What’s the youngest person to have MAC?
I’m 38 years old and tested positive for MAC just had my CT awaiting results. My immune system is normal and I have no lung disease prior and my PFT was normal 2 months ago. Anyone else have this infection at a younger age?
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
Not @scoop, but here it is:
https://www.ntminfo.org/wp-content/uploads/2019/09/Guide-for-Patients-with-NTM-Infections-2019-09.pdf
I suspect I probably have BE. I had recurrent bouts of bronchitis as a teenager that all but stopped in my 20’s and 30’s. It wasn’t until Covid that I had a true chest infection since then. Last December before my symptoms started I tested positive for Covid and influenza at the same time. In my mind maybe I had MAC and it was just colonized asymptomatic, then the covid flu combo caused my immune system to lose control of it?
@vegita182 there is a support group for those with BE/NTM under 50-ish. I could be a good additional resource for you. Check out the link for a calendar of support group meetings, and scroll to the one for under 50-ish. It looks like it is once a month.
https://connect.ntminfo.org/events/calendar
Thank you so much.
I’m 35 and was just diagnosed. Recently had my first child in September, went to the ER 9 days postpartum with chest pain and some signs of infection. Was treated for pneumonia but the chest pain lasted for about 3
months. Have struggled to sort out potential MAC symptoms from normal postpartum symptoms (e.g. night sweats) but at this point I am largely asymptomatic. My pulm wants me to start treatment regardless because of how my CT looks (though this is also atypical) - the MAC was found from biopsy because I haven’t even been able to cough up any sputum. I had the same question as you do, would be really interested to hear stories from other young and healthy folks because it seems bizarre.
Welcome to Mayo Connect - and our support group that can answer many of your questions!
When an atypical patient joins us, I always want to say "First, find a pulmonologist who is a MAC expert." This is not a negative statement about your doctor, MAC/NTM experts are rare because this is a very rare infection. Even many experienced pulmonologists only see a case rarely, and may not be familiar with many of the latest treatment standards and protocols. My first pulmo treated 27 cases in 27 years, and I thought "Oh, that's pretty good" - until I realized that I was getting more up-to-date info on Connect than from him.
Now I have a pulmonologist whose practice is about half people with Bronchiectasis or Cystic Fibrosis, and who is up-to-date on how to manage MAC - often without medication. If you are in a large metro area, you may be able to find a well-versed doc, or you may need a consult at National Jewish Health (NJH), Mayo, NYU Langone or a similar center of excellence.
Did the pulmonologist explain exactly why you should start the med regimen? Are you looking for a second opinion?