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BronchandNTM360social welcomes new member Corrine T who
joins 5,535 current members of our community.
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Hey there! We have a CCN Center in San Diego. I will link the site details page so you can see a list of the providers. UC San Diego.
Does anybody have a pulmonologist in San Diego who they have found to be an expert in bronchiectasis?
Brandon,
Thank you so much for the reminders. It is okay to occasionally have other than a balanced diet when you are exhausted, overwhelmed with medical appointments, therapies. Having support enables us to keep moving forward. We understand your challenges and are here for you.

💙 Mental Health Month 💙
Living with bronchiectasis or NTM can be exhausting in ways people don’t always see. The lack of sleep, stress, fatigue, worry, treatments, appointments, and constant balancing act can wear on both the body and the mind. 🌧️
And sometimes, when we’ve been pushing through for too long, we forget that our mental health deserves care too.
Here’s the honest part: sometimes we’re all running a little low on fumes. 😮💨
And here’s the important part: asking for help is not giving up. It’s actually one of the strongest things we can do. 💪💙
Sometimes help looks like:
🫶 Talking with a friend
📞 Reaching out for support
🩺 Speaking honestly with your doctor
😴 Giving yourself permission to rest
😊 Or simply admitting, “I’m overwhelmed right now.”
And sometimes it’s realizing that stress-eating cookies for dinner may not count as a complete wellness plan. 🍪😄
Please be gentle with yourselves and with each other. This community was built for support, understanding, encouragement, and yes… a few smiles along the way too. 🌿
You are not alone. 💙
Change, adaptation to a new site does take a little time but we believe that we will be a more connected community as time goes forward. We are so happy that you have found us and we hope that you will check in regularly. 😍

The new Bronchiectasis and NTM 360social experience is here — and we’re so excited to finally welcome you in! 💙
For more than a year, a tremendous amount of work, collaboration, thought, and heart has gone into building this new space for our community. Every update, feature, and improvement was created with one goal in mind: making it easier for patients, caregivers, family members, advocates, and healthcare partners to connect, learn, and support one another.
We wanted this space to feel more welcoming, easier to navigate, and better connected to the resources that matter most to our community. From educational materials and conversations to Care Center Networks and shared experiences, we hope this new platform helps make finding support and information simpler and more meaningful than ever before.
Most importantly, this community continues to be built around the patient voice. That has always been at the heart of Bronchiectasis and NTM 360social — and always will be.
We know change can take a little getting used to, and we truly appreciate your patience, feedback, and encouragement as everyone settles in and explores the new features and layout. Your conversations, kindness, experiences, and support are what bring this community to life each day.
Thank you for growing with us and helping make this such a special place for so many. We can’t wait to see the new friendships, conversations, learning opportunities, and moments of encouragement that will continue to grow here together. 🌿
Many Thanks for the information,best wishes Eileen.

Looking forward to this year's celebration! So many wonderful plans are being put into place for our global community.
Hello! Early heat waves are occurring in parts of the USA today. Do you understand the meaning of the dew point, heat index and how it can impact individuals with respiratory issues? The blog article below defines such terms used by meteorologists that may assist you in better understanding the weather forecast. Many people listen to the temperature only and do not pay attention to the dew point number. Being prepared for changing weather patterns will assist you in planning throughout the summer months. Why Weather can Worsen your Lung Condition
I am looking forward to the 5th annual World Bronchiectasis Day! We have come along way in the Bronchiectasis space over the past decade. World Bronchiectasis Day continues to increase public awareness, education on the subject and research opportunities. I hope that you will assist in spreading the word about World Bronchiectasis Day!

