Put a temporary hold on my Dulera and... - Lung Conditions C...

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Put a temporary hold on my Dulera and Spiriva

patrickd72 profile image
7 Replies

And Albuterol. I have SOB on them, off them. I have been on/off the Dulera since Jan. I stopped taking in the past when this all began in Jan because I did not notice a difference. I started again a couple weeks ago per my GP, and don't feel much different. On Spiriva almost a month, not much difference. Maybe after I first use it, then it's like I never took it. Maybe the same could be said for Dulera. Once lasts 24 hr, one 12 hr. I just don't know sometimes. My SOB already out of proportion to my PFT's not to mention the meds feel like they do very little. Prior to all this I rarely used Albuterol, and when I did it worked wonders. Now I use two meds daily and it's like the difference is so small, if at all.

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patrickd72
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7 Replies
jackdup profile image
jackdup

I feel much the same way and do find it frustrating as so many seem to get a real benefit from their inhalers.

knitter profile image
knitter

Hi Patrick....just keep an eye on your breathing if you decide to take an inhaler break. E

Nearly everyone is genetically different and reacts differently to medications....there are quite a few inhalers that disagree with me but suit others well.

Take care and let us know the results when you have a CT scan.

patrickd72 profile image
patrickd72 in reply toknitter

Knitter,

Thanks, I am keeping an eye on my breathing. I ca always restart if necessary. CT on Wednesday.

P

Dmactds profile image
Dmactds

I'm on Spiriva once in the morning and was on Symbicort in the morning and evening but now only in the morning for the past week or so and same as you, don't feel any difference as far as ....., well..., anything.

Overall, due partially to the cooler weather I'm sure, my general sense of well being has returned and I feel much better though still short on breath, but not as much week by week and some abdominal muscle definition is better.

I'm convinced at least part of my problem is having allowed my midsection to become lax and out of shape so am paying particular attention to eating less, shrinking my stomach, doing my pursed lip breathing and getting more exercise through walking and yardwork. It seems to be working and making myself get out of breath seems to improve my abilities from one day to the next.

patrickd72 profile image
patrickd72 in reply toDmactds

I think this is day 3 off Dulera and 4 days off Spiriva. I don't feel any different. Yes, still have SOB, then again I did on both inhalers. I can always start them up again if I feel the need.

challny profile image
challny

Hi, I also wonder if my inhalers are working at all. I usually wait until late in the morning to use them, and it never seems like they give me much of a boost. I quit Symbicort for about a week just this past week and just used Spiriva. Seemed like there was no difference. I usually don't notice any help from Ventolin, either. My breathing is not that bad, but it's not great, either. I just went to my pulmonologist about 2 weeks ago and registered 71 percent FEV1. She thought everything was brilliant. I just wish I got more of a boost from my inhalers. I often wonder if some other type would work better. But I know that the Spiriva/Symbicort combo is very popular with docs. One thing I will say is that I've been going to pulmo rehab for about 4 months and I do think that helps. I also take a Xanax in the evening, and I think that helps a lot. It relaxes me so much. But my pulmo said she would NEVER give those to me because they interfere with REM sleep. I get them from my GP, who says he believes they help me, so he gives them to me.

Stumpy55 profile image
Stumpy55

Hello Patrickd72, when I first discovered I had copd quite a few years ago now, my medication was a lot milder to what it is now, and over the years I've tried different pumps and various different types of medication in tablet form before going on to a nebuliser which is what I'm on now. But along the way I've had to change to different meds because they haven't suited me and caused a reaction. So you need to keep Intouch with your doctor. Once you have your C.T scan then that will paint a clearer picture, so hang on in there. Please keep Intouch with us? Good luck to you.✋️😊

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