Airway clearance and how I feel throughout the day
Hi everyone,
I know it might be a diffuse question, but let me try.
My pulmonologist told me if I do the airway clearance correctly. I
should feel clear of mucus during the day. I spend almost 30 minutes
doing it (flutter + autogenic drainage in the morning and evening). But throughout the day, I have to constantly clear out mucus most days. I am wondering what your experience is, is it normal for you? Maybe I am too sensitive about it.
Your experience is greatly appreciated.
Many thanks!
Ling
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
Wow, this is a good map. OHSU is where my pulmonologist works. ALan Baker, the specialist in bronchiectasis, is not seeing patients any more. I have tried to see him in the past. But I am going to see Dr. Winthrope in September. He is an ID doctor.
Thanks a million!
Ling
If I were at the beginning on my bronchiectasis journey @wangling I *might* consider a TCM or Ayurvedic consult...I know what you mean about poison in medicine. American medicine *tends* to treat symptoms not root cause in many cases.
I have heard from a number of people that they developed Bronchiectasis after a bout of pneumonia. In fact two people in my very town were diagnosed with mild Bronchiectasis after struggles with pneumonia. One of them said he just kept getting pneumonia or infections prior to finally seeing a pulmo who diagnosed the Bronchiectasis. So you have to wonder if the cart came before the horse or visa versa. In my case I had a very severe flu virus (chest cold) and the coughing up of mucus never stopped after that virus. I also had repeated chest colds prior to that. They do say that repeated pulmonary infection is one cause of Bronchiectasis. Perhaps my immune or D levels were low back then. If you only have little clear congestion you probably do not need saline. I have a great deal of congestion. But could the saline discourage MAC from developing? Or would the lack of mucus be enough to discourage one from contracting it? These would be good questions for your Dr. Or if anyone else reads this and has input on that please do so! I agree with your upbringing about medicines being partly poison! But sometimes it takes a thorn to remove a thorn.
oh you are lucky Ling to have that appt! Ask Dr Winthrope about the saline in your case. Bring all your questions to him when you go! Remember that prevention is very important with Bronchiectasis. So even though yours is mild you could take measures such as avoid crowds. Avoid anyone who is sick of course. Wear a mask during flu season when you are shopping etc. I kept going to large crowded indoor events every summer for years. Pretty much every time I would come home with a very bad chest cold. I have no doubt that contributed to my Bronchiectasis becoming worse and worse. Cycles of repeated infection/inflammation/worsening of it. I wish I had known better. You are very wise to be pro active now especially at 71! I was in my 40's when I developed Bronchiectasis so i could get away with more (but should not have).
Thank you so much Irenea8. I do feel very lucky that Dr. Winthrop agreed to talk to me. I will try to get most of my questions ready. I am also lucky that you and other people in this group shared your experiences about your dealings with the conditions, and I truly benefit from that. And thank you for always being there. Yes, definitely prevention is important. I still wear a mask when in doors, like shopping, going to concerts and seeing movies. Get as much exercise as I can, yesterday we hiked in Mt. Hood area, it is great being in nature.
Take care!
Ling
You are absolutely right. I am planning to consult a Chinese doctor when I visit China in August. Thanks for bringing it up.
Take care.
Ling
Ah, not sure how I missed this posting. These are great questions to ask Dr. Winthrop. Please feel free to let me know if you have other questions. These questions are general concerns to all of us. Many thanks, Irenea8.
Ling
most likely he will say the repeated infections led to the Bronchiectasis. Something must be going on with lowered immune function?
Irene, I totally agree with what you said, "It seems that the pulmo's who do not know a lot about Bronchiectasis end up prescribing just Albuterol or steroid inhalers. And not the saline." Even worse, without testing sputum some pulmonologists and primary care doctors seem more than willing to prescribe long-term use of wide-spectrum antibiotics "just in case" - neither of these is helpful to our long-term health.
That is the great thing about Connect - we get to coach those newly diagnosed on how to find the right doc to help maintain their health. I don't know what I would have done without the support of this group for the past 5 years!
Thank you for sharing your long-time experience and showing us that Bronchiectasis is a disease we can live with - and for a long time.
Sue
I totally agree that low immune function is the culprit. So building up a stronger immune system is crucial.
Thanks Irenea!
Ling