can keep MAC under control for some, maybe not for everyone. Many people on this forum say so from their personal experience. My MAC has not showed up on my last sputum samples (including a three day collection at NJH). I am not have not been on antibiotics. Everyone is different!
Thanks for your thoughts. My cultures are negative. Saw my pulmonologist yesterday and he said yes my ct isn't worst. Will continue to monitor every 6 mo due to the amount of nodules i have. Making sure that they are not cancerous. I had neck cancer so i worry about getting another cancer. i thought the meds would clear it all but i was wrong. Need to enjoy my life and continue the airway clearance to keep infection from growing.
Hi Sue
Met my pulmonologist yesterday and had a good conversation about my lungs. He told me that yes my ct still showed the infection but culture are negative. Like you mentioned as long as i am not feeling sick we continue to monitor, having ct every 6 mo and see what changes are happening or not. He says that i have lots of nodules, they wax and wane, but need to follow up in those due to my neck cancer. I worry about that. He told me to enjoy my life and do the airway clearance, excercise, my albuteral, and use my flovent when i feel wheezing to clear it. I just needed to realize that this will be with me for the rest of my life. I thought the meds would eliminate it.
Glad to be in this group to be able to share how we feel without being judged. Thanks for your thoughts. On my way to play golf and walk its my excercise! Life is good and all will be well😘
Miriam I am so happy for you. If you have wheezing at times, does that mean you also have asthma? If so, there is a new protocol for treatment that replaces the albuterol nebs and [at least for me] 95% of the need for a rescue inhaler.
It is called Symbicort. It is a combination of formotorol and budosenide.
Sue
Donna,
Has your doctor checked your thyroid level? I was experiencing fatigue, hot flashes, severe night sweats. I thought it was the MAC worsening, but it turns out that my prescription for levothyroxine was too high. Apparently, one’s need can change over the years. It’s improved now that the prescription has been reduced; the night sweats aren’t gone, but they are reduced. My blood pressure is normal (whereas it had been very low). Good luck!
Thank you. My thyroid has been checked many times, and they always say it is normal, even though I have symptoms to say otherwise. But I appreciate your note.