7% Saline in Nebulizer for Mac
Could you all give me your opinion?
I have Mac..don’t know species yet.
I’m new at this but have seen many posts on here about how important it is to clear the mucus. Saline in nebulizer, flutter valve!
I requested that my pulmonary call in a script for the 7% saline to be used in a nebulizer! His response was “just use the flutter valve, the saline could make things worse.”
I have read in this support group that everyone uses the saline and also videos on UTUBE…..etc. I’m confused.
What is your opinion on this?
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
Only the CT gives the picture the pulmonary wants is my understanding...
Hi Lilianna! I purchased the one in the link above in my post. Visiting a facility that does it is not affordable! I do it everyday that I can. Usually standing front and back 5-10 min each side then sitting 5-10 minutes each side. You cannot have any clothing on. You can target the areas you like. I have been doing it about 7 or 8 years. 😎
Hello is the link the same as the videos link. The talk about two companies selling products such as a helmet. Is it a lamp?
Hi lilianna
The top link is a medical/doctor link that I follow ....he gained popularity in the pandemic guiding people to natural/scientific healing and immune boosting practices.
The bottom link is the company where I purchased my panel....I have the biomax 600
I would not get a helmet. You want your lungs getting the light and face etc. The helmet is just for hair growth which you will get from the panel.
Oh my gosh! I was unable to tolerate the antibiotic treatment due to my GERD. But I've been using the saline nebulizer and flutter valve for the past few months. But I didn't know that it could decrease the amount of bacteria. I thought it just provided an inhospitable environment for further infection.
How long were you at NJH?
Did you find them to be exceptional?
I was diagnosed 2 yrs ago
MAC & bronchiectasis - very damaged lungs.
I did the things an infectious disease dr. Suggested.
I am stable per CT scan.
healthy bone
i was not told about saline when i was diagnosed with bronchiectasis and MAC- such a shame- i found about it here and asked the pulmonologist who said i could use it. if your pulmonologist is against it, just ask your primary care- thats how my husband got it for sinus. it can be purchased online without prescription but it is pricy.
Diagnosed with MAC in 2021. I was at NJH first time I think was 4-5 days. Lots of testing. Then repeat some tests after 6 months Now I just go back yearly. It’s only One day of testing now at NJH. I’ll have blood work, CT & sputum sample taken and then review tests with Dr. they are very knowledgeable, friendly & it’s really nice to see experts in the field. I don’t have a local doctor with expertise of MAC. But together I work with my pulmonologist to get my 6 month CT scan and whatever NJH suggests my doctors are great locally to get any tests that NJH recommends
Infectious disease Dr nor Pulmonologists have ever said anything about saline. Pulmonologists did prescribe airway clearance vest that I have been using for the past 7 years. It helps my breathing but I am continually picking up bacteria. The mucus gets trapped and they put me to sleep, go in an wash my lungs out every few years. It helps sometimes.
What is "NJH"?