Celebrating an antibiotic-free year
And I’m convinced 7% nebulized saline did the trick. (Accompanied by percussion vest vibration) And this forum is the place I learned of “The 7% Solution.“ “Don the indebted.”
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
@macjane, I am puzzled. Why did you need to lay down and eat due to depression?
Hi Windwalker. Thanks so much for the article. I learned much from it. I have had this ring stretched twice now and the second time all the tests were done at Mayo, Rochester. At this point, they did not recommend any further intervention but I am to contact them if symptoms of problems with swallowing begin again.
In reply to alleycatkate....my pulmonologist was the doctor too who sent me to gastroenterology to check on GERD when he heard my symptoms.....great minds think alike! Hope you are doing well too.
In reply to gej53.....May I ask how much you pay for the solution on Amazon as Pt. D doesn’t cover this and so far, I haven’t had any luck with getting it covered. Your situation sounds so much like mine....do you have MAC? I initially had some very strange bacteria that my pulmonologist did not treat and no other “bugs” have shown up, although he rarely has me do a sputum test as my bronchiectasis is not progressing very much on yearly CAT scans.....my energy levels fluctuate and my weight isn’t that easy to hold on to (many people feel jealous, but not when one wants some weight). Otherwise, I’ve been pretty good king health wise. Twice daily nebulizing must really be key! This is a valuable site. Stay safe and may you have a nice day😊
Thanks Kate. I am so out of shape physically so long walks are hard. I fell last year and destroyed right hip. They needed to put in very unusual replacement. This meant too much pain reliever that took a year to come off. Have a Safe holiday season. I take Vitamin D but need to come off Klonopin.
Morning! I experienced unrelenting coughing. They tried treating me as if I were experiencing allergies. My medical doc ordered a cxr and sent me to a pulmonologist. He did a CT and felt strongly I had MAC from the presentation of the CT. I had a bronchoscopy and he did biopsies and washings and they all returned no growth so he is treating the bronchiectasis. I still worry about the MAC. The nebulizing with a vest it the only thing that helps me clear my lungs. When I asked about 7% he felt it would give me bronchospasm. I am going to ask him again in January. It was around $40 for 60 vials. I am alternating it with my 3% to make it last longer. Since I did well with it I hope it will give me a script for it. I guess this is a lengthy response for asking the price :). I also have lymphocytic colitis so am scared to death to think about taking the ATB necessary to treat MAC. So far my CT scan has been stable from the previous year. Guess a little tiring to neb but am thankful that so far it seems to keep my chest stable. I still cough but nothing compared to my initial presentation. Sorry so wordy. You have a great day too!!!
@macjane ...Wow, Jane. It sounds like a very difficult year. I hope things continue to improve and that you have a safe and happy holiday also.
Thanks
Yes, the vest is covered by Medicare.
Hi! Thanks for the information. Once again, I find myself having another medical condition in common with you-lymphocytic colitis....it’s seemingly uncanny how we have these similarities. Also, I have have not yet faced any infections requiring long term treatments, yet. I hope we can stay well😊. Have a nice evening!