Heart Rhythm Conditions – Welcome to the group
Welcome to the Heart Rhythm Conditions group on Mayo Clinic Connect.
Did you know that the average heart beats 100,000 times a day? Millions of people live with heart rhythm problems (heart arrhythmias) which occur when the electrical impulses that coordinate heartbeats don't work properly. Let's connect with each other; we can share stories and learn about coping with the challenges, and living well with abnormal heart rhythms. I invite you to follow the group. Simply click the +FOLLOW icon on the group landing page.
I'm Kanaaz (@kanaazpereira), and I'm the moderator of this group. When you post to this group, chances are you'll also be greeted by volunteer patient Mentors and fellow members. Learn more about Moderators and Mentors on Connect.
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Interested in more discussions like this? Go to the Heart Rhythm Conditions Support Group.
Hi Becky , I can't say I've heard that term exacting like your saying it , what I was told was I have hundreds of pathways that are basically rogue as they grew by themselves and don't belong there. And when they would go in and try and map the ones affecting the pacing of my heart. When they found a pathway that was causing an issue they would ablate it with either freezing or heat to shut off that path. Now I had so many their wasnt always time to find them all and also some were in places where they could not reach so ultimately the transplant was needed. So it may just be terminology but what your describing does sound similar. I know one doctor said I could have had over a thousand . The last effort they had was to try an MRI which typically can't be done with a pacemaker , since the magnetic waves would bounce off of it and make it hard to see what they wanted to see. Plus I was in a state that shutting off the pacemaker which was required ment a whole team of both Cardiologist and The techs for the pacemaker company were in the room during it. They tried for a few hours to try and determine where the bad paths were but it was unsuccessful. All I know is Mayo is a great place to be when you have the tought cases. And mine sure had them trying everything. So my doctors usually used terms like bad paths and I guess rougue could be a term to describe them also.
Hi,
We haven't had the pacemaker/defib conversation yet. I've mentioned exercise induced shortness of breath but didn't get much of a reaction. Will try again and am also going to look into talking to a Electro Physiologist cardio doctor. Thanks for your input,
Deb
Hi Dana,
Really appreciate you sharing your journey, this was very helpful. I have been feeilng that the next step will be an EP cardo doc and you have confirmed that I will need to find one soon. Thanks again,
Deb
Hi Deb, I suffered with Vintricular Tachycardia for about 10 years and had a pacemaker defibulater. I just want to stop by and say that the new symptom of shortness of breath is probably tied to the Tachycardia.
A brief history of me is that at first I was in the "until it does " category. I first was diagnosed with CHF with a IF of 5 % after a flu bug cased fluid around my lungs to enlarge my heart and so a pacemaker was put in as a precaution and i was put on Amiodroine and a beta blocker. I think it was coreg. So for about 5 years I had no issues that I knew of and one night the pacemaker had to shock me when I went into an arrhythmia where my pulse rate went over 200. Now I mentioned this because when the heart speeds up (that's what Tachycardia means) there is not enough oxygen rich blood leaving the heart to satisfy your body so you feel like your out-of breath. That was always my first symptom of an arrhythmia ( it's when the heart is moving so fast blood basically stops flowing) so the out of breath your feeling may be that your heart is in a situation I just mentioned of an arrhythmia. Now arrhythmias actually are common even in health adults but the difference is with a healthy system it usually only last a few beats and my be felt like a skipped beat or you may not feel them at all.
For me one test to verify if I was in an arrhythmia was checking my pulse. And if it seemed very fast or I could not feel it I knew to just relax sit down and let my pacemaker take care of it.
So my suggestion is to seek the advice of a cardiologist and if you believe it's electricial in nature a regular cardiologist may recognize it but that's when I was referred to an EP Cardiologist. EP stands for electro physiologist or a cardiologist that specializes in the electrical parts of the heart and most time that's where arrhythmia start, its a misfiring of the signals to cause the heart to beat. It gets out of sequence and they know how to fix those types of issues. I hope that helps and please let me know if I can help further. There are many was it can be kept under control so don't worry at this point. It could be something very easy to fix.
Blessings
Hello. I'm an 88 year old male who is still cutting his own firewood and swimming in a neighbors pond about 200 yards. Lately I'm really shot after each activity and have taken my heart rate, three consecutive times, immediately after. Runs from a systolic high of 119 down to 104 -- and a diastolic low of from 54 down to 44. The systolic high goes down a bit for each take and the low on the diastolic rises at the end of the 3rd take. Is this safely normal for my age ( I have and have had asthma all my life). eejj
I can't comment on your drugs, but your statement, "non life threatening, until it isn't" caught my attention.
Has your doctor considered an automatic implanted cardioverter-defibrillator (AICD)? Perhaps, that could be a "safety net" to prevent you from reaching the "until it isn't" scenario.
Hi, I have Non Sustatined Ventrical Tachycardia with shortness of breath (new symptom) when exercising. I've been told this condition in non life threatening, until it isn't. It seems my episodes are getting worse. I am female, 68 yr old in otherwise good health. I take a low dose aspirin, a beta blocker and a calcium channel blocker along with atorvastatin. Since the additon of these drugs the shortness of breath has started. Anyone with a similar condition? And any treatments that have worked? Thanks, Deb
Sorry Dana, I hate it when the stack replies to a post and it looks like you’re answering one but it’s attached to another. Sounds like you’ve been thru a a lot. Your ablations, may I ask a question, were they the normal kind or the Rogue Cell short circuit like in my heart birth defect? I’ve never met a person with the same defect because it’s a 1 in a million chance. I know my Electrophysiologist and his tram is waiting to go. Thanks for telling me of the misguided message.
It wasn't Me asking about ablation n it was Ted, but since you asked I've had somewhere between 8-10 ablation of both interior and external. I have had 2 pacemakers/recorder/ defibulator since my arrhythmia could kill me in a few minutes if the pacemaker could not get my heart rate down from the 200s in a short period it would shock me which it did on many occasions. But that's a long 10 year story. My longest ablation over 5 hours with 4 seperate leads in my heart and my shortest was about 2 hours.
Blessings
Yes, Please speak to your Doctor and follow his advice. Don't ignore.