TO: abwilli78
Wow, I have been searching on here for two days, and I finally found someone else having the same issue. My eleven year old just had his cardiac ablation last friday, they couldn't make it happen, so unfortunatly it didn't work. BUT, they also made and error and told us they (1) the wrong size cathader in, and (2) he accidentaly entered the artery instead of the vein. So.. for the rest of the day his right foot was ice cold, they could only get a pulse using a dopler. he was in alot of pain both from the site, and his foot, teh whole time we were in the hospital, yet they release him anyway, saying they were sure it would be fine.. that as long as there was some blood flow it would be ok. Well...3 days later, he is still in a ton of pain, foot has better color and all, but he can bearly walk on it and he gets shooting pains, He has also complained of it being cold and feeling like it is wet.
I am so scared this could be something worse. I am going to call in tomorrow, but I have a feeling tehy are going to tell me the same thing again...It is so frustrating!!! I am curious about how you are doing and if you found any relief. Thanks, Crystal
I had ablation surgery last December for A-fib. Procedure took about 8 hours and by March I was off all my heart meds. I feel great except that when I do anything the least bit strenuous, I get so out of breath. Have been trying to hike with my husband and he has to stop several times and wait for me to catch my breath when we're climbing. But apart from that I've had no issues whatsoever and am thrilled with the results as I could not tolerate the meds they had me on before. I'm so sorry to hear about these serious issues some of you are dealing with. If you're looking at a repeat procedure, I'd advise you to find a different doctor.
Had my 3rd ablation done June 23rd 2011. It was a success, i had a difficult pathway behind the heart. My question is i still have chest discomfort and a few PVC'S. Dr. said not to worry because the ablation in very invasive and i will have side effects for the next 3 months sometimes up to a year.
I was suggested an ablation, I am 48. I decided not to do it. To me, any time you deal with your heart you are at risk. Doctors do not know everything so when I read your replies I believe you. Good site is heartracing.com explains risks and benefits in detail. If I were yal I would get a second opinion, find a good doctor who listens. Don't let ANY doctor intimidate you!!! I have worked with doctors for years and they are only human. There are okay doctors, greedy doctors and great doctors, keep looking even if you have to drive further. I have driven a 300 mile distant for some specialists and it is worth it. I understand why you did the ablation, I live with SVT. I want the surgery but am too unsure right now. I feel for all of you who have problems with this. You are all in my prayers because you deserve it.
Sound like Pulmonary Vein Stenosis from the ablation: http://adventuresincardiology.com
I had an ablation for incessant PSVT in June 2010. It's been four months. I still have PACs, tachycardia and episodes of PSVT. They are not as bad as before the ablation but still happening.
For the first 2 months after I couldn't do a thing. My heart would get stressed out, pound and get tachy from moving on the couch. I had trouble just breathing. Felt like I was suffocating laying still. It was torture. I could barely go to the bathroom w/o passing out. (I was not like this before the ablation.) I was so miserable I thought I was going to die and I was okay with that.
Everyone is different when it comes to ablations. The side effects are dependent on where the ablation was done, how many burns were made, what condition your heart was in before, your age, etc.
The only definitive thing I can say: ablations are not a walk in the park. You will have symptoms, some of them very unpleasant for MONTHS afterwards.