Hello and welcome to the forum! Have you ever had an exercise ECG? As you struggle with stairs this could be a relevant test. Personally I believe resting ones are of limited value as mine was normal despite four severely narrowed arteries. Do you mind me asking your BMI as this can sometimes have a major effect.
No weight worries then - maybe a little under even. I think your symptoms may be related to your sympathicotonia but know next to nothing about this. My suggestion would be to call the BHF nurses on Monday for advice as obviously your quality of life is badly affected. Let us know how you get on.
It's perfectly likely that the adrenaline and anxiety causes your symptoms. The brain gets anxious, which causes a flood of adrenaline, which causes symptoms, which in turn causes anxiety - it's a vicious circle.
I think you should accept the findings of your numerous tests and your doctor's reassurances that they have not caused any permanent damage.
I wish you all the best - anxiety is a very difficult thing to live with.
Since summer I had been experiencing blackouts, without any warning at all.
I had so many tests done. I had 48 hour blood pressure and heart recording gadgets attached to me. Absolutely every test came back clear. I don’t smoke or drink and am never poorly so it was a total mystery.
Just before Xmas I had surgery to have a loop recorder inserted in my chest. This picked up that my heart was totally stopping and I had emergency surgery to fit a pace maker.
Without the loop recorder and the home pack sending my heart information to the hospital every night, my condition wouldn’t have been picked up.
Maybe you could request a loop recorder ??? I’m now recovering but feel my condition has finally been identified and fixed and I can resume normal life again
I had similar symptoms and have been diagnosed with myocarditis. I think it's quite a hard one to diagnose, it was their initial suggestion but they were only able to confirm it by running two cardiac MRI's some months apart and seeing the change in inflammation. The reason I was sure it was a heart thing is that all my initial symptoms were only happening when the heart was beating faster, sitting down at rest I feel "almost" fine. I do now have heart failure though
I have a mitral valve prolapse,they say within normal limits but I have been feeling like yourself, nearly passing out sometimes,tired fatigued and feel I cannot pursue normal living some days. I am having it checked on March 2nd. I have bad palpitations also. I,ve never had high blood pressure either.
Yes ,very much the same as you! I do my housework in the morning and feel worn out just after an hour, tired breathless and fatigued. I was always doing something before this but tend to sit and watch television more nowadays.
I see you have a mitral valve prolapse too, I can,t help but feel this could be the reason why we feel the way we do. I don,t know why they have grades for replacement,they should base it on how we feel. You are a lot younger than me so valve replacement has a shelf life before it needs replacing again.
Hi. I am a 37 year old female. I am a bit similar, although walking or going up the stairs does not trigger severe symptoms in me (maybe only on a bad day). Mostly for me it is things like doing actual exercise e.g. running, cycling. Anything I used to do easily I before I have to avoid now because of these symptoms. It started many years ago and got worse over time. However in the last 2 years it`s gotten much worse than ever before. It does feel similar to a panic attack or anxiety but I don`t understand why it is only triggered by exercise...I also have a mitral valve prolapse (congenital) and apparently very mild so no treatment required. I have had stress echo, ultrasound, 24 hour Halter monitoring. I wish they repeated the Halter though...I can sympathise with you. It is so frustrating not to know what is happening with your body. I just wish I new what the issue is...
Hi. Did you have any progress at all with the diagnosis? Have you ever been prescribed anxiety meds like Propranolol? My GP prescribed me some once but I never took them . They are heart meds apparently as well, they slow your heart rate
Currently i am waiting on this covid 19 situation to calm down and get another medical consultation.
I take heart rate slowing meds(beta blocker), but they make no big difference.
Hi! As I got older it got worse, I was active but get very tired . I still walk a lot but now have arthritis in my knees so I suffer with pain at the end of the day something else to add to the misery.
I started to get palpitations when I was 28,now 73. For years they couldn,t find anything wrong. I have read so many people with mitral valve prolapse which I have! Could there be a connection, I have always felt fatigue and breathless. I,m ok apart from fatigue, get tired quickly and aches and pains. I have Supraventricular tachycardia,mitral valve prolapse within normal limits. All my life I thought it was my nerves causing all this,it made me quite depressed at times. I worked and brought up 3 children. I sympathise with you because it does affect your life.
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Can't get heart rate up
getting worse
My mircovascular disease is getting worse 
Just getting worse. 
Should we be warned if they see we getting worse 
