Bronchiectasis: New Diagnosis
New to your group. Non-smoker. Pneumonia x6 in 12 years, double pneumonia twice. Was diagnosed with chronic bronchitis and COPD for past 15 years, now pulmonologist based on x-rays and MRI has diagnosed no COPD, yes bronchiectasis. Take advair 250/50 twice a day. Past ten days I am increasingly gurgling, wheezing, some chest pain. I have recently moved to Florida which I like but am having long wait times to get into see a family care NP who can hopefully refer me to a pulmonologist. I walk 20-30 minutes a day. Any ideas how to manage this now. Am worried about getting pneumonia again. I went to one walk-in clinic at a reputable hospital. They literally did nothing except take x-rays. Didn't even talk to me. Just billed $2000+ for x-rays. Do I try another walk-in clinic. I feel very alone right now with this chronic medical problem.
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
@auntnanny I couldn't have said it better. I feel the same way.
I'm 5 weeks into NTM treatment with the "big 3" and everything was going well (body adjusting to the meds, increased energy, reduced cough, etc.) until yesterday - Friday - at 5 minutes after 5 pm. I felt a sudden need to cough and coughed up blood. I couldn't reach my doctors because it's the weekend and I knew I hadn't coughed up enough blood to warrant going to ER. The experience put me in a mild state of panic. I managed to calm myself down and the bleeding didn't continue but I want to understand it. Has anyone else coughed up blood while on the treatment? If so, what was the explanation?
@onana Hi there. I just now found this post of yours. I missed it last week somehow. As you have probably read from some of these posts, us mac patients sometimes do experience coughing up blood. It sometimes will happen and usually resolves itself. But, sometimes medication will actually cause it. In that case you would need to be taken off of that medication. Have you reported this to your doctor?
Thanks for getting back to me. Yes, I reported it to my pulmonologist and to the ID doc. The pulmonologist didn't think it was anything to be alarmed about (unless I was coughing up blood repeatedly. That wasn't the case. It resolved itself in one day. I got a message to the ID doc but didn't get to speak with him. I know the two docs talk to each other. They did not call off the meds.
@onana Good! I know that kind of thing can freak a person out; it did when it happened to me. How are you doing on the meds?
@windwalker I'm doing ok. The first couple of weeks I had stomach cramps and frequent trips to the potty (felt I couldn't leave the house for at least 4 hours after the dose). Now things are more comfortable. Seems my body has pretty much adjusted, although I still want a potty nearby after I take the meds. I feel more able to manage the side effects. Appetite is holding but diminished, so I try to eat high calorie but nutritious food. Phlegm is noticeably reduced, so the nebulizer saline doesn't bring up much at all but assures me that the meds are working. I was pretty excited about the good results until I coughed up blood. That incident really discouraged me, but I'm ok now.
I have been diagnosed with Bronchiectasis from my Pulmonologist. I had a couple Bronchoscopies done.
I wear a shaker vest 2 times a day. I also get an Asthma shot every four weeks. I also get I.V. treatments
for my Bronchiectasis every four weeks also. Been doing this for about two years now and still have a continued
cough with mucus. I feel like a lab rat when ever I go to the doctors office. Also have been on lots and lots of Antibiotics.
Is there any other thing I can try?
Hi @kpost2, welcome to Connect. You'll notice that I have moved your message to an existing discussion about bronchiectasis in the MAC & Bronchiectasis group. If you click VIEW & REPLY in the email notification, you can scroll back through the past and recent posts.
I also invite you to explore all the discussions in the group. There is a wealth of information here: https://connect.mayoclinic.org/group/mac-bronchiectasis/tab/discussions/
For example, this discussion:
- Long-term Antibiotics for Bronchiectasis & MAC https://connect.mayoclinic.org/discussion/bronchiectasis-mac-antibiotics/
- Are Nebulized saline and Aerobika beneficial? https://connect.mayoclinic.org/discussion/are-nebulized-saline-and-aerobika-beneficial/
One thing you'll quickly notice is that you're not alone. I'd like to introduce to a few members like @windwalker @tdrell @irene5 @kjellis and others who understand your feeling like a lab rat and searching for treatment/management options in support of or as an alternate to long-term antibiotics.
KPost, do you use a nebulizer?
@kpost2- Welcome to Mayo Connect. I'm sorry that you are having troubles with your cough and mucus build up. Are your IV's to fight infection?
I'm afraid that your symptoms are pretty usual for Bronchiectasis. Because you have permanent damage to your bronchi you will need to be very diligent about exposing your self to anyone who is ill. I don't know if this helps at all.
https://bronchiectasisnewstoday.com/bronchiectasis-treatment/
https://www.medicalnewstoday.com/articles/185768.php
https://www.nhsinform.scot/illnesses-and-conditions/lungs-and-airways/bronchiectasis
@windwalker @tdrell @irene5 @kjellis- Have you found anything new?
@kpost2
Welcome to the group.
I too am getting the nucala asthma shot...do you feel like the injection your getting is helping with reducing phlehm production?
I am also prescribed the Vest to help with phlehm that does help some.
Are you looking into allergies that would cause more phlehm like dairy dust mold in the house. Just a some things I have to be watchful of.
Hope you get some answers to reducing the phlegm production.
Shari