I am newly diagnosed with COPD after a flare in January. Aside from hyperinflation, my biggest issue is how strong my pulse is all over my body but I also get a really strong pulse in both arteries in my neck, so much so I can see it pounding in the mirror. I was wondering if anyone else gets this?
Thanks
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sinclair61
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I have been checked out by a cardiologist (ECG, holter etc) and he wasn't concerned. My blood pressure is normal and resting heart rate is usually mid 60s.
Only thing that came back was slightly high total cholesterol but, once again, the Dr didn't seem concerned.
I was just wondering if anyone else had this issue.
When I was first diagnosed I was hyper aware of every little thing. Any little pain, headache all became a symptom of something bad. As you have been checked by a cardiologist and everything appears normal perhaps there is an element of anxiety in this. All I know is that as I have learned more most of anxiety as gone and with it a number of my symptoms. This is the most honest answer aI I can give you.
The thing is I am not really anxious. I have pretty much come to terms with the situation and I am trying to make the best of it. But there are a few symptoms which don't seem to add up when compared to my functional status. I can walk for hours on end, I can do a 5km run, cycle 30km in a hour. The only time I really get SOB is climbing stairs and even then I could run up 5 or 6 flight of stairs without having to stop. Walking them seems a far bigger issue.
What is confusing me though is that I get hyperinflated at rest and have trouble getting air out. Sleeping is also a problem as a result. That along with the strong pulse all over. I'm not particularly anxious about them but I am just intrigued to know whether these symptoms are to be expected.
Have you tried purse lip breathing? I am sorry but never come across this before. I do a lot of fitness and I use Purse lip breathing to prevent hyperinflation. I can run up stairs but you always take in more air than you put out, PLB stops this. I also practice this at rest. I also use diaphragm breathing which helps expel excess air. At times it a matter of finding what works for you. I have never come across the pounding pulse before except in either a heart or blood pressure condition and lastly in Anxiety so you are a little bit of a mystery. I hope you find an answer because it would be very interesting to know.
I regularly use purse lip breathing. But its so draining doing it all the time. Is the fact I've got to do it so often a sign that I'm not on the right inhalers or is this just something I am going to have to get used to?
I am currently only on serevent. Would something like Sprivia help with the hyperinflation?
Hi purse lip breathing as become second nature to me in many ways. However I have learned to do very soft in and out. I follow Donna Wilson's method with a slightly longer but softer blow out. I find it's less stressful. As for medications all I take is Fostair 100/6 one puff twice a day. I very rarely use my rescue Ventolin. I have only been diagnosed since Christmas I am stage 2 57%. I cannot comment on what could help you medication wise as what works well for one does not for others. I would talk with your respiratory nurse or GP. Do you own a pulse oximeter because a record of your saturations may help.
Also, forgot to ask - is it normal for a course of oral steroids to reduce hyperinflation? I found I had no hyperinflation whilst on them. Surely, that would then suggest it is inflammatory rather than loss of elasticity?
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