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Long-term Antibiotics for Bronchiectasis & MAC

MAC & Bronchiectasis | Last Active: Aug 14, 2020 | Replies (164)

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@jkiemen

Which antibiotics are they? Have your CT's been stable?

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Replies to "Which antibiotics are they? Have your CT's been stable?"

Macjane....what you have shared makes me so furious.....my heart goes out to you....I hope you are getting the care you need and are entitled to. Tdrell

Mac jane I was told by NJH that I needed to get bed whose head elevates to 30 degrees and also sl at knees. I they tell me that I have had MAC and various other weird bacterium in sputum/lungs as a result of my Gerd.....that the bacterium gets into lung then sputum when I silently aspirate stomach contents which contain the weird bacterium into lungs. Not supposed to sleep on right side or stomach. Have to follow their Gerd diet....page long.
I tried looking for beds a year ago and got really confused......all the options! Would love to hear what others say.tdrell

I had the same reflux advice. I changed my diet,and got rid of the reflux. I sleep on two stacked pillows. I knew I'd get no rest half sitting up. It worked for me.

I bought a 7” wedge at Bed, Bath & Beyond. I use that and my regular pillow. I’ve read others just put blocks under the legs at the head of their bed to raise it up. I would prefer to do that put I have a 4 poster bed and it wouldn’t work.

@macjane I sleep with 3 pillows and on oxygen at night only.

@macjane I ride my bike often. It was difficult at first, back in 2014. I am conditioned to it now and in better shape. I don't have to stop to catch my breath when riding any longer. My hubby and I walk every evening around a big block (30 mins). I avoid swimming pools because I do not want to chance catching mac again. Exercise is the best thing we can do for ourselves.

@macjane, it is funny you should say that about diagnosing Sarcoidosis. In my cousin's case, I suggested she may have sarcoids 8 months prior to three doctors she had seen who couldn't figure it out. She finally went to a specialist at UCLA and had it diagnosed. I guessed that is what it was because I had been on auto--immune sites for years trying to figure out my own illness. Many of her symptoms matched with what I had read.