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7% Saline Success Story that warmed my heart.

MAC & Bronchiectasis | Last Active: Apr 23 9:51am | Replies (79)

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@kathleenlp

Yes, I agree that this forum has been so informative and helpful!! I'm so grateful to Sue and others! I have Bronchiectasis, Mac abscessus and possibly Aspergillus(positive tested but been treated).
The Saline was a huge game changer for me! I am religious about using it twice a day along with bronchodilator and steroid inhaler. Even when I travel!! In the past 3 years my CT has improved greatly with some areas completely "resolved" My PFT has also improved each time. My immune system is much better too. I am very active and also try to keep informed and try new things. I also have been on NAC forever.....even before diagnosis plus an array of "whole food" supplements.(Agree with Sue, be cautious and do your homework on supplements.) Glutathione, but only sublingually, and a product I love...Biocidin....you just have to read up on that. Also sublingual. Airway clearance twice a day. Exercise daily!! At least 30 minutes....just added a rebounder to my regiment and I love it. This clears lymph system and really gets your heart rate up. It's sometimes a struggle to juggle it all. My husband has Alzheimer's and Lewybody and I am his caregiver too. I want to stay healthy to care for him. Dodging respiratory illnesses is the challenge! Especially this time a year. We are a target for that. I say don't give up or become despondent... try to fight.......everyone is different and you might have to experiment but can hopefully you can improve your quality of life! Blessings in the new year!

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Replies to "Yes, I agree that this forum has been so informative and helpful!! I'm so grateful to..."

Thank you kathleenlp for your encouraging post. I do hate doing the saline 7% - thanks for the 'push'.
You have much on your plate. All the best to you in your health and in your caregiving.

Due to just beginning to comprehend much of what is good to do with BE I decided to read again the posts where you and Sue mentioned Glutathione. I have a slight, per October sputums at NJH, showing of Macobacterium avium intracellulare. NJH indicated they did not want to start anti biotics because3 sputum viles showed so little infection. Hope that was the right decision...we shall see. My PFT all good results. To me my main problem at this point, is the slight MAC and the moderate showing on the C Scans. The only thing NJH suggested and started me with is the Vest, Aerobika, and 7% for nebulizing. I have started taking liquid guaifenesin and going to look into the NAC. I also take several supplements including D, Zinc, C, Garlic, Tumeric, Fennel etc. etc. Have you had any experience with Mullein or thoughts about it ? Is the Glutathione taken due to Bronchiectasis or another type of problem? What would that be prescribed for?