What is Pacemakers
A pacemaker (or artificial pacemaker, so as not to be confused with the heart's natural pacemaker) is a medical device which uses electrical impulses, delivered by electrodes conta...
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A pacemaker (or artificial pacemaker, so as not to be confused with the heart's natural pacemaker) is a medical device which uses electrical impulses, delivered by electrodes conta...

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calling all pacemaker people
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Calling all of those living today with the comfort of knowing that they are protected by their pacemaker of ICD. How is it going???
I am doing fine and forget that I have it sometimes. Maybe we should do like we have decided to do on the heart failure forum and share why we have a device, what kind it is, how we are doing with it, etc. to get some discussion going. What do you think??? Shelly Posted on 01/30/09, 04:01 pm |
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I hardly ever think about my pacemaker anymore. Except to be thankful I have it.
I have a St Jude 5816...implanted in July of 2006. Shelly, tell us about you. Sue
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I forgot to say WHY I have it....bradycardia, AFib and long sinus pauses.
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I have a medtronic biventricular pacemaker with an ICD. I had heart failure in August 2005. After six months of treatment and wearing a device(external defibulator) called a Life vest I had an internal pacemaker and defibulator implanted in January 2006. My pacemaker has improved my heart function dramatically. Mine works by synchronizing the beats of the left and right sides of my heart and making it work more efficently. The left side of my heart is severly damaged from the heart failure and I have a left bundle branch block so the left side gets no signals as to when it is supposed to beat. When it beats on its own it is random or in reaction to the right side beating. The study that was done to get these pacemakers FDA approved was called the "miracle study". The last time I had an Echocardiogram the tech who did it has been doing my Echos since the first day I was in the hospital. She said "this is why they called it the miracle study" I am so thankful. To think, If this had happend to me 10 years ago, I would either not be here or be VERY ill. Tell me some more about you....
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Hi--I received a Medtronic ICD in October of 2007- I was 46 years old. In July of that year- they told me I had idiopathic heart failure - EF 29--VTACH and AFIB and my heart was enlarged - cardiomyopathy. I had a four hour ablation among other tests---They could not find a cause - they think I was born with a weak heart and no one caught it.
While I know my ICD protects me from sudden cardiac death, I am still anxious and nervous about all of these problems. I work-- and I try to function normally as a wife, mom, etc. But, I think to myself--should I be doing all of this--Will my heart just conk out? I am always tired. I still feel like I need some help. I am really scared!!! No one seems to understand. I hope all of you are well. Thanks for listening HUGS---Michelle
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Yes, it is a reason to be thankful. What a wonderful outcome for you.
About me...I've had arrythmia, atrial fibrillation (causing sinus pauses), and borderline bradycardia for most of my adult life. But it was VERY intermittent and sporadic. I could never get any test or Holter monitor to show it. I was told my heart was in perfect shape but probably had PVC's or something similar. Sometimes a whole year would go by without symptoms. Anyway, I had serious lung surgery in July 2006. Valley Fever (coccidioidomycosis) destroyed the middle lobe of my right lung. After a lobectomy and while in ICU the alarms kept going off on the monitors. The medication stopped the A Fib but made the bradycardia much worse. My heart rate was in the high 20's. Anyway, on the 3rd day I had a pacemaker implanted. So, I went into the hospital thinking I probably had lung cancer and left the hospital a week later with a "no cancer" diagnosis but with a pacemaker. A very confusing time to say the least. Actually, I was happy to have a confirmation of my heart irregularities after all those years. I knew I wasn't imagining it. And I no longer have any symptoms at all! I'm very fortunate to not have any cardiac problems except an "electrical" malfunction. They don't even know what caused it, as is often the case. Anyway, I didn't mean to ramble on. Take care,, Sue
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I'm sorry, Michelle, but when I replied to Shelly your post wasn't up yet. I don't want to seem like I just disregarded your concerns.
This forum is a good one but not very active. Have you tried pacemakerclub.com ? They are much more active...many people post daily. Just a thought. Anyway, I'm sending hugs and prayers to both of you, Michelle and Shelly.... Sue
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I have a Boston Scientific Biventricular pacemaker with defibrillator. My heart functions like Sb57. My heart failure was caused by cardiomyopathy & a virus. The BVP was installed the end of November 2008 and I feel much better with it. I haven't had the ultrasound yet to see if heart function has improved but I feel like it has. My ef was 10% but doctors say that could very well go up.
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I know how you feel, Michelle. My heart function has improved a great deal, but I still have heart failure. Without the pacemaker/icd and all of the meds, I would out of luck for sure. I am tired Alllllll of the time. But I am still thankful for the quality of life I do have right now. I only can do about half of what I should be able to do at my age. It is scary and I understand.
My cardiomyopathy is idiopathic. In August 2005, my EF was 10%. It went up to 20-25% after about 6 months and the pacemaker. The PVC's kept it low until we got them under control. After that it went up to 35%, then 45%, and now 50% last summer. I suspect that is as high as it will get, but I am happy. I am so happy about this discussion. I hope we keep it up. Good luck to everyone and lets keep up the discussion. Love to you all, Shelly
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Shelly--mine is idiopathic as well--
your EF IS 50%?--that is awesome-- really great- it sounds like you've got a handle on this condition I will look for your postings and seek out your advice WOW!!!! Michelle
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I haven't been on here for sometime and never get the emails that people have posted on this board. So I'm sorry it's taken me so long to respond.
I have a medtronic dual chamber ICD this is my 3rd. I have Ventricular Tachycardia (Idopathic). I just had my first two shocks in May 08 and feel very blessed to have had the device so safe me. However I have been scared ever since the events. Anxiety etc. Soooo michelle I just want you to know it's totally normal and if you would like more info on how I deal with all of this let me know. Since the last implant I've also had pain in the area of the device implant and irritation in the middle of my chest that is painful with a cough .. I may need my device repositioned. They are thinking of putting it sub-pectoral. Anyway it's been a rollercoaster ride since May. I hope all is well with everyone on and I'm glad to see more activity on here.. Blessings Renee
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