Pacemaker recipients: Looking for support from others
I am coming on a year post op having a pacemaker placement for bradycardia. I would be interested in a support group with the same concerns. I think a support network would be so beneficial.
Interested in more discussions like this? Go to the Pacemaker & ICDs Support Group.
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@balubeje
Concur,
Colleen can you set it up.
I had a ICD/Pacemaker inplanted in 2006 at Mayo Jacksonville. I have been through so much with it I could fill pages. My experience and it is both bad and good. It now spans almost 20 years and on my 3rd one. Bottom line, would I have it implanted if had to do all over, YES! I am only alive and writing this because I had it implanted.
I learned so much from Pace Clinic at Mayo, my Electrophysiolgist, cardiologists and my own research. I also go to the manufacturer of my ICD/pacemaker (Boston Scientific) which is also a great place for research and will also answer your questions about your specific product.
Where I used to worry about having it I now smile knowing I have it.
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2 ReactionsGreat idea for pacemaker group!!!!
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4 Reactions@gut Yikes. Sounds like a lot of medicine. Try various vagal maneuvers (can be found on the internet). I'm 81, male, with ocasional AFIB and tachycardia. I'm only taking 25mg of metoprolol daily, and have yet to have to take any more metoprolol as a "pill in the pocket" if an event occurs (HR over 120 bpm). Instead, the vagal manuever has worked for me. Good luck.
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2 ReactionsMy mother had ALZ (early onset). I know how difficult it is to deal with. I think your concerns about a pacemaker for your father are right on. A discussion with his GP as well as the cardiologist would be helpful.
Glad your insulin pump is doing its thing. We can do so much more "living" with the help of our electrical friends. 🙂
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2 ReactionsYes, this is very helpful. I was inquiring due to my father’s situation.
He is 87, has CHF, with CKD, an aortic aneurysm (under 5), multiple PVCs, hypothyroidism and ALZ. We’ve been told he may need a Pace maker one day. Quadruple bypass in 2000 and 4 stents since. As we anticipate it, we are concerned with his cognitive ability to leave the device alone for healing. He is obsessed with any little thing on his body and picks at it constantly, asking what is this? Moles, skin tags, etc. We fear he would become highly distressed with something under his skin, he could not understand what it is or remember what it is. Thinking of palliative care going forward.
It’s awesome the device is working for you! So great to see this! And, I wear a Medtronic 780g insulin pump! Love it! It’s changed my life!
I have had my pacemaker for almost 2 years. Very simple procedure. You can feel it under the chest. The only visibility to others is a small scar that fades with time. Healing is variable, I assume, with different people. I was given a sheet that outlined things to do and not do with a timeline. Initial healing takes a couple of months. I do strength training including deadlifts weighted squats and bench press. I did nothing for 8 weeks. When I returned to the gym, I was scared but I took everything very slowly starting with basic body work. When I began weights again, I started very low. I have a trainer so I was supervised but the guideline has always been to listen to your body and proceed gradually. For the most part, I don't notice the pacemaker. I do get discomfort sometimes but I've never had pain. I also do Zumba/occasional Yin Yoga and have never had a problem.
My reason for a pacemaker was bradycardia. I had all the classic symptoms: fatigue, shortness of breath, little dizziness after some exercises. My heart rate was 31 when I went to the hospital. I don't think it is an exaggeration to say that the pacemaker gave me back my life. My pacemaker is a Medtronic. They have a good website for patients and an excellent 'call with your question' line. I assume other manufacturers have resources too.
Hope this helps
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4 ReactionsCan anyone describe what the pace maker is like under the skin in the chest! Can you feel it? Is it visible? What about healing?
I am 77, a woman with afib and flutter. I take 180 mg diltiazem in the morning and if a fib strikes (always when I am resting or asleep) I take a rescue 30 of diltiazem followed up in an hour if it is not successful with 25 of metoprolol. Not sure what to do if that doesn't work as I hate going to the ER.
Suggestions?
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1 Reactionaramsaier, My caregiver at Mayo for psychiatric care and medications prescribed an anti depressant some time back. It was going to affect the electrical signal to my heart and increase delay.
She checked with my heart failure doctor and EP to make sure they would approve and did. Really doesn't affect your pacemaker but the electrical signals to your heart and like mine would increase a delay in on the signals.
Please check with your EP (electrophysiolgist) to see if it will have any affect on the electrical signals from heart as everyone is different and what might not be a problem for me could be for you. My heart is paced at 70 bpm to help with PVCs normal pace is around 54.
I did improve my mental outlook when I got the prescription. I was suffering from PTSD which developed into an anxiety/panic disorder which made doing anything socially very hard. And what caused my PTSD? Several years ago had 5 ICD shocks over a 24 hour period. Medications and reprogramming ICD/Pacemaker along with the anti depressant helped me out of it. Had occasionally problems since then but lately (and will knock on wood) been without issues.
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2 ReactionsI would like to know if anti depressants affect a pacemaker
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