What causes the bacteria to grow in some people and not other?

Posted by 1478 @1478, Jan 11, 2018

My mother was just diagnosed with MAC, having "the cough" for awhile now. After researching the internet all over the world on this bacteria culprit, I am trying to find out why the cilia in the lungs get damaged and allow this bacteria to invade. This bacteria is everywhere (water,soil) mostly. What has happened that people are getting this a lot NOW? Can anyone answer these three questions so that we may link WHY this bacteria may be getting stronger for some, please. There has been a 30% increase of the diagnosis of MAC in the last 20 years. It seems to be a large number of small, petite white woman, getting diagnosed between the ages of 61-17, in the little bit of studies that have done. I want to find the connection! I am also in the medical field, and don't want MAC when I get to 61 years old. (10 years)

Have you ever smoked? how long? when did you quit?
Have you ever been an RN, or worked in the medical field?
Have you ever had whooping cough?
What part of the country were you raised?

Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.

Welcome to the group! I find that certain foods cause the flood of phlegm...experiment and find out what your usual suspects are...

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@jensfcv

New to group....I have been diagnosed with mild bronchiectasis-also acid reflux....this has been ongoing for last 10 years. Gave up smoking 35 years ago. Worked in dental field, also in medical field. Had every childhood diseases known- born in England just after war...damp climate. Began with pancreatic issues five years ago and now after several tests I have been diagnosed with a mutant gene for Cystic Fibrosis. I don't have tCF just the gene.....perhaps this might explain some of my long term problems....always wondered why "mild" bronchiectasis caused such amounts of flem.

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Welcome, @jensfcv. I'm bringing @lindam272 who has atypical cystic fibrosis as well as MAC.
Jen, how do you manage the phlegm?

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@jensfcv

New to group....I have been diagnosed with mild bronchiectasis-also acid reflux....this has been ongoing for last 10 years. Gave up smoking 35 years ago. Worked in dental field, also in medical field. Had every childhood diseases known- born in England just after war...damp climate. Began with pancreatic issues five years ago and now after several tests I have been diagnosed with a mutant gene for Cystic Fibrosis. I don't have tCF just the gene.....perhaps this might explain some of my long term problems....always wondered why "mild" bronchiectasis caused such amounts of flem.

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Good morning....I am not managing the phlegm very well at the moment. I take a Zyrtec every p.m. to help control my sinus drainage as I have had major surgery and now have zero turbinates- so steady stream of fluid. I stay away from milk products and that does seem to help. For several years I was sleeping on incline related to reflex problems however as I aged it began to really put pressure on my lower back so we have removed the incline at the moment. I would be very happy for any suggestions. My usual plan is to arise two hours prior to any appointment and cough the majority of the phlegm up!!! Warm black coffee is a help!
Regards, J

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I submitted 2 sputum samples prior to starting the meds, I think I only got stuff from my throat. One was neg and the other was positive. I truly believe there is some of the MAC that lives in my throat. I had a little less of it about a month after starting the antibiotics but now it is hard to tell since I had some cold symptoms recently. I will wait to see once that clears up if I have less than prior to the meds.

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Hi @kiemen, I also had to do sputums and had none in my chest. I think MAC is in our throat/mouth becauce that is where mine was from and it was positive for MAC. They have so much to learn about these bugs.

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@jensfcv...After what I assume was sinus surgery, are you allowed to use nasal lavage with saline? I find that it cuts down on nasal mucus.
You might want to try an acid reduction diet to see if that helps.

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@heathert

Hi @kiemen, I also had to do sputums and had none in my chest. I think MAC is in our throat/mouth becauce that is where mine was from and it was positive for MAC. They have so much to learn about these bugs.

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I saw my MD and asked him about the Nitric Oxide. He said, he thought the treatment would be very expensive. I will be interested to see how this continues to progress.

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@egayle187

@jensfcv...After what I assume was sinus surgery, are you allowed to use nasal lavage with saline? I find that it cuts down on nasal mucus.
You might want to try an acid reduction diet to see if that helps.

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Thank you I am starting with nasal lavage again especially as we are in the pine pollen season. Have been doing bland food for a while since I have pancreas issues.

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@jensfcv

New to group....I have been diagnosed with mild bronchiectasis-also acid reflux....this has been ongoing for last 10 years. Gave up smoking 35 years ago. Worked in dental field, also in medical field. Had every childhood diseases known- born in England just after war...damp climate. Began with pancreatic issues five years ago and now after several tests I have been diagnosed with a mutant gene for Cystic Fibrosis. I don't have tCF just the gene.....perhaps this might explain some of my long term problems....always wondered why "mild" bronchiectasis caused such amounts of flem.

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As I mentioned below, there's certain foods causing your phlegm...start by noting what you ate the night before a particularly bad attack and go from there.
As for the bed, only an adjustable will give you the relief without the backache.

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@jensfcv

New to group....I have been diagnosed with mild bronchiectasis-also acid reflux....this has been ongoing for last 10 years. Gave up smoking 35 years ago. Worked in dental field, also in medical field. Had every childhood diseases known- born in England just after war...damp climate. Began with pancreatic issues five years ago and now after several tests I have been diagnosed with a mutant gene for Cystic Fibrosis. I don't have tCF just the gene.....perhaps this might explain some of my long term problems....always wondered why "mild" bronchiectasis caused such amounts of flem.

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@jensfcv - Welcome to the group! I have Bronchiectasis, MAC and atypical CF. I don't have the gene but I tested positive on multiple sweat tests. I have another one coming up in April so we will see what happens with that. I do breathing treatments with 7% hyper saline every morning and evening beginning with a couple of puffs of Albuterol to open the airways, the saline treatment to thin the mucous, then the Aerobika to pull it up and out. It takes about 30-40 minutes. It works pretty good. If I have a runny nose in the morning, I take a Sudafed to try and cut down on the drainage. I rarely battle with phlegm during the day; however, there are some nights when I go to bed that I'm coughing up more that came out of nowhere. Probably caused by something I ate but I haven't put much thought into what causes what. I just eat what I want. I notice that when I do yoga and lay down on the mat, I cough up phlegm even when I do my breathing treatment before I go. It's pretty embarrassing because everyone is all "zenned" out and I'm coughing my brains out. I usually have to tip toe out and go to the ladies room to cough up my stuff. I'm not sure if the Bronchiectasis is causing most of the phlegm or the CF. It's a mystery... Linda

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