Most Recent Messages in Checkups & Settings
Comment posted by noodles69us on 2007-12-08 09:57.
I had my pc check 2 weeks ago and told them I wasn't happy with the way things were going and that something had to be done. If the Doc. or the Teck. would have listened to me after I told them how my heart would race with going over bumpy roads or just walking they should have known the settings were wrong. I shouldn't have had to go 3 months with chest pain and a raceing heart that long. To make a long story short, she...
Has anyone had their settings changed for their AV Delay and Have you felt a difference? What is AV Delay and how can it make you feel worse or better?
I haven't posted for a long time. Had my annual PM check last week. Since my last check I have had a number of days where I get 5-6 strange episodes. My cardiologist thought they were vasovagal attacks. Anyway I expected that the PM check would not indicate anything as it had in the past, but this time it showed a number of strange beats, I'm not sure what, but the technician was checking for noise and mentioned ectopic and fast beats. So I now have a devise called a remote assistan...
thanks to all who suggested the ep follow-up. i actually saw the medtronic tech and with one or two clicks of his computer attached to the blue "hockey puck" i was off and running with the symptoms gone.
thanks to all of you and this is a wonderful website especially to us "newbies."
I have had my St, Jude model 5376 about 2 years with no problems. In late Octorber I went with a friend to a hospital where she had an MRI. I was sitting in a room about 30 feet from where the machine was, the door was open.
I was a little concerned, it happened that a couple days later I was scheduled for an in office check of my pacemaker, every thing was OK, they said.
But days later I unexpectedly passed out while sitting in a chair talking with some one.
I just wanted to let everyone know I had my 1 year check-up. The doctor asked me how I felt, tested the pacer, asked if I wanted any settings changed. ( I have spent more time analyzing the pacer than he has). He then told me my battery was good for 5.7 to 7.7 years, and told me to come back every 6 months.
It was great to finally have some good news, and not to have to fool around with more drugs
I went this week for my every-couple-of-months check in with my doctor. I had my pm installed in May of this year. I have tachy-brady syndrome. I'm becoming unhappy with my doctor because he isn't giving me answers when I ask. I asked this visit if I could get a full interrogation to learn how much/often my pacemaker is working for me. He asked me why -- that "curiosity killed the cat." What kind of answer is that? I just meekly said, I would like to know. I didn't even k...
can anyone tell me about settings.i have a dual lead st jude pm and it is set as low as poss as im sensitive to higher settingsbut i feel as if my heart is being squeezed on each beat. i also feel lightheaded on standing and have fast heart rate after eating and exercise tolerance is poor. i have had the pm for five years and only had these symptoms recently. i have a moveable pm and am waiting surgery for deeper implantation and am due for a pm check up soon but they are not very helpful at th...
Just had my first 3 months check of biventricular pacemaker.
Performed by St. Jude Medical technical consultant. Went very good. I told him I feel tired most of time and he said he would see what he could do. He made adjustments and then told me the following:
"Prior to 10/29 checkup device was not pacing in ventricular chambers now is pacing both chambers."
I do think I have more energy and hope it continues to improve.
Best regards to all, b...
Going for first three month checkup of StJude Frontier II Model 5586 biventricular pacemaker. Know hardly anything about the device. Understand the checkup done by St. Jude technician with nurse from Cardiology Lab. Don't seem to have any problems with device. Usually feel tired. Has anyone got advice on what questions to ask?
It has been a month since my Medtronics Adapta dual lead pacemaker was implanted. I go back next week for my first month checkup.
I have noticed a significant decrease in the benefit I was receiving for the first couple of weeks after implantation.
Now I'm feeling tired and more short of breath again. I think I read somewhere that pacemakers might need adjustment after the scar tissue that holds the leads in place is formed. Maybe that's what is going on.
I had check up for my pacemaker. The ep person said I was using my pacemaker in the upper chamber about 8% and lower chamber about 100%. what does that mean to me. I forgot to ask what those numbers mean. Thanks, Karen
Hi PM pals,
Well, I am 5 weeks after surgery, and had my first check-up today. Or should I say, tried to? They were able to tune my pacemaker to a different setting, and could tell that everything was working, but they couldn't do a "interrogation reading" because I was so shook up, my heart rate went up to 113, I said to the Tech, please take it off (magnet) I have to sit up, she said "Janice, I haven't even did anything yet. That is your own heart rate." So apparently, they can'...
A while back I posted that rough roads were causing my PM's rate response to kick in while I was driving (an 18 wheeler). Today I went to the PM clinic and they changed to sensitivity from medium high to medium low.
Also noted was I had went for 4 1/2 months without any bouts of a-fib then had an almost 2 hour episode yesterday morning (I woke up to it) and one that lasted almost an hour this morning. This mornings bout had happened without my knowing it because I was asleep. I wonder...
Hello everyone I have a great dilema and I need some opinions. I have a pacemaker since 2002 and ever since then my life has been a total blessing. I have felt great other than having to deal with my rate response when I am driving. It activates when hitting bumps and makes my heart race. Well anyway it helped me when I was playing basketball so I never really complained to my cardiologist. Well because of insurance purposes I was forced to switch doctors and cardiologist. The new cardiologist s...
I know probably a lot of you have had phone checks before. I am scheduled for my first one Oct.30 and everyday it makes me more nervous. Does it feel any different that when you go into the office? My wonderful husband of 31 yrs. says he will take off work and be here when they do it if that will make me feel better. But I don't know why it is bothering me so much. I just somehow feel it is not the thing to do. Is this a normal reaction? Has anyone felt like me or I just being paranoid? Thanks...
hello, i'm new to this site. never knew it existed. i had my first pacer check. wow! kinda weird, the rest of the day i kept feeling a small jolt from time to time. i'm 10 days out of surgery. didn't know if maybe someone else has experienced this. please let me know if you have any answers. all i hear from the doctors is "it can't be shocking you, you don't have a defibrillator." please help!
I went this morning for my 3-month checkup and all seems to be OK. During the test, he (electro-physiologist) ran some diagnostic things on the computer, including speeding my HR to 100 and dropping it to about 40. At the lower rate I felt very lightheaded and nauseous. It reminded me of before I had my PM.
Do these all sound like the normal parts of an evaluation? From now on, I will start with the monthly phone checkup, and he tweaked my PM to increase effic...
I've experienced multiple incidents where I had the fast heartbeats and the ICD did not register the incident. Finally, I was at work as a teacher, went to the clinic when I felt problems. The nurse called 911 because I had a heart rate of 320 which was documented with a 12 lead EKG by the paramedics. My ICD didn't register the incident, but I finally had a strip to prove my point that these incidents were happening. In addition, being in the hospital while they tried to get it back under contro...
i just wanted to update those of you who remember me. i was complaining of a full feeling in my neck and face. SVC syndrome was ruled out. my old EP wouldn't do anything else. so for 1 1/2 years i suffered with this. i couldn't even exercise i was so miserable.
i switched EP's. he said i have pacemaker syndrome. he changed my settings and the full feeling is gone. he turned my rate smoothing off, lengthened my AV delay and now i am only going to pace in...