Permanent is a long time but ten years isn't bad. Along the way NOT having AF allowed me to have a life saving caner op which may otherwise have been refused so for me it was a life saver.
12 months (almost) and it's been worth it for that. I'm sure AF will return at some point, but who knows, maybe not.
In the mean time I will live as healthily as I can , shed the excess weight (there is a lot of it) and try and reduce my AF burden .
Hopefully if it does come back I will be in a better condition for the second shot.
My first ablation for paroxysmal Afib worked for 8 glorious symptom, and drug, free years.
I'm currently awaiting a date for a second procedure as I've had a couple of long episodes since last August and don't want to go into persistent Afl or afib.
My guess is that there are many, many, people out there who had sucessful ablations and are blissfully unaware of this forum. Much as I was after my original ablation. Once it had worked I simply got on with life unaware of any "bullets" I may have dodged.
I think it also depends on each person's lifestyle choices. A person who is on a very clean diet, and exercises regularly, and avoids anything that might trigger afib is more likely to stay Afib free. But people who think that because the ablation was successful that they can now go back to their old lifestyle, these will suffer the consequences.
3 years now but it is a reprieve not a cure. Also it is not always as a result of poor lifestyle choices. I am doing what I have always done and with EP approval. I do tend to get tired of some people thinking that AF is always a result of poor choices. It is not!
I think people often want to believe that life is inherently fair. That we get what we deserve. It makes sense to us when someone who smokes a lot gets ill, same for people who overeat or under exercise. I think it helps give us the illusion of control in an actually unfair world.
You only get one life/body so you should look after it. But sometimes bad things happen despite your best efforts. Fortunately I think the majority of people on this forum are more supportive than judgemental. When they talk about lifestyle improvements it is usually intended as advice, not blame.
On this forum you may be right. Generally....now that's quite different....in my experience anyway. More education needed I think even amongst the wider medical profession.
There is a lot of truth in Bob's view that those who are 'cured' do not post on this forum, only those that have problems. Do not be downhearted by the negative events - what would you do if it didn't work fully? We have to accept the NHS figures that talk of percentage 'successes'. Many who have had successful treatment for AF have never even found this forum!
Last time mine was in AF was Xmas 2016 and went back after a week and tuch wood been ok now still just on Apixaban no other meds for heart so hope it Carrie on
I had SVT. Was on train, became extremely weak on verge of fainting and extreme warmth. Limp wrists.....opened coat and auto dialed my son. Not sure I could walk. He met me at LIRR stop. I asked him to get me a cadbury bar (Not diabetic) but likely dehydrated and had a lot of etoh that night at play Imbible and not enough water. The candy helped (not diabetic). Went to a cardiologist for stress test...fine. Wore 10 lead monitor. Had 2 calls asking me if I was just jogging etc. I was standing at kitchen counter feeling fine while making coffee. Wore monitor for 30 days. DX SVT. I had an extra "conducter" near the middle one in heart. Sometimes blood heading back would stop there and move on. Sometimes it kept looping around with long delay moving back. To avoid stroke etc I wanted it "fixed" so had the ablation and take Sotalol. Was sleeping 15 to 18 hrs a day, hair falling out, lost 30 lbs...skin n bones...sagging skin on thinning bones. I was hospitalized about 5 months after procedure with diverticulitis (have hx). On my own I figured out I was not absorbing nutrients and starving. Sotalol slowed down everything and made me sleepy. Instead of 80 mg 1/2 AM and 1/2 PM, I break it into 3 parts. Use Diatermateus Earth 100% food grade daily to scrape out diverticula (it worked). Gained 10 lbs back. Still weak and tired but less so. I'd love to stop the Sotalol but am worried the SVT will return. I did wear a monitor again for a few weeks. Results were "not remarkable" but not fine. Want to do more but am too weak.
Sounds like you got some really good help when you needed it. I had diverticulitis twice and it’s a rough thing to have. Zero energy to do anything but breath with that. It gets better.
Thanks April. This was my 3rd episode of diverticulitis n sigmoid is damaged plus very narrow colon. Check out diatomaceous earth 100 percent food grade. It helps clean the waste stuck in diverticula. Digestion begins in the intestines....was able to absorb again. I think the Sotalol is adding to fatigue. Recent Rx had additional warnings 're driving, using machinery etc. Want to stop taking since I was ablated. No real research it seems. Did you recover or have surgery?
I recovered both times but my goodness-I thought the drugs for diverticulitis would kill me. I first had diverticulitis from swimming in a West Virginia lake. Once you have it -you tend to get it again.
A-Fib was exasperated by a steroid I was given for seasonal allergy symptoms. I have only been to the hospital twice with A-Fib. I have flutters at times now but no A-Fib. Nevertheless, I am on Pradaxa and Dilacor.
The diverticula pockets are still there just no longer infected. Important not to become constipated. I had a diverticula perferate. IV Rx in ER. Those pockets never go away unless I have sigmoid section removed ......6 mths to heal n have that bag. No way!
Ouch!! That’s why you were in ER and hospitalized for months!!!! So sorry!!The diverticula pockets are still present in mine. I can not have typical colonoscopies I’m told . They do something similiar but are careful. Thank God they are not infected. I avoid tiny seeds as much as possible but have had them and noted nothing. Will take D-earth. Thank you The cure is to section that off!!!I know someone who has the “dreaded bag”. Doing well. Flys with work related trips and 15 years in with it.
If you live long enough-seems like something comes along to whack at you. Now it’s A-Fib!!!
The biggest indicator of success is WHO does the procedure - as recently highlighted by some posts on here - this has also been borne out in fact in a US study. The experience of the EP is vital.
Yes. I went to EP at St Francis (the Heart Hospital). Don't know if that extra node ablated can return but I think once it's ablated it's gone. Not understanding why I need Sotalol. Aprilbday, unless it's the hx of diverticulitis that's causing fatigue, weight loss and brain fog.
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