Hard to breathe - Does fibro affect the lungs?
Posted , 7 users are following.
My fibro symptoms came 2015 and was dx 2017. Ever since then I've had terrible asthma and now mild sleep apnea.
I have been to multiple heart doctors and a pulmonologist. I've been through a plethora of tests and they all come back normal (for which I'm grateful) BUT I still feel like it's hard to breathe!! Along with the breath issues comes PVCs (heartbeat skips - which also started w my fibro). I was told the CPAP machine would make my breathing better but it hasn't helped.
It's driving me nuts!! It comes and goes. My chest will feel heavy. Sometimes so heavy I use my rescue inhaler and go to the ER for steroid shots and breathing treatments that really don't do anything other than make my PVCs worse.
What else can I do? Who else can I see? Does anyone else experience this at all? Is it the muscles? It's not pain making it hard to breathe, either.
Any advice would be amazing. Thank y'all.
0 likes, 6 replies
Jeanniep Hayhue
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Magpie2me Hayhue
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Hayhue Magpie2me
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DebbieHurts Hayhue
Posted
I don't know the answer either, but my dr is giving me all tests, too, because I am having low oxygen all the time. So low I have to carry around an oxygen machine all the time now. I did have asthma but not that bad, and I have had Polymyalgia ,too, but fibromyalgia has been with me for 30 years. I also have to sleep a lot after being somewhat active. Weird.
Hayhue DebbieHurts
Posted
My oxygen level is actually great it was 102 at my last pulmonologist visit last week that's why I'm so confused. I hope the machine isn't too much of a hassle for you and that it helps you feel better!
Flutterbie57 Hayhue
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I always have to stop and admire the view. Its amazing how much more I see along the way nowdays.