Discussions

I have had Bronchiectasis for about 2 years. I started a prescription of Lexofloxacin for 7 days.

After three days feeling much better I quit coughing up mucous. My question is WHY?

I am happy about it, but I can't keep taking an antibiotic to feel good. I am on a 10 day vacation and didn't want to be sick the whole time.

All insight appreciated.

Thanks john

The COPD Foundation is excited to announce that we are hosting a discussion with Dr. Addrizzo-Harris, a pulmonologist and professor of medicine at NYU Langone Health, and Dariel, an NTM lung disease patient, to talk about living with NTM. Be sure to tune in to the COPD Foundation’s Facebook page on Thursday, February 28th at 1pm ET. This event is sponsored by Insmed Inc.

I think the drug called INS1007 to treat Bronchiectasis not linked to Cystic fibrosis,

Love to know anyone heard or is participating in the test?

Newbie here. Diagnosed last month with Bronchiectasis and severe Obstructive Sleep Apnea. I want to learn and I think many of you have already walked where I’m likely headed. First night last night on my CPAP machine. My Bronchiectasis not riled up right now but that could quickly change. I’d like to know how anyone coughing uncontrollably for a month or a few months due to Bronchiectasis can possibly wear a CPAP machine at night?

Eventually I’ll ask my pulmonologist’s advice on this. But the Pulmonologist told me a couple weeks ago that during my sleep study 148x per hour my airways closed or partially closed. He’s concerned my lungs are small....(note: didn’t know lungs came in small, medium and large). So, when I do see him next, he is not going to recommend I discontinue the CPAP, I’m quite sure.

Any of you have both of these conditions? What are you doing about your daily CPAP when the nonstop bad coughing comes to visit?

Hi - after treating MAI for a year with the big 3 (azithromycin, rifampin, ethambutol) with no improvement, we essentially doubled the dosage + used Amikacin via nebulizer (after a visit to National Jewish Health). Over a year later, the MAI was gone - hooray - and I went off the meds. Then, last year, I contracted pneumonia twice and, in December, the MAI reappeared. I'm back on the big 3 (not yet Amikacin) and will continue for a year. HOWEVER, at this point, I'm looking at alternatives (in addition to healthy eating, exercise, etc.). Any suggestions? People have recommended: vitamin D supplements, Bacteril, even colloidal silver! I would really welcome opinions as to whether any alternative approaches are useful. Thanks so much?

Hi, I am very newly diagnosed with Bronchiectatis, Mycobacterium Abscessus, and Aspergillus. I am feeling a little overwhelmed to say the least. I will be going to National Jewish Hospital in Denver for a second opinion sometime in the near future. My infectious disease dr has started me on Voriconazole. And I had a question about it. Has anyone had a negative reaction to this after taking it for several weeks? I am mainly experiencing nausea that will not go away I could also use some encouraging words. This is not the way I planned to start 2019!

My first culture results came back from December bronchoscopy. M. Fortuitum is growing. It is one of the so-called "fast growing" NTMs. Anyone else diagnosed with this one? Were you treated for it? I'm searching my references and don't find much specifically on treatment, except it is mentioned in this video from Dr. Huitt at National Jewish Health. https://youtu.be/Dw8hVJp1sJU

I'm 2 weeks out from a bronchoscopy and I know I have more weeks to wait until the NTM culture is done/read, but I think aspergillus doesn't take that long. I was thinking the last time I had it done it was about 2-3 weeks. Does anybody know? Thanks!

Hi, everyone --

Just joined today!

I've read this thread HTTPS://WWW.BRONCHIECTASISANDNTMINITIATIVE.ORG/BRO...

and would love to know how things are going with Kim. I would also love any input that members can offer for my situation.

My lung cancer is subsequent to my NTM (MAC). I've never been treated for the NTM, and don't yet know what treatment will be proposed for the cancer.

Here's what I distributed today to an NTM support group that I joined last year after attending a New York University (NYU) patient education program.

=============================

I have significant NTM infection/damage, and have just been diagnosed with squamous cell carcinoma in a small lung mass, plus metastatic SCC in same-side hilar lymph nodes. It has not been staged yet.

David Kamelhar is my NYU pulmonologist, and Gaetane Michaud did the NYU bronchoscopy/biopsies.

I have an oncology team at Memorial Sloan Kettering (from a 2016 anal cancer), who will be comparing the current pathology slides with those from 2016 to determine whether the new tumor is primary or metastatic.

Has anyone else dealt with a lung tumor and NTM simultaneously? At NYU and/or MSK?

Thanks for any input!

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Katie Keating (KSmiles123) responded by referring me to this 360 site.

I'd be grateful for any relevant input.

Happy New Year to everyone!

I just learned I have sleep apnea and am being fitted with a CPAP. What do I need to know about using CPAP as it relates to my MAC and bronchiectasis?

It seems like disinfecting may be a problem. I don't think CPAP mask, tubing, etc can be boiled like my nebulizer and Aerobika. How do bronchiectasis patients sterilize their CPAP?

The CPAP has a humidifier which creates a mist. Will I have to buy Sterile Water from a Medical Supply so I don't introduce more bacteria into my lungs?

Thanks, Dana

I'm supposed to fly from SC to Denver on 12/20 for a week.

My ritual is to go to bed around 10PM. As soon as I lay down I cough up phlem for a few minutes and then I can sleep for a while-usually.

Then up at 7 and do my inhalers

Then yogurt and coffee.

At noon after lunch, I lay down and cough up more phlem and then sleep for an hour or two.