Mark your calendars! On July 1, World Bronchiectasis Day brings us together to raise awareness about bronchiectasis around the world 💙
This year, the Bronchiectasis and NTM Association is partnering with nearly 30 global organizations. Bronchiectasis rates are rising worldwide, but this chronic lung disease is still under-recognized and under-diagnosed. Together, we can help more people get a timely diagnosis, access high-quality care, and live well with bronchiectasis.
Stay tuned for upcoming events, posts, and activities in honor of World Bronchiectasis Day 2026. RSVP now to join on Facebook: https://www.facebook.com/share/1D21fKNfpQ/
Learn more at www.worldbronchiectasisday.org
Janh,
I fully understand. We do find out who our true friends, support system is over time. I got tired of explaining my situation to others and continued to socialize with only those who listened to me and understood that I was dealing with a chronic condition . These people understood that I was not contagious. We cannot fully social isolate ourselves since that can add on to our current challenges. Social isolation can lead to greater angst.
Janh,
I am glad that coughing is a little less. Hopefully, you will experience more relief soon.
Yes, vitamin A and other vitamins can be the cause of dry skin. Eucerin or other good quality skin lotions can lessen the dryness.
Maybe have blood work drawn for vitamin and mineral deficiencies. Medications can sometimes causes deficiencies in these areas. With that said, deficiencies in some of these areas can cause dry skin.
This is great new information!!
I definitely think as a women it very much affects my social life. If I talk I get coughing and mucus. People stare and ask are you sick. I don’t like to discuss either everyone. So I find myself missing a lot. Miss cards going to lunch talking with people.
I have been on it for 4 months I have dry skin and have one reapirtory flareup. I agree mucus production not affected. Coughing a little less.
A little information on reverse osmosis for those who are unfamiliar with this method:
- Studies indicate that properly functioning reverse osmosis systems can significantly reduce or eliminate NTM from water.
- The effectiveness can depend on the specific system design and maintenance.
- Regular maintenance and monitoring are crucial to ensure the system operates effectively and continues to remove contaminants.
Many thanks for the information,regards Eileen
Reverse Osmosis is how we filter our water,hope this helps
Dry skin is treatable. Do you take a daily vitamin in case one of your vitamins maybe low as well?
I realize that this update in boiling water may have some individuals questioning whether or not 3 minutes is adequate time to boil water after being accustomed to boiling water for 10-15 minutes.
I have been boiling water for over 10 minutes for many years. This latest research on boiling water was done at 10 centers throughout the country.
I am adding 2 extra minutes for extra precautions, my personal preference. Five minutes is still far better than 10-15 minutes.
I am noticing one side effect....... dry skin. I began using OTC healing lotion which helps with that one.
Hello! Springtime can bring on an increase in respiratory symptoms for some individuals. Many respiratory symptoms overlap in different respiratory disorders. Do you understand what causes wheezing? The blog article below reviews the causes of wheezing and treatment options.
Wheezing and the Bronchiectasis/NTM Patient
Please let us know if you have any questions.
Kalli,
Thsnk you for posting this great podcast on health equity. Everyone who has a diagnosis of Bronchiectasis and NTM deserves to be treated fairly regardless of their zip code. The expansion of the BNTM Care Center Network's intention is to provide greater access to patients throughout the country. There is hope that more virtual visits will be possible in the future.
Hello! I have great news to report on the time required to boil water to get rid of NTM. Jennifer Honda, PhD ,BNTM water expert presented an update at the recent NTMir Patent Conference. The research study, referred to as the BANTER study, Boiling Assessment of NTM in Tap Water Evaluation Regional, included top BNTM experts throughout the country including Dr. Joseph Falkinham , National Jewish Health and 7 other BNTM experts. The new recommendation is to boil water for 3 minutes!!! Wow! What a time saver. We don’t have to be concerned about boiling water for 10-15 minutes anymore when we are at home and or out and about. I look forward to hearing more positive updates that will lessen the time we need for daily therapies.

Happy Friday! Have you listened to the latest episode of the Bronchiectasis and NTM Association Podcast?
This month's episode explores the important topic of health equity. What is health equity, and how might it impact your bronchiectasis diagnosis and treatment? Hear from Dr. Shoshana Zha, Care Center Network (CCN) Center Director at the University of California-San Francisco, and Dr. Rocio Hurtado, CCN Center Director at Massachusetts General Hospital, who discuss how where you live, income, race, language, and insurance can affect diagnosis, access to specialists, and timely treatment for those with chronic lung disease.
They also highlight current projects and long‑term goals of the CCN’s Health Equity and Access Working Group.
Give it a listen wherever you get your podcasts: https://copdf.co/Bronch-NTM-Podcast
Ellen,
You are most welcome! I fully understand the GI challenges- I have been there. GI issues can be very complicated- mixed views on how to treat. I am here to assist you on this part of the journey.
Roberta,
Hello! Thank you for sharing your experience with our community. I am sorry that you had adverse reactions to Brinsupri.
Working on it - just started seeing a new GI doc. Thanks for your input.
I started talking it & developed headaches shortly after starting. I also had severe GI issues. Had anyone had this?
Please keep us posted Tim and good luck
Tim,
Hello! You are most welcome! I hope that you do see more results in time. I assume that you have discussed this with your Pulmonologist who has prescribed Brinsupri?
Thanks for your reply. I've been on it for about 10 weeks now. Not sure what to expect in terms of results other than the claim that it will reduce flare ups. I've noticed no side effects as yet, so that is good. However, I cannot say it has reduced my daily symptoms (mucus, coughing, etc.) at all. I am hoping someone else may be on it as well so I can hear their experience with Brinsupri.
Tim,
Below are the most frequently asked questions on Brinsupri: https://www.brinsupri.com/frequently-asked-questions/
Tim,
Hello! I haven’t taken Brinsupri yet but I have heard a lot of positive results recently. Brinsupri takes an average of 6 weeks or more to show results.
I started taking the newly approved BE medicine Brensupri in February of 2026. I'm interested in any feedback from others who are also using this medicine.
Thank you
Brandon,
Hello! Adorable dogs, :). Wishing you a day full of smiles and peace as well.
Hello! I hope that you are having a good day as well. :)


