My pulmonologist changed my medication from the spiriva handihaler to a spiriva mist that's more like an inhaler. So far this has allowed me to do alot more that I could. Maybe it's because it's new to my lungs and opens them much more.
@A MyCOPDTeam Member Hi, I have 3 inhalers that are mist, Spiriva Respimat, Stiolto Respimat, and Striverdi Respimat...of course I can`t use them all.. I can use 2 of them, Spiriva Respimat I`ve been on for a year or better and it by far is the best, I use it twice a day... the other 2 I have also tried, 1 for a month or 2 then the other for a month or 2.. The Stiolto Respimat seems to work best for me. I use it once a day(and sometimes twice in a day)
@A MyCOPDTeam Member I have "Obamacare". It is an HMO which I have to work hard at finding someone that takes HMO. I signed up for a $500 deductable, which I had to pay before my insurance kicked in on anything. Well I had that paid by getting my spiriva and symbicort back in January. So anything I get now I don't have to pay for. If I have to get xrays or other services I have to pay 20%. The pulmonologist has ordered chest xrays so I had to find a place that would take my insurance and fortunately it will only cost me $9.57. The pulmonologist gave me a 30 day sample of the Spiriia Respimat. But when I get my other medications I have not had to pay for anything. My Symbicort, which I picked up today, would have cost me $337.50 if I didn't have my deductable paid. I'm in Texas so I'm on Blue Cross Blue Shield TX, through Obamacare. Hope this has helped.
yes mine did also I like it seems to be working better
I use Spiriva Respimat, I a lso find it works better than the capsule
The instructions are to take 2 puffs per day. There are warnings on Google searches that there is a very small risk of it causing cardiovascular side effects.
However at 71 being able to breath more easily is far more important to me.
Fortuneatly being in the UK I don't have to pay for medications.