Then I get up and have a beer around 3. At 4 I have a bourbon and then one more.

I feel a little better-but not much.

I'm really worried about going to Denver in this condition!

Is this the best I can hope for??

I nebulize 3% saline and use the Aerobika and huff cough twice a day. (I have also tried the Acapella.) I ride a stationary bike and walk on a treadmill for aerobic exercise. Even with all of this I’m not very successful with mucus clearing. My pulmonologist prescribed an AffloVest. If you use one, how do you like it? Thanks, Dana

The main idea behind controlling your breathing with Buteyko is that many people over-breath. I have found some success with this for Bronchiectasis. It take lots of practice, but it seems harmless and it's free.

We are seeking quotes to inspire and gather encouragement when life gets us down. Living with a chronic illness can bring dark days and loss of hope. Is there a saying or a famous quote, a pearl of wisdom that brings some positive light to your life when you feel that you are at the end of your rope?

Hello, I am looking for different treatment options for my mother who has Bronchietasis. I was wondering if anyone has tried cannabis (cbd oil, edibles, etc.) for their Bronchietasis? Obviously I feel like smoking cannabis would be counter productive but I was wondering if anyone had positive experiences with cbd oil for pain management, etc.? Thank you in advance

I have Bronchiectasis and I am supposed to go to Denver for Christmas. I have not traveled on a plane since I came down with this. I'm wondering if going to Denver for a week is such a good idea. I cough a lot and after my inhalers I cough up Phlem.

Thoughts?

Thanks sut

Hello everyone I am Kandy from South Dakota. Been sick most my life asthmatic overlapping copd, chronic bronchitis every year. Found I had bronchiectasis in 2014. Many end of life predictions starting at 10 yrs old. 1997 very sick told to get my affairs in order came home on oxygen. Been in hospital 2006 for strep pneumonia, 2015 exacerbation and this last Sept exacerbation they done a bronchcoscopy first for me. I just fight on as best I can.

I been advocating since 2009 beings many family members been asthmatic putting info in our papers and around the area. In 2013 some one told me to get hold of the Copd Foundation so I did. I received my title of Captain of South Dakota for advocacy in 2013. In October I write to our Governor and get the Proclamation making South Dakota Copd Awareness Month. Every year I have a copd event in my town. Write articles for papers in the area. As of now we have 3 captains for SD. I will have an event on Nov 3rd with our hospital bazaar. Also have a demo on our local radio station for November.. I put articles in the stores and at our local clinic. This year my daughters are helping me beings my health hasn't been good.I am admin in several support groups on FB and belong to several. Also 360social member.Wish me luck at the event!! I have been going to pulmonary rehab since 2012. Its 3 times a week not easy but I am there doing what helps me.

Do you have any item, like a de-humidifier, etc. that has a positive impact on your quality of life while dealing with a respiratory disease? Any recommendations?

Is there anyone here that got NTM after having chemo/radiation for lung cancer?

I am trying to make sense of what NTM is, why the treatment makes me so tired and what I can do to get past the tiredness.

Any advice?

Good or bad. Give experience traveling with medical equipment. Nebulizer, VEST system, clearance system.....

I read that calcium channel blockers can cause silent GERD symptoms such as coughing and that this is correlated with respiratory diseases such as bronchiectasis (BE). My dad has been on calcium channel blockers and has had a severe cough and now diagnosed with BE.

Anyone experiencing nail bed problems and losing fingernails.

My experience is I started getting artificial nails in October or December of 2017. I've always had beautiful nails, but I got gel nails and the last lady that removed them, damaged my nails. I started hitting my fingers or nails, not on purpose, just weird to explain. I had been complaining many many months before about my toenails looking green. Doctors kept saying just a toe fungus. Of course I say it's related to having pseudomonas.

In April 2018, again I hit my finger and fingernail very hard, I thought I broke it, but it was a sprain. Nail broken underneath, nail bed. Continued to keep it bandaged for months. Then it and another 'hit' nail completely came off.

I finally saw a dermatologist a few weeks ago. First, she said I have clubbing, which me and my pulmonary doctor disagree on. I presently have one full nail about to completely fall off and two nails that are black....fungus.

In 2017, bouts of pneumonia caused by pseudomonas. The meds I was given twice levofloxin. It C A N nail bed and fingernail issues and so can bronchietasis.

Just wondering are you having the same experience. What was done? The dermatologist original sent two prescriptions to a online pharmacy she uses. 1 was $240 and the other over $2000....yes, no mistake $2000. My insurance refused that. I hope to hear people experiencing the same.

My immunologist discovered through blood tests that I have very low levels of CD8 killer T-cells. He says in about a decade they may be able to correct this genetic defect. This may be a piece of the puzzle why I have bronchiectasis and a history of pulmonary NTM. This also explains why I am so susceptible to yeast/fungal infections especially when on antibiotics.

Medicare switched me to Lincare as my service provider for nebulizer equipment. When a new compressor and cups were delivered I was given directions for use. The provider told me that Lincare believes that washing the nebulizer cups with soap is to be avoided because bubles can form and interrupt the flow. The care provider showed me how to simply rinse all equipment ( except hose of course) under a faucet with my hands in warm water. I had always been washing the pieces with soap and water and then rinsing them after each use and actually boiling the pieces for 10 minutes once a week. . What do others do?

After being off treatment for MAC with bronchiectasis for 3 months my sputum cultures are positive once again. My doc is referring me to National Jewish in Denver for assessment and treatment plan. If you've been can you share your experience so I'll know what to expect. Thank you