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.
Kathy, I have that same wedge between my mattress and box springs tapering from 5" to 1", it works fine for me. The wedges that only go to your waist can potentially make things worse by putting a kink in your GI tract, not to mention possibly being hard on your back. I also try not to eat anything 2-3 hrs before bedtime.
Oh my gosh....it is uncanny. Dealing with handling a diet can be challenging too. Makes travelling a worry at times. Thanks for sharing. Have wonderful holidays.
Poodledoc, I found the same thing with a wedge when I tried one and, actually, it ended up in the floor most nights. I find that it also makes a difference what I eat and drink (as well as the volume) even 2-3 hours before I go to bed.
Thanks Irene! Your vitamin D comment made me start taking my vitamins again.
I agree. I had the half wedge and it was very uncomfortable! I was beginning to have a constant pain in my hip from sleepy on my side. The full I e is so comfortable I wonder if it’s actually working.
migizii, please read through each of these links to see if K2MK4 is a stone unturned that may offer relief for your bronchiectasis. Notice at the end of the westonprice link the stress is on food sources mentioned not supplements. That is where your money is best spent.
https://www.westonaprice.org/health-topics/in-defense-of-vitamin-k2-mk-4-dr-prices-activator-x/
https://www.sciencedirect.com/science/article/pii/S0306987716309884
About sleeping on wedges: Dr Huitt urged me for years to get an adjustable bed. She didn’t like wedges because, she said, you slide down as you sleep, reducing the benefits. With an adjustable bed, you also raise your knees, keeping you from sliding down. I finally bit the bullet, got rid of the wedge and, wow. So much better. The next time I saw Dr Huitt, I told her I finally listened to her advice.
I find the conclusions of the Science Direct article very compelling. I am already a taking Vitamin K2-MK4 supplement.
I take 81 mg of ASA every day and read that K2 can affect coagulation. I thought I’d ask the hematologist when I see him in December but wonder if anyone has any experience with this?
Thanks in advance.
K IS a blood thinner. When I finally stopped taking it, the phlebotomist no longer blew my veins.