☀️ Good morning, BronchandNTM360social! ☀️
Just wanted to check in and wish everyone a really good day today. 💙 Whether you’re tackling treatments, trying to pace yourself, enjoying a little fresh air, or simply making it through the day one step at a time, we’re glad you’re here.
How’s everybody doing today? Any wins, questions, good news, favorite photos, or even just a quick hello to share with the community?
Wishing you plenty of deep breaths, small smiles, and hopefully a peaceful day ahead. 💨🌼
Ellen,
You are most welcome! Being on a lo Fodmap diet can be challenging on a long term basis. I hope that you have a great GI/ Integrative Health Care Provider or Registered Dietitian to assist you.
Kalli, Thank you for this great post. It is great to read about the research done about the differences in the outcomes of lung diagnoses in women and men. I look forward to reading updates as more research unfolds.

Did you know that bronchiectasis can have a more significant impact on women than men?
Studies show that women:
🚺 may be more likely to develop bronchiectasis
🚺 are more likely to develop bronchiectasis at an earlier age
🚺 experience greater social and emotional impacts from the disease
In honor of National Women’s Health Week (May 10-16), read the latest research on sex-based disparities in health care experiences for chronic lung disease. Check out the article in Chronic Obstructive Pulmonary Diseases: Journal of the COPD Foundation from our friends at the COPD Foundation.
Read the article here: https://copdf.co/perceived-differences
Hello! Many respiratory symptoms overlap. How is bronchiectasis like asthma? Bronchiectasis inflammation is usually the result of a lung infection. Your immune system responds to infections. They release chemicals that cause airway inflammation. When this happens, it can damage the tissues lining the airways and eventually lead to airway scarring.
This scarring causes airways to become abnormally dilated. This causes mucus secreted by airway cells to become thick and sticky. The accumulation of thick, sticky mucus in the airways creates a breeding ground for germs to collect. This is why people with bronchiectasis are prone to repeated lung infections.
Bronchiectasis and asthma are both associated with an immune response. They both can cause flare-ups. Common symptoms of both are shortness of breath and coughing. Asthmatic airways are hypersensitive. This makes them “spasm” when you’re exposed to your asthma triggers. It also caused increased mucus production. This is what causes shortness of breath and coughing due to asthma. These flare-up episodes are both treated and controlled with asthma medicine.
Repeated respiratory infections worsen airway inflammation. Mucus can become thick and obstruct the airways. This is what triggers bronchiectasis flare-ups. This is what causes shortness of breath and coughing due to bronchiectasis. These episodes will not respond to asthma medicine. Treatment usually entails antibiotics and other treatments.
Unlike asthma, bronchiectasis sputum tends to be colorful. It may be yellow, green, or even bloody. Bronchiectasis may also present with fatigue, fever, chills, weight loss, and night sweats. Do you have both asthma and bronchiectasis? Let us know if you have any questions.
Hi - thank you for your feedback. I've been eating low Fodmap for a couple of years. I'll let you know what the SIBO results are. Appreciate the feedback.
Hi Val A. Welcome to the community. Check ins are meant for quick status updates such as saying hi or letting everybody know how you're doing. Some of us share photos of pets or other fun things. As more posts are added to the activity feed they move further down off of page 1, so they are not as visible to the community.
Discussions are for more in depth discussions and will remain visible to the community much longer. Every time someone adds a reply it will display in the feed, no matter when the discussion was added, so it can be visible on the feed many times adding more visibility to the discussion.
The comment about sharing personal medical info is just reminding you it's a public community, so for security and privacy it's best not to share names and addresses and things like that.
Hello - I was happy to hear about this site from a newsletter. I was going to do so. However, I'm confused about the note I see below that reads, "Please do not share private medical information in your check-in text or photos." Are these types of disclosures meant for the discussions section?
It is not our intention to serve as a substitute for medical advice and any content posted should not be used for medical advice, diagnosis or treatment. We make every effort to support our members, our medical professionals cannot and will not provide a diagnosis or suggest a specific medication; those decisions should be left to your personal medical team. While we encourage individuals to share their personal experiences with COPD, please consult a physician before making changes to your own COPD management plan.
Community posts are monitored by the 360social Community Manager, as well as staff respiratory therapists, educators, and other medical professionals.